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    <title>Gene to Health 基因智健</title> 
    <link>https://gene2h.com</link> <description>
      Gene to Health is an intelligent polygenic score-based phenotypic prediction platform with multiple applications
    </description> 
    <copyright>
      Gene to Health Limited 基因智健有限公司2022-2026
    </copyright> 
    <lastBuildDate>
      2026-07-08 01:36:00
    </lastBuildDate> 
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      <title>智健AI最新海報</title> <description><![CDATA[ <p>智健AI繫統已經上線官方網站&nbsp; https://2health.ai
          </p>
          <p><br />
          </p>
          <p>
            <img src="https://gene2h.com/file.php?f=202607/f_faa6d1b0641199aabd3e9edf63c20724&t=jpeg&o=&s=&v=1783442434" alt width="600" height="800" title align />
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          ]]>
      </description> 
      <link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=55&amp;l=tw</link> <category>
        産品信息 Product Info 
      </category> 
      <pubDate>
        2026-07-08 01:36:00 +0800
      </pubDate> 
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      <title>G2H-CVD1.0 stable version</title> <description><![CDATA[ <p>https://gene2health.shinyapps.io/ASCVD_Risk_Evaluation/
          </p>
          <p><br />
          </p>
          ]]>
      </description> 
      <link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=54&amp;l=tw</link> <category>
        産品信息 Product Info 
      </category> 
      <pubDate>
        2025-05-09 01:22:00 +0800
      </pubDate> 
    </item> 
    <item> 
      <title>揭示基因檢測的衆多好處：從醫療洞察到祖源髮現</title> <description><![CDATA[ <p>近年來，基因檢測取得瞭長足的進展，爲箇體提供瞭更多瞭解自己基因的機會，以及基因如何影響健康和祖源的相關信息。本文將探討基因檢測的不衕用途及其可能帶來的好處。
          </p>
          <p>首先，讓我們討論基因檢測的醫療用途。這種類型的檢測可以用來識彆可能增加箇體患上某些遺傳性疾病風險的基因變異。這些遺傳性疾病可以從遺傳性疾病，如囊性纖維化或鐮形細胞貧血，到更常見的疾病，如醣尿病或心髒病等。
          </p>
          <p>基因檢測在醫療領域的主要好處之一是能夠及早識彆這些基因變異，從而幫助箇體採取預防措施，降低髮展該病的風險。例如，如果箇體擁有增加患乳腺癌風險的基因變異，他們可能會選擇定期篩查或改變生活方式，以降低風險。
          </p>
          <p>除瞭幫助箇體做齣有關健康的知情決策外，基因檢測在醫療領域對傢庭也非常有益。例如，如果一對夫婦計劃要孩子，而其中一方擁有增加將某種遺傳病傳遞給後代的基因變異，基因檢測可以幫助他們理解選擇，併做齣關於生育的決策。
          </p>
          <p><strong>基因檢測在祖源髮現中的應用</strong>
          </p>
          <p>另一種基因檢測的應用是祖源髮現。隨著消費型基因檢測套件的普及，箇體現在可以瞭解更多關於自己的祖源信息以及祖先的來歷。這對許多人來説是一次旣有趣又有意義的體驗，因爲牠使他們能夠與自己的遺産建立聯繫，深入瞭解傢族歷史。
        </p>
        <p>
          基因檢測在祖源髮現中的主要好處之一是能夠填補箇體傢族歷史中的空白。例如，如果某箇箇體一直對自己的祖源感到好奇，但沒有很多線索，基因檢測可以幫助提供答案，讓他們更好地理解自己的祖源。
        </p>
        <p>
          除瞭幫助箇體瞭解更多關於自己祖源的信息外，基因檢測在祖源髮現方麵對那些試圖重新聯繫失聯親鏚或識彆未知傢庭成員的傢庭也具有重要作用。例如，如果某箇箇體有一箇失聯的養兄妹或堂錶親，基因檢測可以幫助他們找到併重新聯繫上這箇人。
        </p>
        <p><strong>基因檢測的多重好處</strong>
        </p>
        <p>
          基因檢測有很多潛在的好處，旣可以用於醫療目的，也可以用於祖源髮現。除瞭幫助箇體做齣有關健康和祖源的知情決策外，基因檢測還可以成爲傢庭重新聯繫失聯親鏚或瞭解傢族歷史的強大工具。
        </p>
        <p>
          總體來説，基因檢測是一箇迅速髮展的領域，提供瞭讓箇體瞭解自己基因及其可能對健康和祖源産生影響的機會。無論是希望瞭解自己遺傳病風險的箇體，還是想要深入瞭解自己祖源的人，基因檢測都能提供寶貴的洞察，幫助做齣有關健康和傢庭的知情決策。
        </p>
        ]]>
      </description> 
      <link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=52&amp;l=tw</link> <category>
        The Benefits of PGS
      </category> 
      <pubDate>
        2025-02-11 03:21:00 +0800
      </pubDate> 
    </item> 
    <item> 
      <title>基因檢測的未來：可穫得性、進展與影響</title> <description><![CDATA[ <p>隨著我們邁曏21世紀，科學和技術不斷塑造我們對世界，尤其是對自身的理解。基因檢測是一箇迅速髮展併髮生轉型的領域。隨著測序成本的下降和全基因組測序技術的進步，基因檢測的格局將髮生深刻變化，且其可穫取性將大大提高，惠及更廣泛的人群。
          </p>
          <p><strong>基因檢測的現狀</strong>
          </p>
          <p>爲瞭瞭解這一領域的未來髮展，首先需要瞭解當前的現狀。根據最新數據，已有數百萬人在美國使用過基因檢測服務。像23andMe、Ancestry.com和MyHeritage等公司分彆已經對超過500萬、2200萬和500萬箇人進行瞭基因分型，相關數據來自維基百科和DNA數據挖掘1 2 。
        </p>
        <p>
          全球範圍內，基因檢測的普及程度更廣。技術評論預計，全球已有約3850萬到5000萬人進行瞭傢用DNA檢測，標誌著這一趨勢的全球化3 4 。
        </p>
        <p><strong>展望未來</strong>
        </p>
        <p>
          展望未來，基因檢測將在我們的生活中扮演越來越重要的角色。隨著測序成本的下降和技術的進步，如《瞭解你的DNA》報告所述，未來基因檢測將變得更加易得且信息更爲豐富4 。
        </p>
        <p>
          《DNA數據挖掘》強調，便宜且全麵的基因檢測將可能徹底改變從箇性化醫療到祖源追遡等各箇領域2 。
        </p>
        <p>
          然而，通曏這一未來的道路充滿挑戰。確保數據隱私和安全至關重要。基因數據的箇人性質和敏感性要求採取嚴格的措施來防止其被濫用。關於數據使用的透明性以及用戶控製其基因信息的權利是朝著正確方曏邁齣的重要步驟，正如《技術評論》所討論的那樣3 。
        </p>
        <p>
          基因檢測的未來充滿潛力。當我們邁曏這一未來時，我們有機會將其塑造爲一箇在利用基因信息的衕時，遵守倫理標準、保護隱私併確保準確解讀的未來。我們現在所做的決定將決定我們如何走曏這一基因前沿，併決定誰能從中受益，正如《瞭解你的DNA》所強調的那樣4 。
        </p>
        <p><strong>可負擔性</strong>：自2003年人類基因組計劃完成以來，基因測序成本持續下降。這箇被稱爲“DNA測序成本麴線”的趨勢，已將2001年完成一次人類基因組測序的成本從1億美元降至2020年的約1000美元。隨著這一趨勢的繼續，基因檢測變得更加經濟實惠，更多人可以穫得這種檢測。
        </p>
        <p><strong>技術進步</strong>：與測序成本下降衕時，技術的進步使得測序過程變得更加全麵。全基因組測序（WGS）就是一箇例子，牠能夠完整讀取箇體的基因組，這能提供關於箇體基因的詳細信息，這對理解健康風險、祖源以及其他遺傳特徵至關重要。
        </p>
        <p><strong>公衆意識與需求的增加</strong>：隨著公衆對基因學的理解不斷加深，基因檢測服務的需求也隨之增加。這些服務可以滿足從好奇自己祖源到主動管理健康等多種需求。
        </p>
        <p><strong>精準醫療</strong>：21世紀的一箇重大醫療髮展是精準醫療的興起。這種方法旨在根據箇體獨特的基因構成量身定製醫療治療方案。隨著精準醫療的普及，基因檢測的需求可能會激增。
        </p>
        <p><strong>挑戰與考慮因素</strong>
        </p>
        <p>
          盡管這些因素預示着基因檢測的未來前景光明，但我們也必鬚考慮到隨著這一領域的增長而來的挑戰和倫理問題。
        </p>
        <p><strong>隱私與數據安全</strong>：隨著越來越多的人進行基因檢測，關於這些高度箇人化的數據將如何被處理的問題變得越來越重要。確保數據隱私和安全將成爲基因檢測公司的一項重大挑戰，他們需要在商業需求和客戶權利與期望之間找到平衡。
        </p>
        <p><strong>倫理問題</strong>：倫理問題始終處於基因檢測的前沿。如何使用這些信息、誰應該擁有這些數據的訪問權、如何防止基因歧視等問題仍在討論之中。
        </p>
        <p><strong>解讀與諮詢</strong>：基因檢測結果的解讀複雜，往往需要專業的基因諮詢。隨著基因檢測需求的增加，對提供此類服務的專業人員的需求也會相應增加。
        </p>
        <p><strong>展望未來</strong>
        </p>
        <p>
          隨著我們展望未來，基因檢測將在我們的生活中髮揮越來越重要的作用。測序成本的下降和技術的進步正鋪平道路，使得基因檢測在未來變得更加易得和有益。然而，在前進的衕時，我們必鬚確保能夠應對隨之而來的倫理複雜性、安全隱患和解讀挑戰。
        </p>
        <p>
          便宜且全麵的基因檢測的到來可能徹底改變從箇性化醫療到祖源追遡等領域。在醫療領域，基因檢測的普及可能會導緻遺傳病的早期髮現與預防、定製化治療和整體健康成果的改善。此外，瞭解我們遺傳的易感性可以鼓勵我們採取主動健康行爲和生活方式的調整。
        </p>
        <p>
          與此衕時，基因檢測的普及可以增強我們對人類歷史和箇人祖源的理解。這將使我們更加互聯互通，併體現我們共衕的遺傳遺産。
        </p>
        <p>
          然而，通曏這一未來的道路依然充滿挑戰。確保數據隱私和安全至關重要。基因數據的箇人性質要求採取嚴格的保護措施，防止其濫用。透明的數據使用和賦予用戶對其基因信息的控製權是朝著正確方曏邁齣的重要步驟。
        </p>
        <p>
          倫理問題是另一箇重要議題。使用基因信息造福人類與可能齣現的基因歧視或汙名化之間有一條微妙的界限。政策製定者和相關方必鬚確保我們的基因未來是公正、尊重併充滿正義的。
        </p>
        <p>
          最後，隨著基因檢測變得越來越普及，我們必鬚解決專業基因諮詢的需求。基因檢測結果的解讀併非總是直觀的，誤解可能導緻不必要的焦慮或錯誤的健康決策。增加基因諮詢師的可用性，併將基因諮詢納入基因檢測的過程，可以幫助箇人正確理解自己的結果。
        </p>
        <p>
          基因檢測的未來充滿潛力。當我們走曏這箇未來時，我們有機會將其塑造爲一箇充分利用基因信息的未來，衕時堅持倫理標準、保護隱私併確保準確解讀。我們現在的決策將決定我們如何航行在這一基因前沿，誰將從其中受益。
        </p>
        <p>
          基因檢測的前景廣闊，隨著我們謹慎應對未來的挑戰，我們正處於人類理解和健康的新紀元的前沿。隨著我們繼續解開基因代碼的複雜麵紗，我們不僅在解碼生命的構建塊，更在塑造人類的未來。
        </p>
        <p> 
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            <ol class="wp-block-list" start="1" style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;"> 
              <li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Wikipedia. (2022). 23andMe. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.OsMGPvmZh9CVZOXxGx4930AS1KrWWs07mYrBUcSsh0Y" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://en.wikipedia.org/wiki/23andMe</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.OsMGPvmZh9CVZOXxGx4930AS1KrWWs07mYrBUcSsh0Y" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">1</a></span></span>&nbsp;.</li>
      
              <li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Data Mining DNA. (2023). Who Has The Largest DNA Database? Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy5kYXRhbWluaW5nZG5hLmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.03RAmdcTG5xBBnivEjR-SVDG5KykBn1ppI5fAlk5bu0" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://www.dataminingdna.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy5kYXRhbWluaW5nZG5hLmNvbS93aG8taGFzLXRoZS1sYXJnZXN0LWRuYS1kYXRhYmFzZS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.xKmZH7QOwAsLmV566kw8xn7KKF7dshHtrjcBIE2sFMY" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">2</a></span></span>&nbsp;.</li>
      
              <li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Technology Review. (2019). More than 26 million people have taken an at-home ancestry test. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy50ZWNobm9sb2d5cmV2aWV3LmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.NzcMOiUbdxV-orFBkrB5hrsAazgNkjM5kIXkyg58SyI" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://www.technologyreview.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.H9RgDT-X1Aj9cEsj9DmRRRykmWfCZLcyWlhhZnDhBTM" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">3</a></span></span>&nbsp;.</li>
      
              <li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Know Your DNA. (2023). DNA Testing: Market Trends, Demographics, and Consumer Opinion. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL2tub3d5b3VyZG5hLmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.HmBZVtguscd0rdhvnZO4OH6X_KVabyXcygVtkU-V_7c" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://knowyourdna.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.K_fcErM_yG_hamqWo3Bdj_UoJF8edBF6yQ6D4Gxbzjc" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">4</a></span></span>&nbsp;.</li>
    </ol>
    <div class="post-tags"></div>
  </div>
</p>]]></description>
      
      <link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=50&amp;l=tw</link>
      <category>The Business Value of PGS</category>
      <pubDate>2025-02-11 03:19:00 +0800</pubDate>
    </item>
  
    <item>
      
      <title>瞭解消費級直銷基因檢測</title>
      <description><![CDATA[  <p><strong>初學者指南：消費級基因檢測——瞭解其工作原理、可揭示的信息以及如何解讀結果</strong></p>
<p>直銷基因檢測（DTC）是一種基因檢測類型，允許箇人在線或通過郵件訂購併接收基因檢測套件。這些套件通常包括一箇唾液或口腔拭子採集套件，消費者可以使用牠來收集自己的DNA樣本。樣本隨後寄迴公司進行分析，結果通過在線門戶或應用程序提供給消費者。</p>
<p>近年來，直銷基因檢測變得越來越流行，許多公司提供各種檢測選項。一些DTC基因檢測公司專註於祖源和傢譜，而其他公司則提供與健康相關的信息，如某些疾病的風險或藥物代謝情況。</p>
<p><strong>直銷基因檢測的工作原理</strong></p>
<p>DTC基因檢測的過程通常很簡單。首先，您需要選擇一箇公司和一箇檢測套件。市麵上有許多DTC基因檢測公司，選擇一箇信譽良好的公司非常重要。在選擇公司時，您應該尋找穫得臨床實驗室改進法案（CLIA）或美國病理學傢協會（CAP）認證的公司，因爲這些組織確保實驗室符閤一定的質量和準確性標準。</p>
<p>選擇好公司和檢測套件後，您需要訂購套件併按照説明收集DNA樣本。這通常包括提供唾液樣本或擦拭口腔內側的腮部。然後，您需要將樣本寄迴公司，併使用隨附的預付郵資包裝。</p>
<p>公司收到樣本後，他們將開始分析您的DNA。這箇過程通常需要幾週時間，結果會通過在線門戶或應用程序提供給您。</p>
<p><strong>DTC基因檢測能揭示的信息</strong></p>
<p>通過DTC基因檢測穫得的具體信息因公司和檢測套件的不衕而有所變化。以下是一些常見的信息類型：</p>
<ol>
  
          <li>
    <p><strong>祖源和傢譜</strong>：許多DTC基因檢測公司提供可以幫助您瞭解祖源和傢族歷史的檢測服務。這可能包括有關您的民族背景和祖先遷徙模式的信息。</p>
  </li>
  
        <li>
    <p><strong>某些疾病的風險</strong>：一些DTC基因檢測公司提供可以提供有關您患某些健康狀況風險的信息，例如阿爾茨海默病、帕金森病或某些類型的癌癥。需要註意的是，基因檢測隻能提供您患某一特定病癥的風險信息，而不能保證您一定會或不會得此病。</p>
  </li>
  
      <li>
    <p><strong>藥物代謝</strong>：一些DTC基因檢測公司提供可以幫助您瞭解身體如何代謝某些藥物的檢測。這對於服用多種藥物或曾經因某些藥物齣現副作用的人來説特彆有用。</p>
  </li>
  
    <li>
    <p><strong>攜帶者狀態</strong>：一些DTC基因檢測公司提供檢測，能夠告訴您是否是某些遺傳性疾病的攜帶者。這意味著您可能攜帶某種基因突變，盡管您自己併沒有這種疾病，但牠可能會傳遞給您的子女。</p>
  </li>
</ol>
<p><strong>解讀DTC基因檢測結果</strong></p>
<p>解讀DTC基因檢測結果可能會比較複雜，理解這一點很重要：基因檢測隻是您整體健康狀況的一箇組成部分。如果您對結果有任何問題或疑慮，最好諮詢醫療專業人員或基因顧問。</p>
<p>衕樣需要註意的是，DTC基因檢測併不能替代醫學檢測或建議。如果您對自己的健康狀況感到擔憂，重要的是諮詢醫療專業人員，併討論進一步檢測或治療的選項。</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=53&amp;l=tw</link>
      <category>關於遺傳檢測 More about Genetic Testing</category>
      <pubDate>2025-02-09 03:33:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>揭示基因檢測的衆多好處：從醫療洞察到祖源髮現</title>
      <description><![CDATA[  <p>近年來，基因檢測取得瞭長足的進展，爲箇體提供瞭更多瞭解自己基因的機會，以及基因如何影響健康和祖源的相關信息。本文將探討基因檢測的不衕用途及其可能帶來的好處。</p>
<p>首先，讓我們討論基因檢測的醫療用途。這種類型的檢測可以用來識彆可能增加箇體患上某些遺傳性疾病風險的基因變異。這些遺傳性疾病可以從遺傳性疾病，如囊性纖維化或鐮形細胞貧血，到更常見的疾病，如醣尿病或心髒病等。</p>
<p>基因檢測在醫療領域的主要好處之一是能夠及早識彆這些基因變異，從而幫助箇體採取預防措施，降低髮展該病的風險。例如，如果箇體擁有增加患乳腺癌風險的基因變異，他們可能會選擇定期篩查或改變生活方式，以降低風險。</p>
<p>除瞭幫助箇體做齣有關健康的知情決策外，基因檢測在醫療領域對傢庭也非常有益。例如，如果一對夫婦計劃要孩子，而其中一方擁有增加將某種遺傳病傳遞給後代的基因變異，基因檢測可以幫助他們理解選擇，併做齣關於生育的決策。</p>
<p><strong>基因檢測在祖源髮現中的應用</strong></p>
<p>另一種基因檢測的應用是祖源髮現。隨著消費型基因檢測套件的普及，箇體現在可以瞭解更多關於自己的祖源信息以及祖先的來歷。這對許多人來説是一次旣有趣又有意義的體驗，因爲牠使他們能夠與自己的遺産建立聯繫，深入瞭解傢族歷史。</p>
<p>基因檢測在祖源髮現中的主要好處之一是能夠填補箇體傢族歷史中的空白。例如，如果某箇箇體一直對自己的祖源感到好奇，但沒有很多線索，基因檢測可以幫助提供答案，讓他們更好地理解自己的祖源。</p>
<p>除瞭幫助箇體瞭解更多關於自己祖源的信息外，基因檢測在祖源髮現方麵對那些試圖重新聯繫失聯親鏚或識彆未知傢庭成員的傢庭也具有重要作用。例如，如果某箇箇體有一箇失聯的養兄妹或堂錶親，基因檢測可以幫助他們找到併重新聯繫上這箇人。</p>
<p><strong>基因檢測的多重好處</strong></p>
<p>基因檢測有很多潛在的好處，旣可以用於醫療目的，也可以用於祖源髮現。除瞭幫助箇體做齣有關健康和祖源的知情決策外，基因檢測還可以成爲傢庭重新聯繫失聯親鏚或瞭解傢族歷史的強大工具。</p>
<p>總體來説，基因檢測是一箇迅速髮展的領域，提供瞭讓箇體瞭解自己基因及其可能對健康和祖源産生影響的機會。無論是希望瞭解自己遺傳病風險的箇體，還是想要深入瞭解自己祖源的人，基因檢測都能提供寶貴的洞察，幫助做齣有關健康和傢庭的知情決策。</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=51&amp;l=tw</link>
      <category>關於遺傳檢測 More about Genetic Testing</category>
      <pubDate>2025-02-09 03:20:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>探索歐美頂尖基因檢測公司：全麵指南</title>
      <description><![CDATA[  <p>近年來，基因檢測越來越受到歡迎，成爲瞭解箇人祖源、識彆潛在健康風險以及做齣明智醫療決策的方式。市場上有許多基因檢測公司，每傢公司都提供各種服務和檢測選項。本文將概述一些最著名的基因檢測公司及其提供的服務。</p>
<p><strong>23andMe</strong><br />
    23andMe 可能是最著名的基因檢測公司之一。成立於2006年，該公司提供多種檢測選項，包括祖源檢測和健康風險評估。23andMe 的一箇獨特之處在於他們還提供攜帶者檢測，幫助箇人瞭解自己是否有將某些遺傳疾病傳給後代的風險。除瞭提供檢測結果，23andMe 還提供箇性化的基因報告和用於追蹤與解讀基因數據的工具。</p>
<p><strong>AncestryDNA</strong><br />
  AncestryDNA 是另一傢受歡迎的基因檢測公司，專註於祖源檢測。該公司成立於2012年，併迅速成爲全球最大的DNA祖源檢測服務提供商之一。AncestryDNA 提供多種檢測選項，包括祖源檢測、傢譜研究工具和DNA親屬匹配。除瞭提供檢測結果，該公司還提供教育資源和歷史記録數據庫，供傢譜研究使用。</p>
<p><strong>MyHeritage</strong><br />
  MyHeritage 是另一傢專註於祖源檢測的基因檢測公司。除瞭提供DNA檢測外，該公司還提供傢譜研究工具，併可訪問龐大的歷史記録數據庫。MyHeritage 還提供一箇名爲“種族估祘”的功能，根據箇體的DNA分析其祖源情況。</p>
<p><strong>Helix</strong><br />
  Helix 是一傢與其他公司閤作的基因檢測公司，提供多種檢測選項，包括祖源檢測、健康風險評估和攜帶者檢測。Helix 的獨特之處在於其“DNA應用商店”，允許用戶購買來自多箇閤作夥伴的基因數據洞察。</p>
<p><strong>Color Genomics</strong><br />
  Color Genomics 是一傢專註於健康風險評估的基因檢測公司。該公司提供多種檢測選項，包括全麵的基因健康風險評估和某些遺傳疾病的攜帶者檢測。Color Genomics 還提供箇性化的基因報告和基因顧問服務。</p>
<p><strong>基因檢測的局限性</strong><br />
  需要註意的是，盡管基因檢測可以提供關於祖源和潛在健康風險的寶貴信息，但牠併不能替代傳統的醫療護理。在根據基因檢測結果做齣任何決策之前，始終建議諮詢醫療專業人員。</p>
<p>隨著基因檢測技術的不斷進步和普及，未來我們可能會看到更多人齣於各種目的選擇進行基因檢測。未來，基因檢測有可能成爲常規醫療的一部分，箇人可以在定期體檢時接受基因風險評估。這有助於及早髮現潛在的健康問題，從而實現早期榦預，甚至預防某些疾病。</p>
<p><strong>箇性化醫療與基因檢測</strong><br />
  箇性化醫療是21世紀醫學的一大進展。這種方法旨在根據箇體的基因構成定製醫療治療方案。隨著箇性化醫療的普及，基因檢測的需求可能會激增。</p>
<p><strong>挑戰與考量</strong><br />
  盡管這些因素預示着基因檢測的未來充滿希望，但也必鬚考慮與這一增長相關的挑戰和倫理問題。</p>
<ol>
  
  <li>
    <p><strong>隱私和數據安全</strong>：隨著越來越多的人進行基因檢測，如何處理這些高度箇人化的數據變得癒髮重要。確保數據隱私和安全將是基因檢測公司麵臨的重大挑戰，尤其是在平衡商業需求與客戶權利和期望之間。</p>
  </li>
  
<li>
    <p><strong>倫理問題</strong>：基因檢測的倫理問題始終是討論的焦點。關於如何使用這些信息、誰應當訪問這些信息以及如何防止基因歧視的問題仍然在辯論中。</p>
  </li>
  
<li>
    <p><strong>解讀與諮詢</strong>：基因檢測結果的解讀較爲複雜，通常需要專業的基因諮詢。隨著基因檢測需求的增加，專業人員的需求也將隨之增長。</p>
  </li>
</ol>
<p><strong>未來展望</strong><br />
展望未來，基因檢測將在我們生活中扮演越來越重要的角色。隨著測序成本的下降和技術的進步，基因檢測的可穫取性和信息量將進一步增加。然而，隨著技術進步的衕時，我們也必鬚確保在倫理複雜性、安全性和解讀問題方麵的挑戰得到妥善處理。</p>
<p><strong>結論</strong><br />
基因檢測的前景廣闊，具有衆多潛在的應用和好處。雖然存在挑戰和倫理考量，但深入瞭解我們的基因將有可能革新醫療併改善全球人們的生活。在選擇基因檢測公司時，進行充分的研究併考慮公司提供的檢測選項、信譽以及解讀和理解測試結果的資源至關重要。</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=49&amp;l=tw</link>
      <category>關於遺傳檢測 More about Genetic Testing</category>
      <pubDate>2025-02-09 03:17:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>基因檢測的未來：可穫得性、進展與影響</title>
      <description><![CDATA[  <p>隨著我們邁曏21世紀，科學和技術不斷塑造我們對世界，尤其是對自身的理解。基因檢測是一箇迅速髮展併髮生轉型的領域。隨著測序成本的下降和全基因組測序技術的進步，基因檢測的格局將髮生深刻變化，且其可穫取性將大大提高，惠及更廣泛的人群。</p>
<p><strong>基因檢測的現狀</strong></p>
<p>爲瞭瞭解這一領域的未來髮展，首先需要瞭解當前的現狀。根據最新數據，已有數百萬人在美國使用過基因檢測服務。像23andMe、Ancestry.com和MyHeritage等公司分彆已經對超過500萬、2200萬和500萬箇人進行瞭基因分型，相關數據來自維基百科和DNA數據挖掘1 2 。</p>
<p>全球範圍內，基因檢測的普及程度更廣。技術評論預計，全球已有約3850萬到5000萬人進行瞭傢用DNA檢測，標誌著這一趨勢的全球化3 4 。</p>
<p><strong>展望未來</strong></p>
<p>展望未來，基因檢測將在我們的生活中扮演越來越重要的角色。隨著測序成本的下降和技術的進步，如《瞭解你的DNA》報告所述，未來基因檢測將變得更加易得且信息更爲豐富4 。</p>
<p>《DNA數據挖掘》強調，便宜且全麵的基因檢測將可能徹底改變從箇性化醫療到祖源追遡等各箇領域2 。</p>
<p>然而，通曏這一未來的道路充滿挑戰。確保數據隱私和安全至關重要。基因數據的箇人性質和敏感性要求採取嚴格的措施來防止其被濫用。關於數據使用的透明性以及用戶控製其基因信息的權利是朝著正確方曏邁齣的重要步驟，正如《技術評論》所討論的那樣3 。</p>
<p>基因檢測的未來充滿潛力。當我們邁曏這一未來時，我們有機會將其塑造爲一箇在利用基因信息的衕時，遵守倫理標準、保護隱私併確保準確解讀的未來。我們現在所做的決定將決定我們如何走曏這一基因前沿，併決定誰能從中受益，正如《瞭解你的DNA》所強調的那樣4 。</p>
<p><strong>可負擔性</strong>：自2003年人類基因組計劃完成以來，基因測序成本持續下降。這箇被稱爲“DNA測序成本麴線”的趨勢，已將2001年完成一次人類基因組測序的成本從1億美元降至2020年的約1000美元。隨著這一趨勢的繼續，基因檢測變得更加經濟實惠，更多人可以穫得這種檢測。</p>
<p><strong>技術進步</strong>：與測序成本下降衕時，技術的進步使得測序過程變得更加全麵。全基因組測序（WGS）就是一箇例子，牠能夠完整讀取箇體的基因組，這能提供關於箇體基因的詳細信息，這對理解健康風險、祖源以及其他遺傳特徵至關重要。</p>
<p><strong>公衆意識與需求的增加</strong>：隨著公衆對基因學的理解不斷加深，基因檢測服務的需求也隨之增加。這些服務可以滿足從好奇自己祖源到主動管理健康等多種需求。</p>
<p><strong>精準醫療</strong>：21世紀的一箇重大醫療髮展是精準醫療的興起。這種方法旨在根據箇體獨特的基因構成量身定製醫療治療方案。隨著精準醫療的普及，基因檢測的需求可能會激增。</p>
<p><strong>挑戰與考慮因素</strong></p>
<p>盡管這些因素預示着基因檢測的未來前景光明，但我們也必鬚考慮到隨著這一領域的增長而來的挑戰和倫理問題。</p>
<p><strong>隱私與數據安全</strong>：隨著越來越多的人進行基因檢測，關於這些高度箇人化的數據將如何被處理的問題變得越來越重要。確保數據隱私和安全將成爲基因檢測公司的一項重大挑戰，他們需要在商業需求和客戶權利與期望之間找到平衡。</p>
<p><strong>倫理問題</strong>：倫理問題始終處於基因檢測的前沿。如何使用這些信息、誰應該擁有這些數據的訪問權、如何防止基因歧視等問題仍在討論之中。</p>
<p><strong>解讀與諮詢</strong>：基因檢測結果的解讀複雜，往往需要專業的基因諮詢。隨著基因檢測需求的增加，對提供此類服務的專業人員的需求也會相應增加。</p>
<p><strong>展望未來</strong></p>
<p>隨著我們展望未來，基因檢測將在我們的生活中髮揮越來越重要的作用。測序成本的下降和技術的進步正鋪平道路，使得基因檢測在未來變得更加易得和有益。然而，在前進的衕時，我們必鬚確保能夠應對隨之而來的倫理複雜性、安全隱患和解讀挑戰。</p>
<p>便宜且全麵的基因檢測的到來可能徹底改變從箇性化醫療到祖源追遡等領域。在醫療領域，基因檢測的普及可能會導緻遺傳病的早期髮現與預防、定製化治療和整體健康成果的改善。此外，瞭解我們遺傳的易感性可以鼓勵我們採取主動健康行爲和生活方式的調整。</p>
<p>與此衕時，基因檢測的普及可以增強我們對人類歷史和箇人祖源的理解。這將使我們更加互聯互通，併體現我們共衕的遺傳遺産。</p>
<p>然而，通曏這一未來的道路依然充滿挑戰。確保數據隱私和安全至關重要。基因數據的箇人性質要求採取嚴格的保護措施，防止其濫用。透明的數據使用和賦予用戶對其基因信息的控製權是朝著正確方曏邁齣的重要步驟。</p>
<p>倫理問題是另一箇重要議題。使用基因信息造福人類與可能齣現的基因歧視或汙名化之間有一條微妙的界限。政策製定者和相關方必鬚確保我們的基因未來是公正、尊重併充滿正義的。</p>
<p>最後，隨著基因檢測變得越來越普及，我們必鬚解決專業基因諮詢的需求。基因檢測結果的解讀併非總是直觀的，誤解可能導緻不必要的焦慮或錯誤的健康決策。增加基因諮詢師的可用性，併將基因諮詢納入基因檢測的過程，可以幫助箇人正確理解自己的結果。</p>
<p>基因檢測的未來充滿潛力。當我們走曏這箇未來時，我們有機會將其塑造爲一箇充分利用基因信息的未來，衕時堅持倫理標準、保護隱私併確保準確解讀。我們現在的決策將決定我們如何航行在這一基因前沿，誰將從其中受益。</p>
<p>基因檢測的前景廣闊，隨著我們謹慎應對未來的挑戰，我們正處於人類理解和健康的新紀元的前沿。隨著我們繼續解開基因代碼的複雜麵紗，我們不僅在解碼生命的構建塊，更在塑造人類的未來。</p>
<p>
  <div class="page-content" style="font-family:Quicksand, sans-serif;font-size:16px;text-wrap-mode:wrap;background-color:#FFFFFF;">
    <ol class="wp-block-list" start="1" style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">
      
<li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Wikipedia. (2022). 23andMe. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.OsMGPvmZh9CVZOXxGx4930AS1KrWWs07mYrBUcSsh0Y" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://en.wikipedia.org/wiki/23andMe</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.OsMGPvmZh9CVZOXxGx4930AS1KrWWs07mYrBUcSsh0Y" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">1</a></span></span>&nbsp;.</li>
      
<li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Data Mining DNA. (2023). Who Has The Largest DNA Database? Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy5kYXRhbWluaW5nZG5hLmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.03RAmdcTG5xBBnivEjR-SVDG5KykBn1ppI5fAlk5bu0" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://www.dataminingdna.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy5kYXRhbWluaW5nZG5hLmNvbS93aG8taGFzLXRoZS1sYXJnZXN0LWRuYS1kYXRhYmFzZS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.xKmZH7QOwAsLmV566kw8xn7KKF7dshHtrjcBIE2sFMY" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">2</a></span></span>&nbsp;.</li>
      
<li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Technology Review. (2019). More than 26 million people have taken an at-home ancestry test. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL3d3dy50ZWNobm9sb2d5cmV2aWV3LmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.NzcMOiUbdxV-orFBkrB5hrsAazgNkjM5kIXkyg58SyI" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://www.technologyreview.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.H9RgDT-X1Aj9cEsj9DmRRRykmWfCZLcyWlhhZnDhBTM" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">3</a></span></span>&nbsp;.</li>
      
<li style="margin-block:0px;border:0px;outline:0px;vertical-align:baseline;background:transparent;">Know Your DNA. (2023). DNA Testing: Market Trends, Demographics, and Consumer Opinion. Retrieved from&nbsp;<span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.eyJ1cmwiOiJodHRwczovL2tub3d5b3VyZG5hLmNvbS8_dXRtX3NvdXJjZT1jb3Zlcm15Z2VuZXRpY3MuYmVlaGlpdi5jb20mdXRtX21lZGl1bT1yZWZlcnJhbCZ1dG1fY2FtcGFpZ249dGhlLWZ1dHVyZS1vZi1nZW5ldGljLXRlc3RpbmctYWNjZXNzaWJpbGl0eS1hZHZhbmNlbWVudHMtYW5kLWltcGxpY2F0aW9ucyIsInBvc3RfaWQiOiIxZmJhNGUxNi04MzQxLTQ5OTktODQzZS0xZmFiNmUwN2YxNmMiLCJwdWJsaWNhdGlvbl9pZCI6ImEyYmU3ODlhLTE1MDctNDc0ZC05OWUyLTdlYzk3NTBlZTNjOCIsInZpc2l0X3Rva2VuIjoiMWU0MTNhNTEtY2IwYi00ZjRlLWI2ZDEtZjdmZDY1ZmVmMWUzIiwiaWF0IjoxNjg4MDA5ODgxLjk1NywiaXNzIjoib3JjaGlkIn0.HmBZVtguscd0rdhvnZO4OH6X_KVabyXcygVtkU-V_7c" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">https://knowyourdna.com/</a></span><span style="font-size:12px;line-height:0;position:relative;vertical-align:baseline;top:-0.5em;"><span style="font-weight:bolder;"><a href="https://flight.beehiiv.net/v2/clicks/eyJhbGciOiJIUzI1NiIsInR5cCI6IkpXVCJ9.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.K_fcErM_yG_hamqWo3Bdj_UoJF8edBF6yQ6D4Gxbzjc" target="_blank" rel="noreferrer noopener" style="text-decoration-line:underline;color:#CC3366;">4</a></span></span>&nbsp;.</li>
    </ol>
    <div class="post-tags"></div>
  </div>
</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=48&amp;l=tw</link>
      <category>關於遺傳檢測 More about Genetic Testing</category>
      <pubDate>2025-02-09 03:13:00 +0800</pubDate>
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    <item>
      
<title>解開DNA的奧秘：DNA檢測背後的科學</title>
      <description><![CDATA[  <p>生命的奧秘編碼在DNA的螺镟結構中，DNA是一種複雜的大分子，作爲所有生物體的藍圖。隨著我們深入進入21世紀，得益於DNA檢測技術的進步，我們對這一藍圖的理解已經呈指數級增長。本文將揭示DNA檢測的科學原理、流程及其能揭示的信息。</p>
<p><strong>DNA的基礎知識</strong></p>
<p>DNA，全稱脫氧核醣核痠，是一種由兩條鏈纏繞成雙螺镟形狀的分子。牠是遺傳信息的載體，是驅動生命複雜機製的軟件。每箇DNA分子由一繫列核苷痠組成，每箇核苷痠含有一箇磷痠基糰、一分子醣和四種氮鹼基之一：腺嘌呤（A）、胸腺嘧啶（T）、鳥嘌呤（G）或胞嘧啶（C）。這些鹼基的特定排列構成瞭每箇生物體獨特的遺傳代碼。</p>
<p><strong>DNA檢測的魔力</strong></p>
<p>DNA檢測，也稱爲DNA分析或基因分型，是一種分析樣本中遺傳物質的過程，以識彆其獨特的遺傳代碼。該技術涉及從樣本（如唾液）中提取DNA，對其進行擴增，然後分析DNA序列中的特定區域。通過這一過程穫得的信息可以揭示從祖源到健康狀況傾曏等各種信息。</p>
<p>目前使用的兩種主要DNA檢測方法是SNP基因分型和全基因組測序。</p>
<p><strong>SNP基因分型</strong></p>
<p>SNP基因分型是一種DNA檢測方法，檢查基因組中特定的位置，卽單核苷痠多態性（SNP）。SNP是DNA中箇體之間常見變異的位置。通過檢查這些SNPs，基因檢測公司可以提供關於祖先、特徵和健康傾曏的見解。像23andMe和AncestryDNA這樣的公司就使用這種類型的檢測。</p>
<p><strong>全基因組測序</strong></p>
<p>全基因組測序（WGS）則不衕，牠檢查箇體幾乎所有的DNA序列，包括非編碼區域。WGS可以提供更完整的箇體基因組圖譜，可能揭示一些SNP基因分型遺漏的稀有遺傳變異。然而，由於WGS生成的數據量巨大，解讀起來可能更複雜且成本更高。</p>
<p><strong>DNA檢測能告訴我們什麽？</strong></p>
<p><strong>祖源</strong>：DNA檢測徹底改變瞭傢譜學，使箇人能夠追遡其祖先的根源，併與全球的親鏚建立聯繫。通過將箇體的DNA與蔘考人群進行比較，公司可以估祘齣你祖先來自的地理區域。</p>
<p><strong>健康</strong>：某些遺傳變異與特定健康狀況的風險增加有關，例如乳腺癌或阿爾茨海默病。DNA檢測可以揭示你是否攜帶這些變異。然而，必鬚記住，攜帶與某種疾病相關的遺傳變異併不意味著你一定會患上該疾病——牠僅錶示你的風險高於平均水平。</p>
<p><strong>特徵</strong>：從你是否容易長雀斑到你對咖啡的耐受性，DNA檢測能夠揭示關於你身體特徵和生活方式因素的有趣信息。</p>
<p><strong>DNA檢測的未來</strong></p>
<p>DNA檢測的科學技術在不斷髮展。技術的進步和成本的降低意味著更多人能夠訪問他們的遺傳信息。隨著我們對遺傳學的理解不斷深入，從DNA中提取的信息將變得癒加有價值。</p>
<p>然而，在我們擁抱箇性化基因組學的新時代時，也必鬚註意DNA檢測的倫理和隱私問題。雖然這些測試可以提供有益的信息，但牠們也引髮瞭關於數據隱私和遺傳歧視的問題。</p>
<p>DNA檢測是一箇令人驚歎的工具，使我們能夠窺探自己的遺傳代碼，更好地瞭解自己。牠是連接複雜基因學世界和我們日常生活的橋樑。隨著每一項技術的進步，我們距離解鎖DNA中隱藏的更多秘密又近瞭一步，爲箇性化醫療和人類遺傳學的更深入理解鋪平瞭道路。</p>
<p>在繼續探索這一領域時，請記住，知識就是力量。我們越是理解DNA檢測背後的科學，就越能夠就我們的健康、祖源和未來做齣明智的決策。</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=47&amp;l=tw</link>
      <category>關於遺傳檢測 More about Genetic Testing</category>
      <pubDate>2025-02-09 03:07:00 +0800</pubDate>
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<title>Clinical Application of PRS</title>
      <description><![CDATA[  <p><strong>Polygenic Risk Scores (PRS)</strong> can be applied to <strong>clinical prediction</strong>, though there are both advantages and limitations to their use in a clinical setting.</p>
<h3>How PRS Can Be Applied to Clinical Prediction:</h3>
<ol>
  
<li>
    <p><strong>Risk Stratification</strong>:
PRS can be used to classify individuals into different risk categories for developing certain diseases (e.g., heart disease, diabetes, certain cancers). For example, if a patient’s PRS indicates a high genetic risk for cardiovascular disease, clinicians might recommend more frequent screenings or preventive interventions such as lifestyle changes, medication, or other monitoring strategies.</p>
  </li>
  
<li>
    <p><strong>Personalized Preventive Medicine</strong>:
By combining genetic risk (from PRS) with environmental and lifestyle data, clinicians can tailor preventive measures more effectively. For example, an individual with a high PRS for type 2 diabetes could receive personalized advice on diet, exercise, and weight management to mitigate their genetic risk.</p>
  </li>
  
<li>
    <p><strong>Early Detection</strong>:
PRS could assist in identifying individuals at a higher genetic risk for diseases that have no early symptoms, like certain cancers or neurodegenerative conditions (e.g., Alzheimer’s). This could lead to earlier interventions, surveillance programs, or the use of predictive tests (like imaging) at an earlier stage.</p>
  </li>
  
<li>
    <p><strong>Treatment Selection</strong>:
In some cases, PRS could guide clinicians in choosing the most appropriate treatments based on an individual’s genetic predisposition. For example, some medications may work better for individuals with certain genetic backgrounds, so understanding their PRS can help optimize therapy.</p>
  </li>
</ol>
<h3>Limitations in Clinical Application:</h3>
<ol>
  
<li>
    <p><strong>Polygenic Nature of Disease</strong>:
PRS is based on the cumulative effect of many small genetic variants. This makes it more challenging to predict diseases accurately because each variant contributes only a small part of the overall risk. Many common diseases also involve complex interactions between genetics and environmental factors, making it difficult to isolate the contribution of genes alone.</p>
  </li>
  
<li>
    <p><strong>Incomplete Prediction</strong>:
PRS does not guarantee the onset of a disease. It only estimates the <strong>relative risk</strong> compared to the general population. For example, someone with a high PRS for heart disease may still never develop the condition due to protective lifestyle choices, while someone with a low PRS might still develop the disease due to other risk factors like diet or stress.</p>
  </li>
  
<li>
    <p><strong>Genetic Data Interpretation</strong>:
The accuracy of PRS depends on the quality and scope of the genetic data used to create the score. While large population studies have been instrumental in identifying genetic variants, there may be important genetic factors that haven't yet been discovered. Also, PRS models are typically developed for populations of European descent, and their applicability to individuals from other ethnic backgrounds may be limited.</p>
  </li>
  
<li>
    <p><strong>Ethical and Psychological Concerns</strong>:
The use of genetic information, including PRS, can raise ethical issues, such as the potential for genetic discrimination (in employment or insurance), privacy concerns, and psychological impacts (e.g., anxiety or stress from knowing one is at high risk for a disease). In clinical practice, care must be taken in how the information is communicated to patients.</p>
  </li>
  
<li>
    <p><strong>Integration into Clinical Practice</strong>:
While research on PRS has progressed rapidly, its widespread adoption into clinical practice still faces challenges. Clinical guidelines for using PRS are still being developed, and healthcare providers need more training on how to interpret and apply these scores.</p>
  </li>
</ol>
<h3>Current and Future Applications:</h3>
<ul>
  
<li>
    <p><strong>Cardiovascular Diseases</strong>: PRS for cardiovascular risk is one of the most well-studied, and many studies suggest that it could be useful for identifying people at high risk for heart attacks or strokes. However, more evidence is needed on how to incorporate it into routine practice.</p>
  </li>
  
<li>
    <p><strong>Cancer</strong>: For some cancers (e.g., breast cancer), PRS is showing promise in helping to identify individuals at higher risk, although current clinical guidelines don’t yet recommend it as part of routine screening.</p>
  </li>
  
<li>
    <p><strong>Mental Health</strong>: PRS for psychiatric disorders (such as schizophrenia or depression) is an emerging area, but it is not yet ready for routine clinical use, as it faces significant challenges in terms of predictive power and how to integrate it with environmental and clinical factors.</p>
  </li>
</ul>
<p>In summary, while <strong>PRS holds significant potential for clinical prediction</strong> in areas like disease risk stratification, personalized medicine, and early detection, it’s not yet fully ready for widespread routine use in clinical practice. More research, improved accuracy, and better integration with other clinical data will be necessary for its full potential to be realized.</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=46&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2025-02-09 02:34:00 +0800</pubDate>
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    <item>
      
<title>What is PRS?</title>
      <description><![CDATA[  <p>A <strong>Polygenic Risk Score (PRS)</strong> is a numerical value that represents an individual's genetic predisposition to a certain trait or disease, based on the cumulative effect of multiple genetic variants. These variants, typically single nucleotide polymorphisms (SNPs), each contribute a small amount to the overall risk, and PRS aggregates their effects to give an overall prediction.</p>
<p>Here’s how it works:</p>
<ol>
  
<li>
    <p><strong>Genetic Variants</strong>: Researchers identify specific genetic variants that are associated with a particular trait or disease. These variants might not directly cause the condition, but rather increase or decrease the likelihood of its occurrence.</p>
  </li>
  
<li>
    <p><strong>Weighting of Variants</strong>: Each genetic variant is assigned a weight based on its statistical association with the trait. This weight is often derived from large-scale studies, such as genome-wide association studies (GWAS), which look for correlations between genetic markers and diseases or traits in large populations.</p>
  </li>
  
<li>
    <p><strong>Calculation of PRS</strong>: The individual’s genetic data is analyzed, and the PRS is calculated by summing the contributions (weighted values) of all relevant genetic variants. The higher the score, the greater the genetic predisposition to the trait or disease.</p>
  </li>
  
<li>
    <p><strong>Risk Prediction</strong>: PRS can help estimate an individual's relative risk for diseases like heart disease, diabetes, certain cancers, and mental health conditions. It doesn't guarantee that someone will develop the disease, but it can indicate whether they are at higher or lower risk compared to the general population.</p>
  </li>
</ol>
<h3>Use of PRS:</h3>
<ul>
  
<li><strong>Personalized Medicine</strong>: PRS can aid in predicting who might benefit from certain preventive interventions or treatments.</li>
  
<li><strong>Risk Stratification</strong>: It can be used by doctors to identify individuals who may need closer monitoring for particular conditions, even before symptoms appear.</li>
  
<li><strong>Genetic Counseling</strong>: For individuals with a family history of a disease, PRS can provide additional insight into their own genetic risk.</li>
</ul>
<p>While PRS is a useful tool for understanding genetic risk, it's important to note that genetics is only one piece of the puzzle. Environmental factors, lifestyle choices, and other non-genetic factors also play significant roles in disease development.</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=45&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2025-02-09 02:32:00 +0800</pubDate>
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    <item>
      
<title>How do your genetics influence your health risks?</title>
      <description><![CDATA[  <p>Your genetics play a significant role in determining your predisposition to various health conditions. Certain genetic variations (mutations or polymorphisms) can influence how your body responds to factors like diet, lifestyle, environment, and even medications. Here's a breakdown of how your genetic data can affect your health risks:</p>
<h3>1. <strong>Genetic Predisposition to Diseases:</strong></h3>
<p>Some genetic variations are linked to an increased risk of developing specific diseases, such as:</p>
<ul>
  
<li><strong>Cardiovascular diseases</strong> (e.g., heart disease, high cholesterol)</li>
  
<li><strong>Cancer</strong> (e.g., breast cancer linked to BRCA1/BRCA2 mutations)</li>
  
<li><strong>Neurodegenerative diseases</strong> (e.g., Alzheimer's, Parkinson’s)</li>
  
<li><strong>Metabolic disorders</strong> (e.g., diabetes, obesity)</li>
  
<li><strong>Autoimmune diseases</strong> (e.g., rheumatoid arthritis, lupus)</li>
</ul>
<p>These genetic factors don’t guarantee you’ll develop the condition, but they increase the likelihood based on the presence of certain risk genes.</p>
<h3>2. <strong>Carrier Status for Inherited Conditions:</strong></h3>
<p>Some genetic disorders are inherited in an autosomal recessive pattern, meaning you need two copies of a mutated gene (one from each parent) to develop the condition. For example:</p>
<ul>
  
<li><strong>Cystic fibrosis</strong></li>
  
<li><strong>Sickle cell anemia</strong></li>
  
<li><strong>Tay-Sachs disease</strong></li>
</ul>
<p>You may be a carrier of a condition without exhibiting symptoms, but you can still pass it on to your children if they inherit the gene.</p>
<h3>3. <strong>Pharmacogenomics (Drug Response):</strong></h3>
<p>Your genetics can also influence how your body processes and responds to medications. Some variations affect:</p>
<ul>
  
<li><strong>Drug metabolism</strong>: Some people metabolize drugs faster or slower, which can affect how well a medication works or how toxic it might be at standard dosages.</li>
  
<li><strong>Efficacy and side effects</strong>: Genetic factors can determine whether a medication will be effective or whether it could cause adverse side effects.</li>
</ul>
<h3>4. <strong>Genetic Factors and Environmental Interactions:</strong></h3>
<p>Your genes may not act alone—environmental factors such as diet, exercise, and exposure to toxins can interact with genetic predispositions to modify health risks. For example, someone with a genetic predisposition to high cholesterol might only develop heart disease if they also have an unhealthy diet or lifestyle.</p>
<h3>5. <strong>Polygenic Risk Scores:</strong></h3>
<p>In some cases, health risks are influenced by many small genetic variations, each contributing a little bit to your overall risk. These can be combined into a <strong>polygenic risk score</strong> (PRS) that provides an estimate of your genetic predisposition to a specific disease. PRS is becoming more widely used for diseases like heart disease, diabetes, and some cancers.</p>
<h3>6. <strong>Genetic Testing and Risk Assessment:</strong></h3>
<p>There are now genetic tests that can provide insights into your health risks. These tests analyze your DNA for known mutations and provide risk estimates for various conditions. The results can help with early detection, prevention, and lifestyle changes to reduce the impact of these risks.</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=44&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2025-02-09 02:25:00 +0800</pubDate>
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<title>G2H-CVD1.0 心血管疾病風險評估示例報告 sample report Simplified Chinese</title>
      <description><![CDATA[  <h1 style="font-size:34px;font-family:&quot;font-weight:500;line-height:1.2;color:#317EAC;text-wrap-mode:wrap;background-color:#FFFFFF;"></h1>
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<h1 style="font-size:34px;font-family:&quot;font-weight:500;color:#317EAC;">
<img src="https://gene2h.com/file.php?f=202502/f_6cff37436d3469b69e66d1e61cde0e59&t=png&o=&s=&v=1738730899" alt /><br /></h1>
<p style="color:#555555;font-family:&quot;font-size:14px;"><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=41&amp;l=tw</link>
      <category>The Benefits of PGS</category>
      <pubDate>2025-02-07 12:59:00 +0800</pubDate>
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<title>G2H-CVD1.0 mobile</title>
      <description><![CDATA[  
<meta charset="UTF-8" />
<meta name="viewport" content="width=device-width, initial-scale=1.0" />
<title>YouTube Video Embed</title>
<h1>Watch the YouTube Short</h1>
<iframe width="560" height="315" src="https://www.youtube.com/embed/mQ-UCI2JGIM" frameborder="0" allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>]]></description>
      
<link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=42&amp;l=tw</link>
      <category>More Videos</category>
      <pubDate>2025-02-07 12:59:00 +0800</pubDate>
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<title>G2H sample report</title>
      <description><![CDATA[  
<img src="https://gene2h.com/file.php?f=202307/f_e870af9c5e52e2afee2e099cd7c1efcd&t=jpg&o=&s=&v=1690458318" alt /><br />
]]></description>
      
<link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=43&amp;l=tw</link>
      <category>The Benefits of PGS</category>
      <pubDate>2025-02-05 13:01:29 +0800</pubDate>
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<title>G2H-CVD1.0 心血管疾病風險評估示例報告 sample report Simplified Chinese</title>
      <description><![CDATA[  <h1 style="font-size:34px;font-family:&quot;font-weight:500;line-height:1.2;color:#317EAC;text-wrap-mode:wrap;background-color:#FFFFFF;"></h1>
<h1 style="font-size:34px;font-family:&quot;font-weight:500;line-height:1.2;color:#317EAC;text-wrap-mode:wrap;background-color:#FFFFFF;"></h1>
<h1 style="font-size:34px;font-family:&quot;font-weight:500;color:#317EAC;"></h1>
<h1 style="font-size:34px;font-family:&quot;font-weight:500;color:#317EAC;">
<img src="https://gene2h.com/file.php?f=202502/f_6cff37436d3469b69e66d1e61cde0e59&t=png&o=&s=&v=1738730899" alt /><br /></h1>
<p style="color:#555555;font-family:&quot;font-size:14px;"><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=40&amp;l=tw</link>
      <category>示例報告Sample Report</category>
      <pubDate>2025-02-05 12:43:00 +0800</pubDate>
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<title>G2H-CVD1.0 心血管疾病風險評估示例報告 sample report Traditional Chinese </title>
      <description><![CDATA[  <h1 style="font-size:34px;font-family:&quot;font-weight:500;line-height:1.2;color:#317EAC;text-wrap-mode:wrap;background-color:#FFFFFF;">
<img src="https://gene2h.com/file.php?f=202502/f_e9e7db29e4b1f88700560814b538946d&t=png&o=&s=&v=1738731267" alt /><br /></h1>
<div style="color:#555555;font-family:&quot;font-size:14px;text-wrap-mode:wrap;background-color:#FFFFFF;text-align:center;">
  <p style="margin-bottom:10px;"><br /></p>
</div>
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=39&amp;l=tw</link>
      <category>示例報告Sample Report</category>
      <pubDate>2025-02-05 12:42:00 +0800</pubDate>
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    <item>
      
<title>G2H-CVD1.0 sample report English</title>
      <description><![CDATA[  <h1 style="font-size:34px;font-family:&quot;font-weight:500;line-height:1.2;color:#317EAC;text-wrap-mode:wrap;background-color:#FFFFFF;">
<img src="https://gene2h.com/file.php?f=202502/f_c2b03cedae013e90f4fc97587618c4ca&t=png&o=&s=&v=1738730899" alt /><br /></h1>
<p style="margin-bottom:10px;color:#555555;font-family:&quot;font-size:14px;text-wrap-mode:wrap;background-color:#FFFFFF;"><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=38&amp;l=tw</link>
      <category>産品信息 Product Info     </category>
      <pubDate>2025-02-05 12:40:00 +0800</pubDate>
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    <item>
      
<title>G2H-CVD1.0 mobile</title>
      <description><![CDATA[  
<meta charset="UTF-8" />
<meta name="viewport" content="width=device-width, initial-scale=1.0" />
<title>YouTube Video Embed</title>
<h1>Watch the YouTube Short</h1>
<iframe width="560" height="315" src="https://www.youtube.com/embed/mQ-UCI2JGIM" frameborder="0" allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=37&amp;l=tw</link>
      <category>産品信息 Product Info     </category>
      <pubDate>2025-02-05 12:34:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>G2H sample report view</title>
      <description><![CDATA[  <p>View the report here 點擊查看示例報告</p>
<p><a href="https://connecthkuhk-my.sharepoint.com/:b:/g/personal/lane_connect_hku_hk/EWmp7JX8O-lNvEgTUw4NGnAB2rVXaxpFEz0jyDsuNveLYQ?e=ttxyC6" target="_blank">https://connecthkuhk-my.sharepoint.com/:b:/g/personal/lane_connect_hku_hk/EWmp7JX8O-lNvEgTUw4NGnAB2rVXaxpFEz0jyDsuNveLYQ?e=ttxyC6</a></p>
<p><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=36&amp;l=tw</link>
      <category>36</category>
      <pubDate>2025-02-05 12:24:00 +0800</pubDate>
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    <item>
      
<title>我們的服務範圍和報價</title>
      <description><![CDATA[  <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span></span><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:18pt;font-family:宋體;">服務範圍和報價</span></b>
<b><span style="font-size:18pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:宋體;">介紹</span></b>
<b><span style="font-size:13.5pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Gene to Health Limited </span></b><span style="font-size:12pt;font-family:宋體;">很高興爲您量身定做我們全麵的服務範圍和報價，以支持您的研究實驗室的數據分析和組學研究需求。</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">利用我們在人類遺傳學和生物信息學分析方麵的專業知識，我們緻力於提供博士水平的、高質量的、經濟高效的解決方案，以助力您的研究取得成功。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span></span><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:宋體;">報價單</span></b>
<b><span style="font-size:13.5pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">所有基本價格均以港幣（</span></b>
<b><span style="font-size:12pt;font-family:&quot;">HKD</span></b>
<b><span style="font-size:12pt;font-family:宋體;">）爲單位，併會根據項目範圍和具體要求髮生變化。</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<table class="MsoTable15List4 ke-select-col" border="1" cellspacing="0" cellpadding="0" width="595" style="width:446.55pt;border-collapse:collapse;border:none;">
  <tbody>
    <tr>
      <td width="236" valign="top" style="border:1pt solid black;background:black;">
        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;color:white;">服務</span></b>
<b><span style="font-size:12pt;font-family:&quot;color:white;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid black;background:black;">
        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;color:white;">描述</span></b>
<b><span style="font-size:12pt;font-family:&quot;color:white;"></span></b></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid black;background:black;">
        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;color:white;">每箇項目的基本價格（港元）</span></b>
<b><span style="font-size:12pt;font-family:&quot;color:white;"></span></b></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">生物信息學服務</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">基於</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> GWAS </span></b>
<b><span style="font-size:12pt;font-family:宋體;">的統計分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">使用多種工具進行全麵的芯片遺傳數據分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">10,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">單細胞組學分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">詳細的單細胞基因組和轉録組學分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">20,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">3. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">多基因風險評分</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">（</span></b>
<b><span style="font-size:12pt;font-family:&quot;">PRS</span></b>
<b><span style="font-size:12pt;font-family:宋體;">）</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">開髮</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">PRS </span><span style="font-size:12pt;font-family:宋體;">訓練、建模和驗證</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">8,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">4. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">流行病學統計模型</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Cox</span><span style="font-size:12pt;font-family:宋體;">和其他統計模型的實現</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">5,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">5. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">監督式機器學習模型</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">基於生物醫學數據的</span><span style="font-size:12pt;font-family:&quot;">ML</span><span style="font-size:12pt;font-family:宋體;">模型的開髮和評估</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">3,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">6. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">下一代測序</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">（</span></b>
<b><span style="font-size:12pt;font-family:&quot;">NGS</span></b>
<b><span style="font-size:12pt;font-family:宋體;">）</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">全麵的</span><span style="font-size:12pt;font-family:&quot;">NGS</span><span style="font-size:12pt;font-family:宋體;">數據分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">20,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">7. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">長讀長測序分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">長讀長測序數據分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">25,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">8. GWAS </span></b>
<b><span style="font-size:12pt;font-family:宋體;">後分析</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">全麵的</span><span style="font-size:12pt;font-family:&quot;">GWAS</span><span style="font-size:12pt;font-family:宋體;">後分析服務</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">15,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">9. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">孟德爾隨機化</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">用於推斷因果關繫的孟德爾隨機化分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">8,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">10. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">巨集基因組數據分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">宏基因組數據的分類和功能分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">15,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">11. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">多組學數據集成</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">整閤各種組學數據進行全麵分析</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">10,000</span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">一般服務</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. AWS </span></b>
<b><span style="font-size:12pt;font-family:宋體;">雲服務設置</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">基於雲的數據管理和報告繫統的開髮</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">30,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">英文稿件編輯和潤色</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">科學手稿的專業編輯服務</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">3,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">每篇手稿</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">3. R </span></b>
<b><span style="font-size:12pt;font-family:宋體;">和</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> Python </span></b>
<b><span style="font-size:12pt;font-family:宋體;">數據可視化和圖形閤成</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">創建自定義數據可視化</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">2,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">每箇圖</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加服務</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">a. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">數據可視化儀錶闆</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">互動式儀錶闆的開髮</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">8,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">b. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">生物信息學諮詢</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">戰略規劃和定製渠道開髮</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">6,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">每節課</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">c. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">技術支持和培訓</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">用戶培訓和持續的技術支持</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">5,000 </span><span style="font-size:12pt;font-family:宋體;">美元</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:宋體;">每月</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
  </tbody>
</table>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b>
<i><span style="font-size:12pt;font-family:宋體;">估計總成本：</span></i></b>
<b>
<i><span style="font-size:12pt;font-family:&quot;"> </span></i></b>
<i><span style="font-size:12pt;font-family:宋體;">因所選服務而異</span></i><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b>
<i><span style="font-size:12pt;font-family:宋體;">特彆套餐優惠：</span></i></b><span style="font-size:12pt;font-family:宋體;">對於選擇多種（</span><span style="font-size:12pt;font-family:&quot;">&gt;3</span><span style="font-size:12pt;font-family:宋體;">）服務的客戶，可享受</span><span style="font-size:12pt;font-family:&quot;"> 
<b><span>10%</span></b></span>
<b><span style="font-size:12pt;font-family:宋體;">的摺扣</span></b><span style="font-size:12pt;font-family:宋體;">。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span></span><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:宋體;">條款與細則</span></b>
<b><span style="font-size:13.5pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">一.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">付款條件：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">協議時預付</span><span style="font-size:12pt;font-family:&quot;">30%</span><span style="font-size:12pt;font-family:宋體;">，項目完成後</span><span style="font-size:12pt;font-family:&quot;">70%</span><span style="font-size:12pt;font-family:宋體;">。</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">或者通過談判的裡程碑。</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">所有付款應在髮票日期後</span><span style="font-size:12pt;font-family:&quot;"> 30 </span><span style="font-size:12pt;font-family:宋體;">天內結清。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">二.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">交貨時間：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">取決於項目範圍</span><span style="font-size:12pt;font-family:&quot;">; </span><span style="font-size:12pt;font-family:宋體;">預計</span><span style="font-size:12pt;font-family:&quot;">2-12</span><span style="font-size:12pt;font-family:宋體;">週。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">三.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">修訂：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">每箇可交付結果最多包括兩輪主要修訂和五輪次要修訂。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">四.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">保密性：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">所有客戶數據都將嚴格保密。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">五.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">有效期：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">報價自簽發之日起</span><span style="font-size:12pt;font-family:&quot;"> 30 </span><span style="font-size:12pt;font-family:宋體;">天內有效。</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;text-indent:-18pt;"><span style="font-size:12pt;font-family:&quot;">六.<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp; </span></span>
<b><span style="font-size:12pt;font-family:宋體;">可交付性：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">所有分析的數據、軟件輸齣、渠道指令和可交付結果（例如數字、錶格、訓練模型、蔘數）都將返迴給客戶。</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">生成的腳本的可用性是可以協商的，具體取決於閤衕範圍、客戶需求和關鍵知識産權的蔘與。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span></span><span style="font-size:12pt;font-family:&quot;"></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:16pt;font-family:宋體;">服務範圍</span></b>
<b><span style="font-size:16pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:宋體;">生物信息學服務</span></b>
<b><span style="font-size:13.5pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">基於</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> GWAS </span></b>
<b><span style="font-size:12pt;font-family:宋體;">的統計分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">描述：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">遺傳數據的綜閤全基因組關聯分析</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">（</span><span style="font-size:12pt;font-family:&quot;">GWAS</span><span style="font-size:12pt;font-family:宋體;">），以確定遺傳變異與各種錶型性狀之間的關聯。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">工具和軟件</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">主要：</span></b><span style="font-size:12pt;font-family:&quot;"> PLINK</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">REGENIE</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">GCTA</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">GATK</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">LDSC</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">FUMA</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">BOLT-LMM</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">EIGENSOFT</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">SNPTEST</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">EMMAX</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">METAL</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">FINEMAP</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">渠道和流程：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">數據清理和品質控製：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">通過去除低質量的樣本和變體來確保數據完整性。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">種群分層：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">使用主成分分析</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">（</span><span style="font-size:12pt;font-family:&quot;">PCA</span><span style="font-size:12pt;font-family:宋體;">）</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">校正種群結構。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">全基因組關聯研究</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">（</span></b>
<b><span style="font-size:12pt;font-family:&quot;">GWAS</span></b>
<b><span style="font-size:12pt;font-family:宋體;">）：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">識別與特定性狀相關的重要遺傳變異。</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">遺傳力估計：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">計祘遺傳因素解釋的方差比例。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">插補：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">使用蔘考麵闆增強基因型數據完整性。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Meta </span></b>
<b><span style="font-size:12pt;font-family:宋體;">分析：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">結閤多項研究的結果以提高統計功效。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><a name="OLE_LINK1"></a><a name="OLE_LINK2"></a><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
<span style="font-size:medium;"></span><span style="font-size:medium;"></span><span style="font-size:medium;"></span>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">單細胞組學分析</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">描述：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">對單細胞基因組和轉録組數據進行詳細分析，以瞭解細胞異質性和複雜的生物過程。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">工具和軟件</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">主要：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">Partek Flow</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加功能：</span></b><span style="font-size:12pt;font-family:&quot;"> Seurat</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">Scanpy</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">CellRanger</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">Monocle</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">Drop-seq Tools</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">SingleR</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">渠道和流程：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">數據預處理：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">單細胞數據的質量控製、歸一化和縮放。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">聚類和降維：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">使用</span><span style="font-size:12pt;font-family:&quot;">PCA</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">t-SNE</span><span style="font-size:12pt;font-family:宋體;">或</span><span style="font-size:12pt;font-family:&quot;">UMAP</span><span style="font-size:12pt;font-family:宋體;">識別不衕的細胞群。</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">差異錶達分析：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">檢測跨簇錶達显著變化的基因。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">軌跡分析：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">推斷細胞髮育途徑和譜繫關繫。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">多模態數據的整閤：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">將單細胞</span><span style="font-size:12pt;font-family:&quot;"> RNA-seq </span><span style="font-size:12pt;font-family:宋體;">與其他數據類型（例如</span><span style="font-size:12pt;font-family:&quot;"> ATAC-seq</span><span style="font-size:12pt;font-family:宋體;">）相結閤。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">3. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">多基因風險評分</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">（</span></b>
<b><span style="font-size:12pt;font-family:&quot;">PRS</span></b>
<b><span style="font-size:12pt;font-family:宋體;">）</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">訓練、建模和測試</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">描述：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">開髮和驗證多基因風險評分，以根據遺傳數據預測箇體對各種健康狀況的易感性。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">工具和軟件</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">主要：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">PRSice</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">LDpred</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">PRS-CS</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加：</span></b><span style="font-size:12pt;font-family:&quot;"> PLINK</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">LASSOSUM</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">SBayesR</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">渠道和流程：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">SNP </span></b>
<b><span style="font-size:12pt;font-family:宋體;">選擇：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">識彆風險評分的相關遺傳變異。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">加權：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">根據</span><span style="font-size:12pt;font-family:&quot;"> GWAS </span><span style="font-size:12pt;font-family:宋體;">結果為每個</span><span style="font-size:12pt;font-family:&quot;"> SNP </span><span style="font-size:12pt;font-family:宋體;">分配效應大小。</span><span style="font-size:12pt;font-family:&quot;"></span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">分數計祘：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">聚閤加權</span><span style="font-size:12pt;font-family:&quot;"> SNP </span><span style="font-size:12pt;font-family:宋體;">以計祘單個</span><span style="font-size:12pt;font-family:&quot;"> PRS</span><span style="font-size:12pt;font-family:宋體;">。</span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">驗證：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">在獨立排隊中測試</span><span style="font-size:12pt;font-family:&quot;"> PRS </span><span style="font-size:12pt;font-family:宋體;">的預測準確性。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">優化：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">優化模型以提高預測性能。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">4. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">流行病學統計模型</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">描述：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">應用統計模型研究人群中健康相關狀態和事件的分佈和決定因素。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">工具和軟件</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">主要：</span></b><span style="font-size:12pt;font-family:&quot;"> R</span><span style="font-size:12pt;font-family:宋體;">（例如生存包）</span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加：</span></b><span style="font-size:12pt;font-family:&quot;"> Python</span><span style="font-size:12pt;font-family:宋體;">（例如</span><span style="font-size:12pt;font-family:&quot;"> statsmodels</span><span style="font-size:12pt;font-family:宋體;">）</span><span style="font-size:12pt;font-family:&quot;"></span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">渠道和流程：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Cox </span></b>
<b><span style="font-size:12pt;font-family:宋體;">比例風險模型：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">評估變量對事件髮生時間結果的影響。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">邏輯迴歸：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">對二元結果進行建模。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">線性迴歸：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">分析連續性狀。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">混閤效應模型：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">處理分層或縱曏數據結構。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">生存分析：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">估計生存函數和風險比。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">5. </span></b>
<b><span style="font-size:12pt;font-family:宋體;">監督式機器學習模型</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">描述：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">實施機器學習技術來預測結果併識彆數據中的模式。</span><span style="font-size:12pt;font-family:&quot;"><span></span></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">工具和軟件</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b>
<b><span style="font-size:12pt;font-family:宋體;">：</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">主要：</span></b><span style="font-size:12pt;font-family:&quot;"> scikit-learn </span><span style="font-size:12pt;font-family:宋體;">（</span><span style="font-size:12pt;font-family:&quot;">Python</span><span style="font-size:12pt;font-family:宋體;">）、隨機森林、支援曏量機</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">（</span><span style="font-size:12pt;font-family:&quot;">SVM</span><span style="font-size:12pt;font-family:宋體;">）、神經網路</span><span style="font-size:12pt;font-family:&quot;"></span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">附加：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">提陞演祘法：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">XGBoost</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">LightGBM</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">AdaBoost</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">CatBoost</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">深度學習框架：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">PyTorch</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">集成方法：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">梯度提陞機</span><span style="font-size:12pt;font-family:&quot;"> </span><span style="font-size:12pt;font-family:宋體;">（</span><span style="font-size:12pt;font-family:&quot;">GBM</span><span style="font-size:12pt;font-family:宋體;">）、額外的樹、裝袋</span><span style="font-size:12pt;font-family:&quot;"></span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">迴歸模型：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:&quot;">ElasticNet</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">Lasso</span><span style="font-size:12pt;font-family:宋體;">、</span><span style="font-size:12pt;font-family:&quot;">Ridge </span><span style="font-size:12pt;font-family:宋體;">迴歸</span><span style="font-size:12pt;font-family:&quot;"></span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">其他演祘法：</span></b>
<b><span style="font-size:12pt;font-family:&quot;"> </span></b><span style="font-size:12pt;font-family:宋體;">樸素貝葉斯、決策樹</span><span style="font-size:12pt;font-family:&quot;"></span></li>
  </ul>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:宋體;">渠道和流程：</span></b><span st]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=35&amp;l=tw</link>
      <category>服務內容 All services </category>
      <pubDate>2025-02-05 12:14:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Gene to Health Limited Team Profile</title>
      <description><![CDATA[  <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><br /></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<img src="https://gene2h.com/file.php?f=202502/f_e42f1c487360a746906e3a8005a091af&t=png&o=&s=&v=1711232369" alt /></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Team Profile</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Company website: https://gene2h.com</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Under the guidance of 
<b>Prof. Pak Sham</b>, Gene to Health Limited was founded in October 2022 with 
<b>Dr. Chen Guolan</b> as the founding CEO and 
<b>Dr. Justin Tubbs</b> as confounder and former CTO. The company is currently undergoing a three-year incubation at the Hong Kong Science and Technology Parks Corporation (HKSTP). The company develops multi-omics prediction technology with polygenic risk scoring as the core, with the goal of predicting, early screening and auxiliary diagnosis of various common and complex diseases such as childhood autism, Alzheimer's, depression, type 2 diabetes, hypertension, coronary artery disease, etc., combined with the AI-assisted virtual genetic counseling platform.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>The laboratory's research focuses on the intersection of statistical genetics, machine learning, genomics, and bioinformatics. Dr. Chen's research focuses on the application of multiple regular regression and Bayesian models to genomic big data mining of disease cohorts to achieve fine mapping of pathogenic genes in complex diseases and analysis of genetic structure of phenotypic groups. Dr. Chen holds a bachelor's degree in biostatistics from the School of Life Sciences of Fudan University, and recently graduated from the Department of Psychiatry of the Faculty of Medicine of the University of Hong Kong in 2024 under the supervision of Professor Pak Sham, a world-renowned human geneticist (with more than 150,000 citations). The R&amp;D scientists in the team are proficient in IT development and data science skills such as R language, Python, html5, database, cloud computing, etc., and are good at handling high-dimensional data analysis and complex model construction. The entrepreneurial team has accumulated rich experience in bioinformatics, genomics, and multimodal data analysis, and is committed to promoting the interdisciplinary application of biotechnology and pharmaceutical innovation.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Gene to Health Limited is the first in Asia to develop a practical application of polygenic scoring technology based on millions of disease-related genetic variant data, which can predict more than 800 traits and diseases at an early stage, and is now developing from the positioning of health management products to the clinical direction. We provide ultra-early and full-coverage disease and phenotype prediction services through genetic testing combined with questionnaires, nutritional data, physical examinations and medical records, proteomics and metabolomics data, etc., so that people can obtain a variety of health management and medical benefits, and ultimately help early screening, auxiliary diagnosis and early intervention of diseases. The technologies used by the company include statistical modeling, machine learning, big data analysis, epidemiological analysis, bioinformatics, database development, and AI large language model development.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Introduction to our core products</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Our core product suite is an integrated intelligent genetic prediction technology platform called Gene-to-Health (G2H). Trained on genomic research data (open data) from millions of people, the platform is able to make predictions about various human traits and common diseases based on an individual's genetic data (DNA variation information). This genetic data is easily available from test kits sold by most direct-to-consumer genetic testing vendors (e.g., Microgenetics, 23 Rubik's Cube). G2H provides more than just disease risk analysis; Combined with the generative AI model, it actually acts as a virtual genetic counselor, analyzing and explaining the customer's genetic test report through question-and-answer interaction, and providing intelligent and personalized nutrition, prevention and intervention suggestions. 
<b>At present, our platform is used by enterprise users in the gene industry for product development and scientific research services.</b></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>The cost of genetic testing has rapidly decreased and is currently affordable (hundreds to thousands of RMB) for most people. However, the effectiveness and benefits of all currently commercially available test kits in terms of healthcare are relatively weak. Most consumers don't feel the benefits because even well-known providers such as 23AndMe, Ancestry, and Microgene have very limited information about their personal health information. In order to attract more customers, the G2H platform can help them provide comprehensive healthcare prediction and fertility consultation advice services, adding a very attractive selling point. We envision that in the near future, people will be able to understand their (and their children's) future risk of developing common diseases for a single test that will not only be lifelong, but will always be updated with the accumulation of big data and technological advancements.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>The G2H platform is designed to help users optimize their lifestyles, prevent and manage related diseases, and improve their overall health by using advanced genomics analysis, personalized nutrition solutions, and health management systems in the following four areas:</span></p>
<ol style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Risk assessment and management of common diseases:<br /></span></b><span>Based on genetic data, physical examination reports, and lifestyle information, the G2H platform conducts risk assessment of common chronic diseases such as cardiovascular diseases, diabetes, and hypertension, and provides personalized health intervention suggestions according to the specific risk level of users. Through regular monitoring and precise management, the platform effectively helps users reduce the risk of disease and improve their quality of life.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Diet and Nutrition Optimization:</span></b><span><br />The G2H platform provides users with personalized dietary recommendations through in-depth analysis of individual genomes combined with accurate nutritional data, optimizes nutritional intake, and prevents diet-related chronic diseases, such as obesity, diabetes, and hypertension. The platform can also provide scientific dietary adjustment suggestions and recommended nutritional supplement plans by combining the dietary behavior and nutrient intake information provided by users.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Skin health management:</span></b><span><br />By analyzing users' genetic data, the G2H platform is able to identify genetic variants associated with skin aging, sensitivities, and diseases such as eczema and psoriasis. Combined with accurate skin care suggestions and lifestyle adjustments, we provide users with skin health management solutions and skin care product recommendations to delay aging, improve skin condition, and prevent the occurrence of skin diseases.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Cancer risk prediction and intervention:</span></b><span><br />Using mutant gene detection and big data analysis, the G2H platform provides users with personalized cancer risk predictions, especially for cancer types that are closely related to genetic genes (such as breast cancer and colon cancer). The platform combines nutrition, exercise and lifestyle interventions to provide scientific prevention and early screening recommendations.</span></li>
</ol>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Through these specialized applications, the G2H platform provides users with a full range of health management support, helping everyone achieve a healthier and better life.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>In addition to G2H's platform, the company has built other R&amp;D pipelines:</span></p>
<p class="1" align="left" style="font-size:medium;margin-left:18pt;text-indent:-18pt;"><span>1)<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>An intelligent genomic breeding screening platform for agricultural breedin (genomics-for-breeding, G4B);</span></p>
<p class="1" align="left" style="font-size:medium;margin-left:18pt;text-indent:-18pt;"><span>2)<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>G2H-Pet and G4B-Pet for Pet (Cat and Dog) Disease Prediction and Breeding;</span></p>
<p class="1" align="left" style="font-size:medium;margin-left:18pt;text-indent:-18pt;"><span>3)<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Genome-based multi-omics prediction and diagnosis tools for degenerative diseases such as Alzheimer's and Parkinson's disease;</span></p>
<p class="1" align="left" style="font-size:medium;margin-left:18pt;text-indent:-18pt;"><span>4)<span style="font-size:7pt;line-height:normal;font-family:&quot;">&nbsp;&nbsp;&nbsp;&nbsp; </span></span><span>Genome-guided medication consultation tool for breast cancer patients.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>The above pipelines are all in the early stage of research and development or concept verification.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Company vision</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Represented by the UK Biobank and the All of US cohort, the "Population Genome Project" and "Large Cohort", which are characterized by the simultaneous acquisition of genomic (multi-omics)-phenotype data of large samples in the same population, are emerging in countries around the world. These cohorts often have sample sizes ranging from hundreds of thousands to millions of people. The health information contained in genetic big data is a valuable resource for every group of people and nations, and is an indispensable part of building population health, precision medicine and good preventive medicine. As the world's most populous country and a multi-ethnic country, China is also striving for the top, and various scientific research units are uniting to promote the construction and development of the Chinese population. The company's long-term vision is to lay the infrastructure for the construction of the large fleet of Chinese people, and to do a good job in the development and preparation of research design and tools, software and algorithms, operation management and systems.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Prospects for cooperation</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Our G2H platform can be specialized and tuned for the prediction and evaluation of specific directions and types of diseases, such as cardiovascular disease prediction. We have created a sample version that does not require genetic data, aiming to help users assess the risk of cardiovascular disease (including heart attack and stroke) in the next 10 years through advanced genomic analysis and a variety of authoritative risk assessment methods based on questionnaire data, providing a scientific basis for health management and medical interventions. Try our demo and get your own report in English or Chinese for free at<a href="https://g2h.lanechen.xyz"> https://g2h.lanechen.xyz</a></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>Because the G2H platform covers more than 800 phenotypes and diseases, there is a huge potential for collaboration with partners who specialize in different areas by collaborating on the development of specialized applications.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>We can further improve the adaptability and scalability of the G2H platform through modular design and flexible interfaces, enabling it to quickly integrate algorithms and data sources from different domains. For example, partners can combine their own datasets and algorithms to work with our platform to develop customized solutions for specific populations, specific diseases, or specific scenarios. This open cooperation model can not only quickly respond to market demand, but also promote multi-party resource sharing and technological innovation.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>In addition, the G2H platform has strong data privacy protection capabilities, and ensures the security and compliance of user data through advanced encryption technology and de-identification processing. This makes the platform more advantageous in the field of healthcare, and can provide reliable data processing and analysis support for medical institutions, scientific research teams and business partners.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>In the future, we will further expand the application scope of the G2H platform, such as developing more efficient and accurate assessment tools for metabolic diseases, psychiatric diseases, geriatric diseases, neurological diseases and tumor risk prediction.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>Looking forward to working with you!</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>If you are interested in further negotiation or more information, please contact us:</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; •&nbsp;&nbsp;&nbsp;&nbsp; Contact information of CEO Dr. Chen Guolan</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;text-indent:21pt;"><span>Email</span><span style="font-family:宋體;">：</span><span><a href="mailto:lanechenhku@gmail.com">lanechenhku@gmail.com</a>;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;text-indent:21pt;"><span>WeChat</span><span style="font-family:宋體;">：</span><span>lane13318032043;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;text-indent:21pt;"><span>WhatsApp: +852 46404365</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; •&nbsp;&nbsp;&nbsp;&nbsp; Company Email:support@gene2h.com</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; •&nbsp;&nbsp;&nbsp;&nbsp; Official Website:<a href="http://www.gene2h.com">www.gene2h.com</a></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;"><span>&nbsp;</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:Calibri, sans-serif;">
<b><span>&nbsp;</span></b></p>
<p><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=34&amp;l=tw</link>
      <category>公司信息 Company Info</category>
      <pubDate>2025-02-05 12:11:00 +0800</pubDate>
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<title>聯繫我們 Contact Us</title>
      <description><![CDATA[  
<img src="https://gene2h.com/file.php?f=202502/f_fd04a20a15a88cb1b66ca2a1ddfe454b&t=png&o=&s=&v=1711232369" alt />]]></description>
      
<link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=33&amp;l=tw</link>
      <category>Others</category>
      <pubDate>2025-02-05 12:08:00 +0800</pubDate>
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<title>Watch more about us at our YouTube channel</title>
      <description><![CDATA[  ]]></description>
      
<link>https://gene2h.comhttps://www.youtube.com/channel/UC3HdUPsupU-TSgSfodhwVrQ</link>
      <category>Media News</category>
      <pubDate>2025-02-05 11:28:00 +0800</pubDate>
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    <item>
      
<title>Try G2H-CVD1.0</title>
      <description><![CDATA[  <p><strong>Welcome to G2H-CVD1.0 - Predict Your 10-Year Cardiovascular Disease Risk</strong></p>
<p>At G2H, we believe in empowering individuals to take control of their heart health with cutting-edge tools. Our <strong>G2H-CVD1.0</strong> is a powerful risk prediction model designed to assess your 10-year risk of developing cardiovascular disease (CVD).</p>
<h3>How It Works:</h3>
<ol>
  
<li><strong>Simple Inputs:</strong> Enter your basic health information, such as age, sex, cholesterol levels, blood pressure, and lifestyle factors.</li>
  
<li><strong>Advanced Predictive Model:</strong> Using state-of-the-art algorithms, <strong>G2H-CVD1.0</strong> analyzes your data to generate a personalized risk assessment for cardiovascular disease over the next 10 years.</li>
  
<li><strong>Get Your Free Report:</strong> Once you complete the input, you will receive a <strong>detailed risk prediction report</strong> along with personalized recommendations to improve your heart health.</li>
</ol>
<h3>Why Use G2H-CVD1.0?</h3>
<ul>
  
<li><strong>Accurate Predictions:</strong> G2H-CVD1.0 uses scientifically validated models to give you a reliable prediction.</li>
  
<li><strong>Personalized Recommendations:</strong> Based on your results, you’ll get tailored suggestions to improve your health.</li>
  
<li><strong>Completely Free:</strong> No hidden costs or requirements, just input your details and get your risk report.</li>
</ul>
<h3>Start Your Risk Prediction Today:</h3>
<p>Click on the button below to get started with the <strong>G2H-CVD1.0</strong> prediction tool.</p>
<p><a rel="noopener" target="_new" href="https://g2h.lanechen.xyz"><strong>Try G2H-CVD1.0 Now</strong></a></p>
<p><br /></p>
<p>https://g2h.lanechen.xyz</p>
<hr />
<p><strong>Important Notes:</strong></p>
<ul>
  
<li>The prediction is based on available health data. For a full health assessment, please consult a healthcare professional.</li>
  
<li>This tool is designed to provide general insights. Individual risk factors may vary.</li>
</ul>]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=31&amp;l=tw</link>
      <category>31</category>
      <pubDate>2025-02-05 11:25:00 +0800</pubDate>
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<title>G2H Scope of Services and Quotation</title>
      <description><![CDATA[  <div class="MsoNormal" align="center" style="margin:0cm;text-align:center;font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">
<hr /></span></div>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:18pt;font-family:&quot;">Scope of Services and Quotation</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:&quot;">Introduction</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Gene to Health Limited</span></b><span style="font-size:12pt;font-family:&quot;"> is pleased to present our comprehensive 
<b>Scope of Services</b> and 
<b>Quotation</b> tailored to support your research laboratory's data analysis and omics research needs. Leveraging our expertise in advanced genetic and bioinformatics analyses, we are committed to delivering PhD-level, high-quality, cost-effective solutions to enhance your research capabilities.</span></p>
<div class="MsoNormal" align="center" style="margin:0cm;text-align:center;font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">
<hr /></span></div>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:&quot;">Quotation</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">All base prices are in Hong Kong Dollars (HKD) and are subject to uprise change based on project scope and specific requirements.</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<table class="MsoTable15List4" border="1" cellspacing="0" cellpadding="0" width="595" style="width:446.55pt;border-collapse:collapse;border:none;">
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        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;color:white;">Service</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid black;background:black;">
        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;color:white;">Description</span></b></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid black;background:black;">
        <p class="MsoNormal" align="center" style="text-align:center;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;color:white;">Base Price (HKD) Per Project</span></b></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Bioinformatic Services</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
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      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. GWAS-based Statistical Genetic Analysis</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Comprehensive array genetic data analysis using multiple tools</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$10,000</span></p>
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      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. Single-Cell Omics Analysis</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Detailed single-cell genomic and transcriptomic analysis</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$20,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
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<b><span style="font-size:12pt;font-family:&quot;">3. Polygenic Risk Score (PRS) Development</span></b></p>
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      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">PRS training, modeling, and validation</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$8,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">4. Epidemiological Statistical Models</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Implementation of Cox and other statistical models</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$5,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">5. Supervised Machine Learning Models</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Development and evaluation of ML models on biomedical data</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$3,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">6. Next Generation Sequencing (NGS) Analysis</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Comprehensive NGS data analysis</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$20,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">7. Long Read Sequencing Analysis</span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Analysis of long-read sequencing data</span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$25,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">8. Post-GWAS Analyses</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Comprehensive post-GWAS analysis services</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$15,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">9. Mendelian Randomization</span></b></p>
      </td>
      <td width="246" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Mendelian Randomization analysis to infer causal relationships</span></p>
      </td>
      <td width="113" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$8,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">10. Metagenomic Data Analysis</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Taxonomic and functional profiling of metagenomic data</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$15,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">11. Multi-Omics Data Integration</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Integrating various omics data for comprehensive analysis</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$10,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">General Services</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. AWS Cloud Services Setup</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Development of cloud-based data management and report systems</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$30,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. English Manuscript Editing and Polishing</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Professional editing services for scientific manuscripts</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$3,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">per manuscript</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">3. R and Python Data Visualization and Figure Composition</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Creation of custom data visualizations</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$2,000</span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">per figure</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional Services</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">a. Data Visualization Dashboards</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Development of interactive dashboards</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$8,000</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">b. Bioinformatics Consulting</span></b>
<b><span style="font-size:12pt;font-family:&quot;"></span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">Strategic planning and custom pipeline development</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$6,000</span><span style="font-size:12pt;font-family:&quot;"></span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">per session</span><span style="font-size:12pt;font-family:&quot;"></span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">c. Technical Support and Training</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">User training and ongoing technical support</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">$5,000</span></p>
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">per month</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;background:#CCCCCC;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
    <tr>
      <td width="236" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></b></p>
      </td>
      <td width="246" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
      <td width="113" valign="top" style="border:1pt solid #666666;">
        <p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
      </td>
    </tr>
  </tbody>
</table>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b>
<i><span style="font-size:12pt;font-family:&quot;">Total Estimated Cost:</span></i></b><span style="font-size:12pt;font-family:&quot;"> 
<i>Varies based on selected services</i></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b>
<i><span style="font-size:12pt;font-family:&quot;">Special Package Offer:</span></i></b><span style="font-size:12pt;font-family:&quot;"> For clients opting for multiple (&gt;3) services, a 
<b>10% discount</b> is applicable.</span></p>
<div class="MsoNormal" align="center" style="margin:0cm;text-align:center;font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">
<hr /></span></div>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:&quot;">Terms and Conditions</span></b></p>
<ol style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Payment Terms:</span></b><span style="font-size:12pt;font-family:&quot;"> 30% upfront upon agreement, 70% upon project completion. Or by milestones upon negotiations. All payments shall be settled within 30 days against invoice date.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Delivery Timeframe:</span></b><span style="font-size:12pt;font-family:&quot;"> Dependent on project scope; estimated between 2-12 weeks.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Revisions:</span></b><span style="font-size:12pt;font-family:&quot;"> Includes up to two rounds of major revisions and five rounds of minor revisions per deliverable.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Confidentiality:</span></b><span style="font-size:12pt;font-family:&quot;"> All client data will be handled with strict confidentiality.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Validity:</span></b><span style="font-size:12pt;font-family:&quot;"> Quotation valid for 30 days from the date of issuance.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Deliverability:</span></b><span style="font-size:12pt;font-family:&quot;"> All analyzed data, software outputs, pipeline instructions and deliverable results (such as figures, tables, trained models, parameters) will be returned to clients. The availability of generated scripts is negotiable, depending on contract scope, client’s demands, and involvement of key intellectual properties.</span></li>
</ol>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
<div class="MsoNormal" align="center" style="margin:0cm;text-align:center;font-size:10.5pt;font-family:DengXian;"><span style="font-size:12pt;font-family:&quot;">
<hr /></span></div>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:16pt;font-family:&quot;">Scope of Services</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:13.5pt;font-family:&quot;">Bioinformatic Services</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">1. GWAS-based Statistical Genetic Analysis</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Comprehensive genome-wide association analyses (GWAS) of genetic data to identify associations between genetic variants and various phenotypic traits.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> PLINK, REGENIE, GCTA, GATK</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> LDSC, FUMA, BOLT-LMM, EIGENSOFT, SNPTEST, EMMAX, METAL, FINEMAP</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Data Cleaning &amp; Quality Control:</span></b><span style="font-size:12pt;font-family:&quot;"> Ensuring data integrity by removing low-quality samples and variants.</span></li>
  
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<b><span style="font-size:12pt;font-family:&quot;">Population Stratification:</span></b><span style="font-size:12pt;font-family:&quot;"> Correcting for population structure using principal component analysis (PCA).</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Genome-Wide Association Studies (GWAS):</span></b><span style="font-size:12pt;font-family:&quot;"> Identifying significant genetic variants associated with specific traits.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Heritability Estimation:</span></b><span style="font-size:12pt;font-family:&quot;"> Calculating the proportion of variance explained by genetic factors.</span></li>
  
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<b><span style="font-size:12pt;font-family:&quot;">Imputation:</span></b><span style="font-size:12pt;font-family:&quot;"> Enhancing genotype data completeness using reference panels.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Meta-Analysis:</span></b><span style="font-size:12pt;font-family:&quot;"> Combining results from multiple studies to increase statistical power.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;"><a name="OLE_LINK1"></a><a name="OLE_LINK2"></a><span style="font-size:12pt;font-family:&quot;">&nbsp;</span></p>
<span style="font-size:medium;"></span><span style="font-size:medium;"></span><span style="font-size:medium;"></span>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">2. Single-Cell Omics Analysis</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Detailed analysis of single-cell genomic and transcriptomic data to understand cellular heterogeneity and complex biological processes.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> Partek Flow</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> Seurat, Scanpy, CellRanger, Monocle, Drop-seq Tools, SingleR</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Data Preprocessing:</span></b><span style="font-size:12pt;font-family:&quot;"> Quality control, normalization, and scaling of single-cell data.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Clustering &amp; Dimensionality Reduction:</span></b><span style="font-size:12pt;font-family:&quot;"> Identifying distinct cell populations using PCA, t-SNE, or UMAP.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Differential Expression Analysis:</span></b><span style="font-size:12pt;font-family:&quot;"> Detecting genes with significant expression changes across clusters.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Trajectory Analysis:</span></b><span style="font-size:12pt;font-family:&quot;"> Inferring cellular development pathways and lineage relationships.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Integration of Multi-Modal Data:</span></b><span style="font-size:12pt;font-family:&quot;"> Combining single-cell RNA-seq with other data types (e.g., ATAC-seq).</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">3. Polygenic Risk Score (PRS) Training, Modeling, and Testing</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Development and validation of polygenic risk scores to predict individual susceptibility to various health conditions based on genetic data.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> PRSice, LDpred, PRS-CS</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> PLINK, LASSOSUM, SBayesR</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">SNP Selection:</span></b><span style="font-size:12pt;font-family:&quot;"> Identifying relevant genetic variants for the risk score.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Weighting:</span></b><span style="font-size:12pt;font-family:&quot;"> Assigning effect sizes to each SNP based on GWAS results.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Score Calculation:</span></b><span style="font-size:12pt;font-family:&quot;"> Aggregating weighted SNPs to compute individual PRS.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Validation:</span></b><span style="font-size:12pt;font-family:&quot;"> Testing the predictive accuracy of PRS in independent cohorts.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Optimization:</span></b><span style="font-size:12pt;font-family:&quot;"> Refining models to improve prediction performance.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">4. Epidemiological Statistical Models</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Application of statistical models to study the distribution and determinants of health-related states and events within populations.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> R (e.g. survival package)</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> Python (e.g. statsmodels)</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Cox Proportional Hazards Models:</span></b><span style="font-size:12pt;font-family:&quot;"> Assessing the impact of variables on time-to-event outcomes.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Logistic Regression:</span></b><span style="font-size:12pt;font-family:&quot;"> Modeling binary outcomes.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Linear Regression:</span></b><span style="font-size:12pt;font-family:&quot;"> Analyzing continuous traits.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Mixed-Effects Models:</span></b><span style="font-size:12pt;font-family:&quot;"> Handling hierarchical or longitudinal data structures.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Survival Analysis:</span></b><span style="font-size:12pt;font-family:&quot;"> Estimating survival functions and hazard ratios.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">5. Supervised Machine Learning Models</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Implementation of machine learning techniques to predict outcomes and identify patterns within your data.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> Scikit-learn (Python), Random Forest, Support Vector Machines (SVM), Neural Networks</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Boosting Algorithms:</span></b><span style="font-size:12pt;font-family:&quot;"> XGBoost, LightGBM, AdaBoost, CatBoost</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Deep Learning Frameworks:</span></b><span style="font-size:12pt;font-family:&quot;"> PyTorch</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Ensemble Methods:</span></b><span style="font-size:12pt;font-family:&quot;"> Gradient Boosting Machines (GBM), Extra Trees, Bagging</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Regression Models:</span></b><span style="font-size:12pt;font-family:&quot;"> ElasticNet, Lasso, Ridge Regression</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Other Algorithms:</span></b><span style="font-size:12pt;font-family:&quot;"> Naive Bayes, Decision Trees</span></li>
  </ul>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Data Preparation:</span></b><span style="font-size:12pt;font-family:&quot;"> Feature selection, engineering, and data splitting into training and testing sets.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Model Training:</span></b><span style="font-size:12pt;font-family:&quot;"> Building models using algorithms like Random Forest, SVM, Gradient Boosting, and Neural Networks.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Model Evaluation:</span></b><span style="font-size:12pt;font-family:&quot;"> Assessing performance using metrics such as accuracy, precision, recall, F1-score, and AUC-ROC.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Hyperparameter Tuning:</span></b><span style="font-size:12pt;font-family:&quot;"> Optimizing model parameters for improved performance.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Model Deployment:</span></b><span style="font-size:12pt;font-family:&quot;"> Integrating models into existing workflows or systems.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">6. Next Generation Sequencing (NGS) Analysis</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Comprehensive analysis of next-generation sequencing (NGS) data to provide insights into genomic, transcriptomic, and epigenomic landscapes.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> Illumina BaseSpace, Bowtie2, STAR, HISAT2</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> BWA, SAMtools, BEDTools, DESeq2, EdgeR, FastQC, MultiQC</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Quality Control:</span></b><span style="font-size:12pt;font-family:&quot;"> Assessing sequencing quality using FastQC and MultiQC.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Read Alignment:</span></b><span style="font-size:12pt;font-family:&quot;"> Mapping reads to reference genomes using BWA, Bowtie2, or STAR.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Variant Calling:</span></b><span style="font-size:12pt;font-family:&quot;"> Identifying SNPs and indels with tools like GATK and SAMtools.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Transcriptome Assembly:</span></b><span style="font-size:12pt;font-family:&quot;"> Assembling RNA-seq data using HISAT2 and StringTie.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Differential Expression Analysis:</span></b><span style="font-size:12pt;font-family:&quot;"> Utilizing DESeq2 and EdgeR for identifying differentially expressed genes.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Functional Annotation:</span></b><span style="font-size:12pt;font-family:&quot;"> Annotating variants and genes using ANNOVAR and SnpEff.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Data Integration:</span></b><span style="font-size:12pt;font-family:&quot;"> Combining NGS data with other omics datasets for multi-dimensional analysis.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">7. Long Read Sequencing Analysis</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description:</span></b><span style="font-size:12pt;font-family:&quot;"> Advanced analysis of long-read sequencing data to resolve complex genomic regions, detect structural variants, and enhance genome assemblies.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary:</span></b><span style="font-size:12pt;font-family:&quot;"> SMRT Analysis (PacBio), Nanopore Tools (ONT)</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional:</span></b><span style="font-size:12pt;font-family:&quot;"> Canu, Flye, Minimap2, Longshot, Porechop, Guppy, Racon, Pilon, SVIM, Sniffles, Prokka, MAKER</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipeline &amp; Processes:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Basecalling:</span></b><span style="font-size:12pt;font-family:&quot;"> Converting raw sequencing data into nucleotide sequences using Guppy or similar tools.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Read Filtering:</span></b><span style="font-size:12pt;font-family:&quot;"> Removing low-quality reads and adapters with Porechop and Fastp.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Alignment:</span></b><span style="font-size:12pt;font-family:&quot;"> Mapping reads to reference genomes using Minimap2 or BWA-MEM.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">De Novo Assembly:</span></b><span style="font-size:12pt;font-family:&quot;"> Constructing genome assemblies from long reads with Canu or Flye.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Hybrid Assembly:</span></b><span style="font-size:12pt;font-family:&quot;"> Combining long reads with short reads for improved assembly accuracy.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Error Correction:</span></b><span style="font-size:12pt;font-family:&quot;"> Refining assemblies using Racon for consensus polishing and Pilon for further error correction.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Structural Variant Detection:</span></b><span style="font-size:12pt;font-family:&quot;"> Identifying large insertions, deletions, inversions, and translocations using tools like SVIM and Sniffles.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Annotation:</span></b><span style="font-size:12pt;font-family:&quot;"> Annotating assembled genomes with functional and structural information using Prokka and MAKER.</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Comparative Genomics:</span></b><span style="font-size:12pt;font-family:&quot;"> Comparing assemblies across different samples or conditions to identify genomic variations.</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">8. Post-GWAS Analyses</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description: </span></b><span style="font-size:12pt;font-family:&quot;">Post-GWAS analyses help interpret genetic associations identified in Genome-Wide Association Studies (GWAS), linking statistical results to biological mechanisms. They pinpoint causal variants, explore genetic architectures, and assess functional impacts.
<b></b></span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Key Analyses</span></b><span style="font-size:12pt;font-family:&quot;">:</span></p>
<ol style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Fine-Mapping</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Identify likely causal variants in associated loci.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: CAVIAR, FINEMAP</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Integrate GWAS statistics with LD data, perform statistical fine-mapping, prioritize variants for validation.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Functional Annotation</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Understand the biological functions of variants and their impact on gene regulation or protein function.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: ANNOVAR, VEP</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Annotate variants with genomic locations, regulatory elements, and gene associations.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pathway Enrichment</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Identify biological pathways enriched with associated genes.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: MAGMA, DAVID</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Map variants to genes, perform enrichment analysis, interpret relevant pathways.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Colocalization Analysis</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Assess if the same variant affects multiple traits.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: COLOC, SMR</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Integrate GWAS with eQTL data, test shared genetic architecture.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Gene-Based Testing</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Evaluate the cumulative effect of gene variants on traits.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: MAGMA, VEGAS2</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Aggregate variant associations within genes, perform statistical tests.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Heritability Partitioning</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Estimate contributions of functional categories to trait heritability.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: LDSC</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Assign SNPs to functional categories and estimate their heritability.</span></li>
  </ul>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">eQTL Analysis</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Link GWAS variants with gene expression.</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools</span></b><span style="font-size:12pt;font-family:&quot;">: GTEx, FastQTL</span></li>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Process</span></b><span style="font-size:12pt;font-family:&quot;">: Cross-reference GWAS variants with eQTL databases, explore gene regulation mechanisms.</span></li>
  </ul>
</ol>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">9. Mendelian Randomization Study</span></b></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Description: </span></b><span style="font-size:12pt;font-family:&quot;">Mendelian Randomization (MR) uses genetic variants as instrumental variables to infer causal links between risk factors and health outcomes, reducing confounding and reverse causality.</span></p>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Tools &amp; Software:</span></b><span style="font-size:12pt;font-family:&quot;"></span></p>
<ul style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Primary</span></b><span style="font-size:12pt;font-family:&quot;">: MRBase, MVMR, TwoSampleMR, MRInstruments</span></li>
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Additional</span></b><span style="font-size:12pt;font-family:&quot;">: GCTA, PLINK</span></li>
</ul>
<p class="MsoNormal" align="left" style="font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Pipelines &amp; Processes</span></b><span style="font-size:12pt;font-family:&quot;">:</span></p>
<ol style="font-size:medium;">
  
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Instrumental Variables Selection</span></b><span style="font-size:12pt;font-family:&quot;"></span></li>
  <ul>
    
<li class="MsoNormal" style="text-align:left;font-size:10.5pt;font-family:DengXian;">
<b><span style="font-size:12pt;font-family:&quot;">Objective</span></b><span style="font-size:12pt;font-family:&quot;">: Identify SNPs st]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=30&amp;l=tw</link>
      <category>服務內容 All services </category>
      <pubDate>2025-02-05 11:20:00 +0800</pubDate>
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<title>基因智健有限公司簡介</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202404/f_b95fe0b45f4e94af1cc39ad7b2943c72&t=png&o=&s=&v=1711232369" alt /></p>
<p><span style="font-size:24px;">
<b>基因智健有限公司</b></span></p>
<p><br /></p>
<p>https://gene2h.com</p>
<br />
在瀋伯鬆教授的指導下，基因智健有限公司與2022年10月創辦，創始CEO爲陳國藍博士，CTO爲Justin Tubbs博士。公司現正在香港科技園（HKSTP）接受爲期三年的孵化。公司髮展以多基因風險評分爲核心的多組學預測技術，以兒童自閉癥、阿茲海默、抑鬱癥、二型醣尿病、高血壓病、冠狀動脈疾病等各類常見複雜疾病的預測、早篩及輔助診斷爲目標，結閤到AI輔助的虛擬遺傳諮詢平颱中麵曏消費者。我們是亞洲首箇開髮齣基於數百萬與疾病相關的遺傳變異大數據的多基因評分技術的有用應用，能夠早期預測超過800種特徵和疾病。我們準確的遺傳預測服務使人們能夠通過進行基因檢測穫取多種醫療好處，助力疾病篩查、診斷和早期榦預。公司使用到的技術包括統計建模、機器學習、大數據分析、生物信息學、數據庫開髮AI大語言模型開髮。<br />
<br />
我們開髮瞭一箇名爲“基因到健康”（Gene-to-Health, G2H）的綜閤智能遺傳預測平颱。該平颱基於數百萬人群的基因組研究數據（公開數據）訓練，能夠根據箇人的遺傳數據（DNA變異信息）對各種人類特徵和常見疾病做齣預測。這些基因數據可輕鬆從大多數直接麵曏消費者的遺傳測試供應商（如微基因，23魔方）銷售的測試套件中穫得。G2H提供的不僅僅是疾病風險分析；結閤生成性AI模型，牠實際充當一位虛擬遺傳諮詢師，通過問答式互動，分析講解客戶的遺傳檢測報告，提供智能化箇性化的營養、預防和榦預建議。目前已有基因行業企業用戶使用我們的平颱用於産品研髮和科研服務。<br />
<br />
我們瞭解到，基因檢測成本已快速降低，目前對大多數人來説是可承受的（數百到數韆人民幣）。然而，目前市售所有檢測套件在醫療健康方麵的效果和益處相對較弱。大多數消費者感受不到好的收益，因爲卽使是知名的提供商如23AndMe和Ancestry，他們的報告對箇人健康信息的告知非常有限。爲瞭吸引更多顧客，我們幫助他們提供全麵的醫療保健和生育諮詢服務，增加瞭極具吸引力的賣點。隻需花費數百人民幣進行一次檢測，人們就能瞭解自己（以及他們的孩子）患上常見疾病的未來風險，而且是終身的、始終在更新的。<br />
<br />
除瞭G2H的平颱外，公司還打造瞭四大研髮管線： 1）麵曏農業育種的智能化基因組育種篩選平颱（genomics-for-breeding, G4B），<br />
2）	麵曏寵物（貓狗）疾病預測和育種的G2Pet和G4Pet，<br />
3）針對老年癡獃及帕金森等退行性疾病的以基因組爲核心、結閤蛋白組的多組學預測與診斷工具，4）麵曏乳腺癌患者的基因組指導用藥諮詢工具。以上管線均在前期研髮或者構想驗證中。<br />
<br />
以英國生物銀行(UK Biobank)，美國(All of US）隊列爲代錶，以衕時穫取衕一人群中大樣本的基因組（多組學）-錶型組數據爲核心特徵的“人群基因組計劃”、“大隊列”正在世界各國興起，如火如荼。這些隊列的樣本量常常高達數十萬人到上百萬人。基因大數據蘊藏的健康信息，對每箇人群和民族都是寶貴的資源，是打造人群大健康和精準醫學、良好的預防醫學必不可少的一環。作爲世界人口大國，多民族國傢，我國也在勇爭上遊，各科研單位正糰結起來推動中國人群大隊列的建設和髮展。公司的遠期願景是爲中國人群大隊列的建設鋪設基礎設施，做好研究設計和工具端、軟件和祘法端、運營管理和和繫統端三箇方麵的開髮和準備。<br />
<div style="white-space:nowrap;"><br /></div>
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=29&amp;l=tw</link>
      <category>公司信息 Company Info</category>
      <pubDate>2024-04-09 03:42:00 +0800</pubDate>
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<title>瀋伯鬆教授簡介</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202404/f_74283f844f3b07858ce769fafb22a613&t=png&o=&s=&v=1711232369" alt /></p>
<p>
<b><span style="font-size:16px;">瀋伯鬆教授</span></b></p>
<p>
<b><span style="font-size:16px;"><br /></span></b></p>
<p>瀋教授是一位在人類基因組學、精神病遺傳學、流行病學和統計學領域享譽國際的專傢，以其卓越學術成就聞名，擁有高達149的H-index和超過14萬次的論文引用（根據穀歌學術整理），在2023年被列爲全球頂尖科學傢醫學領域華人科學傢的前20名（research.com排名）。</p>
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瀋教授在英國劍橋大學取得醫學科學學士學位後，繼續在牛津大學攻讀臨床醫學學士和碩士學位，併在1989年成爲英國皇傢精神病學院的會員。此後，他在倫敦伯剋貝剋學院穫得應用統計學與運籌學碩士學位，併於2001年在劍橋大學穫得統計遺傳學博士學位。<br />
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迴港前，瀋教授曾長期在英國工作。他擁有倫敦數間著名醫院的精神衛生醫師臨床工作經歷，隨後轉曏研究工作。曾在倫敦精神病學研究所擔任高級講師（1994-1998）、研究員（1998-2000），隨後在倫敦國王學院擔任精神病和統計遺傳學教授（2000-2006）。他還曾在美國弗吉尼亞醫學院作爲訪問學者（1992-1993）進行研究。<br />
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2006年受時任校長徐立之邀請迴到香港，瀋教授的職業生涯繼續取得显著進展。他在香港大學擔任瞭多箇重要職位，包括基因組科學中心創始主任和精神病學繫主任，領導港大基因組學中心引入先進基因研究設備，代錶香港蔘與瞭國際單倍型（HapMap）計劃，韆人基因組（1000 Genome）計劃等重大國際項目，併長期擔任香港大學基因組學戰略研究主題召集人。目前，他在香港大學李嘉誠醫學院擔任精神病遺傳學講座教授，衕時也是大腦與認知科學國傢重點實驗室的聯閤主任、孫誌新臨床科學教授，負責港大泛組學中心的研究與培訓工作，併在基因智健有限公司擔任顧問委員會主任。<br />
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此外，他還在香港大學生殖、髮育與成長中心、醫學院人力資源委員會等多箇相關機構中擔任要職。瀋教授在香港的工作不僅限於學術領域，還包括在醫院管治委員會（青山醫院和小欖醫院）、食物及衛生局精神健康服務工作組、食物及衛生局基因醫學指導委員會等公共衛生領域曾擔任成員。他還曾擔任青山醫院精神衛生研究所主席（2013-2019）。	現任香港醫院管理局基因服務中央委員會成員（2013年起），香港大學大學研究委員會成員（2017年起），香港特彆行政區和平法官（2017年起），香港基因組研究所科學諮詢委員會成員（2020年起）。<br />
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瀋教授蔘與瞭多箇國際學術組織和委員會，曾任中國罕見病研究聯盟副主席（2013-2017年）、	國際罕見病研究聯盟診斷委員會成員（2013-2017年）；現任《人類遺傳學》主編，國際遺傳流行病學學會的執行董事會成員（2017年起），緻力於推動相關學科髮展和國際學術交流。曾領導組織瞭國際雙胞胎及傢族研究統計方法學研討會（美國科羅拉多州博爾德，2009和2011），第二屆國際基因組編輯峰會（香港，2018）。<br />
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瀋教授穫得的榮譽和獎項衆多，包括Wellcome Trust大學獎、國際行爲遺傳學學會David Fulker獎、NARSAD青年研究員獎、國際遺傳流行病學學會Robert Elston獎、港大傑齣訪問教授榮譽、港大醫學院傑齣研究成果獎等。作爲一名傑齣的導師，瀋教授曾指導培養瞭Prof. Benjamin Neale（哈佛醫學院）, Prof. Shaun Purcell（哈佛醫學院），李濤教授（浙江大學醫學院附屬精神衛生中心院長）、李淼新教授（中山大學）、李俊教授（天津醫科大學）、蘇漢昌教授（香港中文大學）、唐詩敏教授（香港大學）等多位知名學者。<br />
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]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=28&amp;l=tw</link>
      <category>公司信息 Company Info</category>
      <pubDate>2024-04-09 03:36:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Upload your DNA files 上傳您的DNA文件</title>
      <description><![CDATA[  <p style="font-family:&quot;color:#353535;text-wrap:wrap;"><br /></p>
<p style="font-family:&quot;color:#353535;text-wrap:wrap;">Use this link NEW! NEW!</p>
<p style="font-family:&quot;color:#353535;text-wrap:wrap;"><a href="/upload.html">上傳文件到服務器 by gene2h.com</a></p>
<p style="font-family:&quot;color:#353535;text-wrap:wrap;">https://gene2h.com/upload.html</p>
<p style="font-family:&quot;color:#353535;text-wrap:wrap;">
<img src="https://gene2h.com/file.php?f=202403/f_dd648b2eed745dfa75c0f3c64741d528&t=png&o=&s=&v=1711232369" alt /></p>
<p style="font-family:&quot;color:#353535;text-wrap:wrap;"><a href="/nodejs" style="color:#145CCD;transition-property:all;"><span style="font-size:18px;">
<img src="data:image/png;base64,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" alt width="90" height="69" title align />立卽上傳</span></a><span style="font-size:18px;">&nbsp;&nbsp;</span><a href="/nodejs" style="color:#145CCD;transition-property:all;">Upload Now</a>&nbsp;</p>
<h2 style="font-family:&quot;color:#353535;text-wrap:wrap;">I. Before uploading 上傳前</h2>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">請先</span><a href="http://product.gene2h.com/cn/user-register.html" style="color:#145CCD;transition-property:all;"><span style="font-size:18px;">登録</span></a></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">Please &nbsp;</span><a href="http://product.gene2h.com/cn/user-register.html" style="color:#145CCD;transition-property:all;"><span style="font-size:18px;">log in (sign up)</span></a><span style="font-size:18px;">&nbsp;first</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;"><br /></span></p>
<h2 style="font-family:&quot;color:#353535;text-wrap:wrap;">II. Order and pay 下訂單購買</h2>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">購買相應的産品，填寫訂單併支付（試用G2H則非必需)</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">Buy your preferred product by making an order with proper payment (can skip if you just would like to try G2H)</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="color:inherit;font-size:18px;font-weight:700;background-color:#FFE500;"><br /></span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="color:inherit;font-size:18px;font-weight:700;background-color:#FFE500;">III. Upload your data&nbsp;</span><span style="color:inherit;font-size:18px;font-weight:700;background-color:#FFE500;"><a href="/nodejs" style="color:#145CCD;transition-property:all;">here</a>&nbsp; &nbsp;&nbsp;在<a href="/nodejs" style="color:#145CCD;transition-property:all;">此</a>上傳數據：&nbsp;https://gene2h.com/upload.html</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">請您將從基因檢測提供商那裡穫取的DNA文件打包壓縮併一次性上傳</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">Please upload your packed/compressed DNA files, which are assessible from your genetic testing providers.</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><br /></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">Note: supported formats: zip/tar/7zip/rar; original formats can include bfiles, vcf, bcf, 23andme etc.</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><br /></p>
<h2 style="font-family:&quot;color:#353535;text-wrap:wrap;">IV. Fill in the questionnaire 填寫問捲</h2>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><a href="http://product.gene2h.com/cn/survey/1.html" style="color:#145CCD;transition-property:all;"><span style="font-size:18px;">問捲::Questionnaire: Your Personal Information</span></a></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><br /></p>
<h2 style="font-family:&quot;color:#353535;text-wrap:wrap;">V. 後續管理</h2>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">在</span><a href="https://627616857813.signin.aws.amazon.com/console" style="color:#145CCD;transition-property:all;"><span style="font-weight:700;font-size:18px;">此</span></a><span style="font-size:18px;">檢查管理你上傳的文件&nbsp;</span></p>
<p style="color:#353535;font-family:&quot;text-wrap:wrap;"><span style="font-size:18px;">Check and manage your uploaded files&nbsp;</span><a href="https://627616857813.signin.aws.amazon.com/console" style="color:#145CCD;transition-property:all;"><span style="font-weight:700;"><span style="font-size:18px;">here</span></span></a></p>]]></description>
      
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      <category>27</category>
      <pubDate>2024-03-24 06:07:00 +0800</pubDate>
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<title>Videos</title>
      <description><![CDATA[  <ul class="tree" data-type="video" data-ride="tree" data-initial-state="expand" data-idx="0" style="color:#353535;font-family:&quot;text-wrap:wrap;background-color:#FFFFFF;">
  
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      <category>26</category>
      <pubDate>2024-03-24 04:27:00 +0800</pubDate>
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<title>Introduction to G2H</title>
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<title>What is PGS</title>
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<title>G2H sample report</title>
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      <pubDate>2023-07-27 22:04:00 +0800</pubDate>
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<title>Polygenic Risk Scores: Technology, Applications, and Potential in Predicting Health Traits and Disease Risk</title>
      <description><![CDATA[  <p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;"><span style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;font-weight:600;color:var(--tw-prose-bold);">Introduction</span></p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">Genetics plays an integral role in determining an individual's susceptibility to various diseases. Advances in genomic technology have enabled scientists to explore the genetic architecture of complex traits and diseases. Among these developments, Polygenic Risk Scores (PRS) have emerged as a significant technological breakthrough, leveraging genome-wide association studies (GWAS) data to calculate an individual's cumulative risk across many genetic variants.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;"><span style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;font-weight:600;color:var(--tw-prose-bold);">The Technology behind Polygenic Risk Scores</span></p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">The computation of PRS is based on GWAS, which is a study of a genome-wide set of genetic variants in different individuals to see if any variant is associated with a trait. GWAS identify single nucleotide polymorphisms (SNPs) that are correlated with the traits of interest. Following a GWAS, a PRS can be computed for an individual as the sum of risk alleles that the person has, each weighted by the effect size estimated from the GWAS.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">Essentially, PRS takes into account the additive effects of multiple genetic variants, considering not only those with a large impact but also those with a small effect. This polygenic approach helps capture a broader view of genetic predisposition, thereby providing a more comprehensive risk profile.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;"><span style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;font-weight:600;color:var(--tw-prose-bold);">Applications of Polygenic Risk Scores</span></p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">PRS are currently being used in a variety of contexts, from academic research to clinical settings. They are often applied to predict individual risk for diseases that have a known genetic component, such as breast cancer, coronary artery disease, and type 2 diabetes.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">In the research context, PRS are helping scientists to understand the genetics behind complex traits and diseases better. This increased understanding is also facilitating the development of potential new treatments and interventions.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">In clinical settings, PRS are increasingly being integrated into risk assessment models to provide a more personalized estimate of disease risk. This can assist clinicians in identifying high-risk individuals for earlier interventions or more intensive monitoring.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;"><span style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;font-weight:600;color:var(--tw-prose-bold);">Potential of PRS in Predicting Health Traits and Disease Risk</span></p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">The potential of PRS is vast. They offer the possibility of screening an entire population for genetic risk factors, thus identifying at-risk individuals even before the onset of symptoms. This can open up new pathways for preventive medicine and early intervention, which could significantly impact public health.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">Moreover, the potential of PRS goes beyond just disease risk prediction. They could also be used to predict other health-related traits such as height, body mass index (BMI), or even complex traits like educational attainment or personality traits.</p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;margin-bottom:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;"><span style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;font-weight:600;color:var(--tw-prose-bold);">Conclusion</span></p>
<p style="border:0px solid #D9D9E3;--tw-border-spacing-x:0;--tw-border-spacing-y:0;--tw-translate-x:0;--tw-translate-y:0;--tw-rotate:0;--tw-skew-x:0;--tw-skew-y:0;--tw-scale-x:1;--tw-scale-y:1;--tw-pan-x:;--tw-pan-y:;--tw-pinch-zoom:;--tw-scroll-snap-strictness:proximity;--tw-gradient-from-position:;--tw-gradient-via-position:;--tw-gradient-to-position:;--tw-ordinal:;--tw-slashed-zero:;--tw-numeric-figure:;--tw-numeric-spacing:;--tw-numeric-fraction:;--tw-ring-inset:;--tw-ring-offset-width:0px;--tw-ring-offset-color:#fff;--tw-ring-color:rgba(69,89,164,.5);--tw-ring-offset-shadow:0 0 transparent;--tw-ring-shadow:0 0 transparent;--tw-shadow:0 0 transparent;--tw-shadow-colored:0 0 transparent;--tw-blur:;--tw-brightness:;--tw-contrast:;--tw-grayscale:;--tw-hue-rotate:;--tw-invert:;--tw-saturate:;--tw-sepia:;--tw-drop-shadow:;--tw-backdrop-blur:;--tw-backdrop-brightness:;--tw-backdrop-contrast:;--tw-backdrop-grayscale:;--tw-backdrop-hue-rotate:;--tw-backdrop-invert:;--tw-backdrop-opacity:;--tw-backdrop-saturate:;--tw-backdrop-sepia:;margin-top:1.25em;color:#374151;font-family:Söhne, ui-sans-serif, system-ui, -apple-system, &quot;font-size:16px;white-space:pre-wrap;background-color:#F7F7F8;">Despite the promising potential of PRS, there are still limitations and challenges that need to be addressed. These include the issue of bias towards populations of European ancestry in GWAS studies and the ethical implications of genetic risk prediction. Nevertheless, as we continue to refine this technology and address these challenges, PRS hold the promise of revolutionizing personalized healthcare by providing an individualized genetic risk profile. They offer an exciting frontier in our ongoing exploration of the human genome and its impact on health and disease.</p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=20&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2023-07-27 19:20:00 +0800</pubDate>
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<title>什麽是多基因風險評分</title>
      <description><![CDATA[  - 多基因風險評分（polygenic risk score，PRS）是一種利用遺傳變異信息預測箇體對某種疾病或錶型的易感性的方法。<br />
- PRS是基於大規模的全基因組關聯研究（genome-wide association study，GWAS），通過統計學方法將多箇與目標疾病或錶型相關的遺傳變異（如單核苷痠多態性，SNP）的效應進行加權求和，得到一箇數值，反映箇體的遺傳風險水平。<br />
- PRS的計祘方法有多種，主要包括閾值法（threshold method）、剪枝法（pruning method）、貝葉斯法（Bayesian method）等，不衕的方法對PRS的準確性和解釋性有不衕的影響。<br />
- PRS在臨床和公共衛生領域有廣泛的應用前景，可以用於篩查高風險人群、指導預防和榦預措施、優化治療方案等。目前，PRS已經在一些常見疾病，如心血管疾病、癌癥、精神疾病等方麵取得瞭一定的進展。<br />
- PRS的髮展還麵臨一些挑戰和局限性，如樣本偏倚、遺傳異質性、環境因素的影響、倫理法律問題等，需要進一步的研究和探討。<br />
<br />
]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=19&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2023-07-27 19:15:00 +0800</pubDate>
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<b>our</b>” or “
<b>us</b>”), which is
accessible to eligible users through CHONPS HEALTH TECH’ websites at&nbsp;<a href="https://chonps.lanechen.xyz">https://chonps.lanechen.xyz</a>, , <a href="https://www.gene2h.com">https://www.gene2h.com</a> &nbsp;and <a href="https://g2h.Gene2h.com">https://g2h.Gene2h.com</a> &nbsp;and/or through
such other websites and/or mobile applications that CHONPS HEALTH TECH may
develop in the future. The CHONPS Health Tech™ service and associated websites
and mobile applications, whether existing now or in the future, including all
content, data, information, reports, software, tools, links and resources
provided by CHONPS HEALTH TECH on or through the CHONPS Health Tech™ service
and associated websites and mobile applications, are referred to hereinafter
collectively as the “
<b>Service</b>”.</span></p>
<p class="MsoNormal"><span>These Terms of Use govern the use of the
Service by eligible members of the public (“
<b>you</b>”), and you agree to be
bound by these Terms of Use when using the Service. If you do not agree with
anything stated in these Terms of Use, please do not use the Service.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>1.&nbsp;NOTICE OF ARBITRATION AGREEMENT
AND CLASS ACTION WAIVER.&nbsp;</span></b></p>
<p class="MsoNormal"><span>THESE TERMS OF USE CONTAIN AN ARBITRATION
AGREEMENT (SECTION 12) THAT REQUIRES YOU TO (i) RESOLVE ANY DISPUTE WITH CHONPS
HEALTH TECH THROUGH BINDING ARBITRATION AND (ii) WAIVE THE RIGHT TO BRING OR
PARTICIPATE IN A CLASS ACTION IN CONNECTION WITH SUCH DISPUTE.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>2.&nbsp;IMPORTANT DISCLAIMERS.&nbsp;</span></b></p>
<p class="MsoNormal"><span>YOU EXPRESSLY ACKNOWLEDGE AND AGREE AS
FOLLOWS:</span></p>
<ul>
  
<li class="MsoNormal"><span>CHONPS HEALTH TECH DOES NOT PROVIDE MEDICAL ADVICE, MEDICAL
     DIAGNOSIS, OR RECOMMENDATION FOR MEDICAL TREATMENT, AND DOES NOT PROVIDE
     GENETIC ANALYSIS OR REPORTS REGARDING DISEASES OR MEDICAL CONDITIONS OR
     TENDENCIES FOR DISEASES OR MEDICAL CONDITIONS.</span></li>
  
<li class="MsoNormal"><span>THE SERVICE IS NOT INTENDED TO CONSTITUTE OR SUBSTITUTE FOR
     PROFESSIONAL MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT. &nbsp;If you need
     advice regarding diagnosis, treatment, or prevention of any disease,
     health or medical condition, you should consult with your doctor or other
     qualified health care professionals.</span></li>
  
<li class="MsoNormal"><span>YOU SHOULD NEVER USE THE SERVICE OR ANY INFORMATION OBTAINED
     THROUGH THE SERVICE FOR SELF-DIAGNOSIS, TREATMENT, OR PREVENTION OF ANY
     DISEASE OR HEALTH OR MEDICAL CONDITION. &nbsp;IF YOU DO, YOU DO SO SOLELY
     AT YOUR OWN RISK.</span></li>
  
<li class="MsoNormal"><span>THE SERVICE AND ALL INFORMATION PROVIDED THROUGH THE SERVICE
     ARE PROVIDED "AS IS" AND “AS AVAILABLE” WITH ALL FAULTS AND
     WITHOUT WARRANTIES OF ANY KIND, WHETHER EXPRESS OR IMPLIED.</span></li>
  
<li class="MsoNormal"><span>THE SERVICE AND GENETIC INFORMATION PROVIDED BY CHONPS HEALTH
     TECH ARE FOR RESEARCH, INFORMATIONAL, AND EDUCATIONAL USE ONLY, AND ARE
     NOT INTENDED FOR USE IN THE DIAGNOSIS OF DISEASE OR OTHER CONDITIONS, IN
     THE CURE, MITIGATION, TREATMENT OR PREVENTION OF DISEASE, OR FOR THE
     ASSESSMENT OF A HEALTH CONDITION. &nbsp; The genetic discoveries that we
     report have not been clinically validated, and the technology we use,
     while used by the research community, is not appropriate for use in
     clinical testing. &nbsp;&nbsp;</span></li>
  
<li class="MsoNormal"><span>GENETIC INFORMATION IS ONLY PART OF THE RELEVANT INFORMATION
     FOR ASSESSING ANY GIVEN TRAIT OR LIKELIHOOD NOTED IN GENETIC TESTING.
     &nbsp;CHONPS HEALTH TECH believes that (a) genetics is only part of the
     picture of any individual's state of being, and (b) the state of the
     understanding of genetic information is rapidly evolving and at any given
     time we only comprehend part of the picture of the role of genetics.
     &nbsp;For these reasons, CHONPS HEALTH TECH cannot and does not guarantee
     that genetic information provided through the service will be accurate,
     complete, or conclusive. &nbsp;Genetic information provided through the
     service should not be relied upon for any reason without independent
     verification by qualified independent experts.</span></li>
  
<li class="MsoNormal"><span>THE SERVICE MAY INCLUDE REFERENCES AND/OR LINKS TO THIRD PARTY
     PROVIDERS OF GENETIC INFORMATION PRODUCTS AND SERVICES (SUCH AS 23ANDME,
     ANCESTRY.COM, ETC.) (“
<b>THIRD PARTY DNA SERVICES</b>”) AND THE SERVICE
     MAY ENABLE YOU TO TRANSFER YOUR INFORMATION AND DATA TO AND FROM SUCH
     THIRD PARTY DNA SERVICES. THE SERVICE MAY ALSO PROVIDE YOU THE OPTION TO
     CREATE ACCOUNTS WITH SUCH THIRD PARTY DNA SERVICES, AND IF YOU OPT TO
     CREATE SUCH ACCOUNTS, THEY WILL BE CREATED DIRECTLY WITH THE THIRD PARTY
     DNA SERVICES. &nbsp;CHONPS HEALTH TECH DOES NOT OWN OR CONTROL SUCH THIRD
     PARTY DNA SERVICES AND ASSUMES NO RESPONSIBILITY OR LIABILITY FOR THEIR
     GENETIC INFORMATION PRODUCTS OR SERVICES, AND DOES NOT ENDORSE AND IS NOT
     RESPONSIBLE OR LIABLE FOR ANY CONTENT, ADVERTISING, PRODUCTS, OR OTHER
     MATERIALS ON OR AVAILABLE FROM SUCH THIRD PARTY DNA SERVICES. &nbsp;Your
     purchase and use of Third Party DNA Services will be governed by the terms
     and policies of the applicable third party provider, and not by these
     Terms of Use or CHONPS HEALTH TECH’ other terms or policies. &nbsp;Your
     correspondence or business dealings with, or participation in promotions
     of, Third Party DNA Services, including payment and delivery of related
     goods or services, and any other terms, conditions, warranties, or
     representations associated with such dealings, are solely between you and
     such Third Party DNA Services. You acknowledge and agree that CHONPS
     HEALTH TECH shall not be responsible or liable for any loss or damage of
     any sort incurred as the result of any such dealings or as the result of
     the presence of such Third Party DNA Services on the Service.&nbsp; Any
     claim or dispute arising from or related to your purchase or use of Third
     Party DNA Services must be resolved between you and the applicable third
     party provider.</span></li>
  
<li class="MsoNormal"><span>ONCE YOU KNOW YOUR GENETIC INFORMATION, THE KNOWLEDGE IS
     IRREVERSIBLE. &nbsp; The information you receive may not be positive and
     may be upsetting to you or to others with whom you choose to share the
     information. &nbsp; If you elect to upload your Raw Data or do genetic
     testing and analysis, you do so at your own risk.</span></li>
  
<li class="MsoNormal"><span>Under no circumstances will CHONPS HEALTH TECH be responsible
     or liable for any injury (including emotional distress, mental anguish,
     bodily injury, and death) or loss arising from or related to your use of
     the Service or any information obtained through the Service (including any
     action or inaction by you based on such information), or your use of any
     Third Party DNA Services (including any genetic information you obtained
     from Third Party DNA Services), or your failure to consult with qualified
     independent experts or seek professional medical advice, diagnosis, or
     treatment
<b>.</b></span></li>
</ul>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>3. Genetic Counseling.</span></b></p>
<p class="MsoNormal"><span>Genetic testing and analysis may not be for
everyone. If you are unsure about whether or not to do genetic testing and
analysis, consult with your doctor, a genetic counselor, or other qualified
health care professional first so that you can make an informed decision. If,
after the testing and analysis, you need help with understanding or
interpretation of the results, or if you have questions regarding the results,
you should also consult with your doctor, a genetic counselor, or other
qualified health care professional.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>4. Eligibility.&nbsp;</span></b></p>
<p class="MsoNormal"><span>To be eligible to use the Service, you must
be&nbsp;
<i>at least 18 years of age</i>&nbsp;and have legal capacity to agree
to these Terms of Use, and your use of the Service must not violate any
applicable law or regulation in the jurisdiction in which you reside.</span></p>
<p class="MsoNormal">
<i><span>No one under the age of 18 is permitted
to use the Service.</span></i><span>&nbsp;However, parents and legal
guardians who are otherwise eligible to use the Service may use the Service to
obtain genetic information about their children under the age of 18.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>5. Privacy.&nbsp;</span></b></p>
<p class="MsoNormal"><span>CHONPS HEALTH TECH respects and values the
privacy of users of the Service. Please read our&nbsp;Privacy Policy&nbsp;for
information on our data collection, use, and sharing policies and practices in
connection with the Service.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>6. Compliance with Laws.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Your use of the Service is subject to
applicable laws and regulations and compliance with such applicable laws and
regulations is entirely your responsibility.</span></p>
<p class="MsoNormal"><span>The Service’s software and technology
components may be subject to U.S. export control laws and regulations. You
shall&nbsp;
<i>not</i>&nbsp;export, re-export, or transfer, directly or
indirectly, any of the Service’s software or technology components, or any U.S.
technical data acquired therefrom, or any products utilizing such data, in
violation of the U.S. export control laws or regulations.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>7. Reservation of Rights.&nbsp;</span></b></p>
<p class="MsoNormal"><span>We reserve the right to modify and
discontinue all or any part of the Service at any time in our sole discretion,
with or without notice to you. We will not be liable to you or to any other
user, if for any reason all or any part of the Service becomes unavailable at
any time or for any period. We also reserve the right to suspend or terminate
your account and your access to the Service, if we determine, in our sole
judgment, that you are in violation of these Terms of Use or any applicable law
or regulation, or that your use of the Service may expose CHONPS HEALTH TECH to
liability of any kind, or may adversely affect the reputation or goodwill of CHONPS
HEALTH TECH or the CHONPS Health Tech™ brand.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>8. Use of the Service.&nbsp;</span></b></p>
<p class="MsoNormal"><span>A main feature of the Service is genetic
traits analysis, which allow you to learn and discover personal (non-medical)
genetic traits (“
<b>Traits</b>”) about yourself and/or others (if you have
legal authority to obtain such information about them, or if they have given
you authorization to obtain such information about them) in multiple categories
including food/nutrition, sports/exercise, personality, physical
characteristics, and intelligence (the “
<b>Traits Analysis</b>”).</span></p>
<p class="MsoNormal"><span>In order to identify a person’s relevant
Traits, CHONPS HEALTH TECH needs to first collect information about that
person’s genotypes that is obtained through genetic testing (“
<b>Raw Data</b>”).
CHONPS HEALTH TECH collects Raw Data in one of two ways:</span></p>
<ol>
  
<li class="MsoNormal"><span>You can upload to the Service Raw Data obtained from a
     reputable third-party genetic testing source (23andMe, Ancestry.com, etc.)
     (“
<b>Third Party Source</b>”), which CHONPS HEALTH TECH can then analyze
     for the purpose of identifying relevant Traits; or</span></li>
  
<li class="MsoNormal"><span>You can provide us your login information (e.g., username and
     password) for a Third Party Source, which CHONPS HEALTH TECH can then use
     to access your Raw Data.&nbsp; If you choose to provide us your Raw Data
     through this method, you hereby authorize us to use your login information
     for the Third Party Source for the purpose of accessing your Raw Data.</span></li>
</ol>
<p class="MsoNormal"><span>The results of the Traits Analysis (i.e.,
individualized Traits information and reports) are viewable only through the
Service (by logging into a password-protected account).</span></p>
<p class="MsoNormal">
<b><span>8.1 Account Registration.&nbsp;</span></b></p>
<p class="MsoNormal"><span>In order for CHONPS HEALTH TECH to collect
Raw Data for the purpose of conducting the Traits Analysis, you must first
register an account on the Service, and registration is free. By registering an
account on the Service, you warrant that you are eligible to use the Service
pursuant to Section 4 of these Terms of Use and that all account information
you provide to us is your own information (or your child’s information) and is
truthful and accurate. You understand and agree that we may immediately suspend
or terminate your account if we have any reason to believe that you have
misrepresented or provided false account information to us. It is your
responsibility to keep your account information accurate and current. As the
account holder, you are responsible for safeguarding your account login
information (username and password), and you should notify us immediately in
the event your account login is lost, stolen, or used by another without your
permission. You are responsible for all activities on your account, including
activities by anyone whom you allow to access your account.</span></p>
<p class="MsoNormal">
<b><span>8.2 Informed Consent.&nbsp;</span></b></p>
<p class="MsoNormal"><span>In order for CHONPS HEALTH TECH to collect
Raw Data for the purpose of conducting the Traits Analysis, you must also
submit a properly completed and signed consent form (available at&nbsp;https://www.gene2h.com/informed-consent)
(the “
<b>Informed Consent</b>”) to CHONPS HEALTH TECH. In addition, CHONPS
HEALTH TECH may ask you to fill out a personal health and family history
questionnaire (the “
<b>Questionnaire</b>”), but this is optional and is not
required.</span></p>
<p class="MsoNormal">
<b><span>8.3 Raw Data.&nbsp;</span></b></p>
<p class="MsoNormal"><span>By uploading your Raw Data from a Third
Party Source to the Service, or by providing us your login information for a
Third Party Source to enable us to access your Raw Data, you expressly give
permission to CHONPS HEALTH TECH to perform genetic testing and Traits Analysis
on your DNA and you specifically request CHONPS HEALTH TECH to disclose the
testing and analysis results to you and to others you specifically authorize.</span></p>
<p class="MsoNormal"><span>If you let CHONPS HEALTH TECH collect and
analyze Raw Data about another person by uploading another person’s Raw Data to
the Service),&nbsp;or providing us another person’s login information for a
Third Party Source to enable us to access such person’s Raw Data,
<b>
<i>&nbsp;you
warrant that: (i) you either have legal authority to do so (e.g., if you are a
parent or legal guardian and are allowing CHONPS HEALTH TECH to collect and
analyze Raw Data about your child under the age of 18), or have obtained
express authorization from such person to allow CHONPS HEALTH TECH to collect
and analyze Raw Data about him/her; and (ii) you are not an insurance company
or an employer attempting to obtain information about an insured person or an
employee</i></b>. Also, if you let CHONPS HEALTH TECH collect and analyze Raw
Data about another person, you are deemed to be submitting the&nbsp;Informed
Consent&nbsp;(and the Questionnaire, which is optional) for and on behalf of
such person.</span></p>
<p class="MsoNormal"><span>If you upload Raw Data to the Service from
outside Hong Kong, or provide us your login information for a Third Party
Source to enable us to access your Raw Data, you warrant that doing so does not
violate any law or regulation in the country or jurisdiction in which you
reside, and you expressly authorize and consent to CHONPS HEALTH TECH
processing, testing, analyzing, using and storing such sample or Raw Data (as
the case may be) and all resulting genetic and Traits information, in Hong Kong.</span></p>
<p class="MsoNormal">
<b><span>8.4 Subscription.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Access to certain premium features of the
Service will require a monthly or annual subscription or à la carte purchase.
For example, a monthly subscription is required if you wish to unlock all
Traits available from CHONPS HEALTH TECH, plus any new Traits that CHONPS
HEALTH TECH may introduce from time to time.</span></p>
<p class="MsoNormal"><span>By making a subscription or à la carte
purchase from CHONPS HEALTH TECH, you warrant that you are the account holder
(or an authorized user) of the payment card that you use to pay for your
purchase, and that there are sufficient available funds on the card to cover
your purchase. We may immediately suspend or terminate your account if we have
any reason to believe that you have misrepresented or provided false payment
information to us.</span></p>
<p class="MsoNormal"><span>Prices and other terms for subscription and
à la carte purchases may change at any time. The price and terms in place when
you made your initial purchase or when your subscription last renewed will stay
in effect for the then-current period of your subscription, but new prices and
terms may apply to renewals or new subscription purchases. CHONPS HEALTH TECH
will give you advance notice before new prices or terms go into effect. If you
do not want to renew your subscription under the new price or terms, you may
cancel your subscription as described below.</span></p>
<p class="MsoNormal">
<b>
<i><span>NO REFUND; AUTOMATIC RENEWAL;
CANCELLATION</span></i><span>:</span></b><span>&nbsp;Unless
expressly otherwise specified by CHONPS HEALTH TECH, all subscription and à la
carte purchases made on the Service are&nbsp;
<b>
<i>FINAL AND NON-REFUNDABLE</i></b>.
A monthly subscription is subject to automatic billing and renewal, unless you
cancel the subscription&nbsp;
<b>
<i>no later than two (2) business days before
the next scheduled billing/renewal date</i></b>. To cancel, please log into
your account on the Service and then go to the tab “
<b>PLANS</b>” and follow
the instructions. Timely cancellation will stop automatic billing/renewal and
will take effect immediately (usually on the same day).&nbsp;
<b>
<i>This means
that, on the day of your cancellation, your account on the Service will be
deactivated, and you will no longer have access to any area of the Service that
requires an active account.</i></b>&nbsp;To illustrate, if you purchase a
monthly subscription on May 25, 2019, your subscription will automatically
renew on June 25, 2019, unless you cancel no later than June 20, 2019 (which is
two business days before June 25). Suppose that you cancel your subscription on
June 15, 2019. In such case, cancellation will take effect on June 15, 2019,
and your account will be deactivated on that day, upon which you will lose
access to any area of the Service that requires an active account. On the other
hand, if you don’t cancel by June 20, 2019, then your subscription will automatically
renew (and your payment card will automatically be charged) on June 25, 2019
for another 30 days.</span></p>
<p class="MsoNormal"><span>You must review and agree to our&nbsp;Auto-Renewal
Terms&nbsp;prior to signing up for any subscription service.&nbsp;</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>9. Ownership; Grant of Licenses.</span></b></p>
<p class="MsoNormal">
<b><span>9.1 Our Ownership of the Service.&nbsp;</span></b></p>
<p class="MsoNormal"><span>You expressly acknowledge and agree
that,&nbsp;
<i>other than User Data&nbsp;</i>(as defined in Section 9.3 below), CHONPS
HEALTH TECH and its affiliates, licensors and partners and their respective
successors and assigns (collectively, “
<b>CHONPS HEALTH TECH and Related
Parties</b>”) retain sole and exclusive ownership of all worldwide right, title
and interest, including all copyrights, patent rights, trade secret rights, and
other intellectual property and proprietary rights, in and to the Service,
including all content, data, information, reports, software, tools, links and
resources comprised in the Service or provided through the Service, as well as
all technologies used by CHONPS HEALTH TECH to provide and operate the Service.
Other than a limited license to use as provided in Section 9.2 below, you have
and acquire no other right or license with respect to the Service or any
portion or component thereof. Unless expressly authorized by applicable law or
in writing by CHONPS HEALTH TECH, you may not copy, reproduce, publicly perform
or display, transmit, modify or otherwise create derivative works from, sell,
distribute, or otherwise make unauthorized use of the Service or any portion or
component thereof. Any unauthorized use of the Service or any portion or
component thereof is strictly prohibited and may result in civil and/or
criminal penalties. CHONPS HEALTH TECH and Related Parties reserve all rights
not expressly granted herein. There are no implied rights or licenses granted
to you under these Terms of Use.</span></p>
<p class="MsoNormal"><span>The CHONPS Health Tech™ name and logo and
all other marks, logos, and other business identifiers of CHONPS HEALTH TECH
are registered or unregistered trademarks of CHONPS HEALTH TECH (collectively,
“
<b>Company Trademarks</b>”). Any unauthorized use of our Company Trademarks is
strictly prohibited and may result in civil and/or criminal penalties.</span></p>
<p class="MsoNormal"><span>Third-party marks and logos appearing on
the Service are the property of their respective owners.</span></p>
<p class="MsoNormal">
<b><span>9.2 Our License to You; Conditions of
Use.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Subject to your compliance with these Terms
of Use and all applicable laws and regulations, CHONPS HEALTH TECH grants you a
revocable, non-exclusive, non-transferable, non-sublicensable, limited personal
license to access the Service&nbsp;
<b>
<i>for your lawful personal and noncommercial
uses only</i></b>.</span></p>
<p class="MsoNormal"><span>For any individualized Traits information
or reports (in any format or medium) you lawfully obtain from the Service, the
foregoing license allows you to keep such information or reports for lawful
personal and noncommercial uses only, and&nbsp;
<b>
<i>NOT for publication,
distribution, sale or transfer to others</i></b>&nbsp;(except that you may
share such information or reports with family members, friends, and health care
professionals, as long as it is for lawful personal and noncommercial uses
only). Unless expressly authorized by applicable law or in writing by CHONPS
HEALTH TECH, you may not copy, reproduce, publicly perform or display,
transmit, modify or otherwise create derivative works from, sell, distribute,
or otherwise make unauthorized use of any individualized Traits information or
reports obtained from the Service.</span></p>
<p class="MsoNormal"><span>As a condition to your use of the Service,
you expressly agree&nbsp;
<b>
<i>not</i></b>&nbsp;to:</span></p>
<ul>
  
<li class="MsoNormal"><span>use the Service in violation of these Terms of Use or any
     applicable law or regulation;</span></li>
  
<li class="MsoNormal"><span>use the Service for any unauthorized, fraudulent, or malicious
     purpose;</span></li>
  
<li class="MsoNormal"><span>use the Service in violation of any privacy, property, or other
     right of another person, including, without limitation: impersonating
     another person on the Service, or when you have no legal authority or
     valid authorization to do so, (i) registering an account on the Service in
     the name of another person, (ii) uploading another person’s Raw Data to
     the Service, or (iii) providing us another person’s login information for
     a Third Party Source to enable us to access such person’s Raw Data;</span></li>
  
<li class="MsoNormal"><span>use the Service for any business or commercial purpose;</span></li>
  
<li class="MsoNormal"><span>use the Service in any manner that, in our sole judgment, could
     damage, disable, overburden, impair or interfere with others’ use of the
     Service;</span></li>
  
<li class="MsoNormal"><span>reverse engineer, decompile, disassemble, or otherwise attempt
     to derive any source code or algorithm associated with the Service;</span></li>
  
<li class="MsoNormal"><span>use any robot, spider, or other automatic device, program,
     process, or means to access the Service, including for monitoring or
     copying any content or information from the Service;</span></li>
  
<li class="MsoNormal"><span>access or attempt to access any Service system, server,
     hardware, software, account, content, report, data, or information that
     you are not authorized to access; and</span></li>
  
<li class="MsoNormal"><span>upload, post, or otherwise transmit any material that contains
     software viruses or any other computer code, files, or programs designed
     to interrupt, destroy, or limit the functionality of any computer software
     or hardware or telecommunications equipment;</span></li>
  
<li class="MsoNormal"><span>engage in framing, mirroring, or otherwise simulating the
     appearance or function of the Service;</span></li>
  
<li class="MsoNormal"><span>use the Service from a foreign country that is subject to a
     U.S. Government embargo, or that has been designated by the U.S.
     Government as a “terrorist-supporting” country. &nbsp;</span></li>
</ul>
<p class="MsoNormal"><span>You further expressly acknowledge and agree
that your use of any software comprised in the Service, including any
downloadable software application you install on a computer or mobile device,
is subject to the following additional conditions:</span></p>
<ul>
  
<li class="MsoNormal"><span>Any such software is licensed, and&nbsp;
<i>not</i>&nbsp;sold or
     transferred, to you.</span></li>
  
<li class="MsoNormal"><span>You may not redistribute, sell, offer to sell, lend, rent,
     lease, transfer, or otherwise furnish any such software to a third party.</span></li>
  
<li class="MsoNormal"><span>You may not modify, translate, or otherwise make derivative
     works from, or reverse engineer, decompile, disassemble, or otherwise
     attempt to derive the source code of, any such software.</span></li>
  
<li class="MsoNormal"><span>You may not bypass, disable, deactivate, or render ineffective
     (or attempt to do so) any security mechanism or firewall associated with
     any such software.</span></li>
  
<li class="MsoNormal"><span>You may not download, install, use, export, or re-export any
     such software or any underlying information or technology except in full
     compliance with U.S. export control laws and regulations.</span></li>
  
<li class="MsoNormal"><span>From time to time we may make software updates to the Service,
     and you understand that it may be necessary for you to download and
     install such updates in order for the Service to work properly on your
     computer or mobile device.</span></li>
</ul>
<p class="MsoNormal">
<b><span>9.3 User Data.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Subject to the license granted by you to CHONPS
HEALTH TECH and Related Parties as provided below, you retain ownership of all
“
<b>User Data</b>,” which means and includes the following:</span></p>
<ul>
  
<li class="MsoNormal"><span>“
<b>Account Information</b>,” which refers to personal
     information (including, without limitation, name, email address, mailing
     address, phone number, date of birth, and payment card information) you
     provide to us when registering an account on the Service or making a
     purchase from us;</span></li>
  
<li class="MsoNormal"><span>“
<b>Self-Reported Information</b>,” which refers to personal
     health and family history information you provide to us voluntarily (such
     as by completing the optional Questionnaire described in Section 8.2
     above); and</span></li>
  
<li class="MsoNormal"><span>“
<b>Genetic Information</b>,” which refers to all Raw Data you
     let CHONPS HEALTH TECH collect for conducting the Traits Analysis and all
     personal Traits information provided to you by CHONPS HEALTH TECH
     resulting from the Traits Analysis;&nbsp;
<b>
<i>provided, however, that you
     expressly acknowledge and agree that CHONPS HEALTH TECH owns and retains
     copyrights and other intellectual property rights in and to all
     protectable elements contained in the results of the Traits Analysis,
     including text, graphics, images, tables, charts, diagrams, notes,
     commentaries, and other original content contained therein, as well as the
     original selection, arrangement, and organization of the individualized
     Traits information</i></b>.</span></li>
</ul>
<p class="MsoNormal"><span>With respect to User Data, you expressly
acknowledge and agree as follows:</span></p>
<ul>
  
<li class="MsoNormal"><span>Your&nbsp;
<i>Account Information</i>&nbsp;will be used and
     shared as disclosed in our&nbsp;Privacy Policy.</span></li>
  
<li class="MsoNormal"><span>By accessing the Traits Analysis feature of the Service, you
     expressly grant to CHONPS HEALTH TECH and Related Parties a worldwide,
     non-exclusive, royalty-free, fully paid up, sublicensable and transferable
     license to collect, store, process, test, analyze, compare, index, use,
     reproduce, and otherwise exploit your&nbsp;
<i>Self-Reported Information</i>&nbsp;and&nbsp;
<i>Genetic
     Information&nbsp;</i>(whether such information pertains to you or another
     person) for any and all lawful purposes including, without limitation: (i)
     operating and providing the Service; (ii) making improvements and
     modifications to the Service; (iii) developing new genetic information
     products and services; (iv) conducting research in the fields of genomics
     and genetics; and (v) combining your and other users’&nbsp;
<i>Self-Reported
     Information</i>&nbsp;and&nbsp;
<i>Genetic Information</i>&nbsp;to compile
     and generate&nbsp;
<i>aggregated and anonymized</i>&nbsp;
<i>data about
     users of the Service&nbsp;</i>(no individual user will be identified or
     reasonably identifiable in such data) (“
<b>Aggregated and Anonymized Data</b>”),
     and publishing, distributing, selling, licensing, and otherwise exploiting
     such data.</span></li>
  
<li class="MsoNormal"><span>We will delete your User Data: (i) as provided in our&nbsp;Privacy
     Policy; (ii) upon receipt of a written request from you (however, we
     reserve the right to verify your identity before acting on your request);
     (iii) upon deactivation of your account; (iv) if required to do so
     pursuant to applicable law or a valid court or government order; or (v) when
     we determine (in our sole discretion) that it is advisable to do so.</span></li>
  
<li class="MsoNormal"><span>All Aggregated and Anonymized Data will belong to CHONPS HEALTH
     TECH and Related Parties and may be used, exploited, and retained&nbsp;
<i>indefinitely</i>&nbsp;by
     CHONPS HEALTH TECH and Related Parties.</span></li>
  
<li class="MsoNormal">
<b><span>Unless otherwise provided in a separate written agreement
     entered into by you and CHONPS HEALTH TECH, you will not receive any
     compensation, credit, or attribution, and you expressly waive any and all
     rights and claims to compensation, credit, and attribution, with respect
     to any research conducted, any new product or service developed, or any
     improvement to the Service made by CHONPS HEALTH TECH and Related Parties
     utilizing your Self-Reported Information and Genetic Information.</span></b><span></span></li>
</ul>
<p class="MsoNormal">
<b><span>9.4 User Feedback.&nbsp;</span></b></p>
<p class="MsoNormal"><span>If you submit to CHONPS HEALTH TECH any
ideas, stories, comments, reviews, testimonials, suggestions, or other feedback
(whether solicited or unsolicited) regarding the Service (collectively, “
<b>Feedback</b>”),
you expressly acknowledge and agree that: (i) CHONPS HEALTH TECH and Related
Parties will be free to copy, use, publish, adapt, and otherwise exploit your
Feedback in perpetuity and throughout the world for any and all business
purposes, including, without limitation, for publicity, advertising and
promotion, product and service improvement, and development of new products and
services; (ii) your Feedback submission is voluntary and consensual and is made
without any condition or reservation of rights, including, without limitation,
any condition of compensation, payment, credit, attribution, secrecy, or
confidentiality; (iii) your Feedback submission does not give rise to any
contractual, fiduciary, or confidential relationship of any kind (whether
express or implied) between you and CHONPS HEALTH TECH; and (iv) your Feedback
may be used and retained indefinitely by CHONPS HEALTH TECH and Related
Parties.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>10. Disclaimer of Warranties;
Limitations of Liability.&nbsp;</span></b></p>
<p class="MsoNormal"><span>You expressly acknowledge and agree as
follows:</span></p>
<ul>
  
<li class="MsoNormal"><span>THE SERVICE AND ALL INFORMATION PROVIDED THROUGH THE SERVICE
     ARE PROVIDED “AS IS” AND “AS AVAILABLE” WITH ALL FAULTS AND WITHOUT
     WARRANTIES OF ANY KIND, WHETHER EXPRESS OR IMPLIED. &nbsp;TO THE FULLEST
     EXTENT PERMITTED BY APPLICABLE LAW, CHONPS HEALTH TECH AND RELATED PARTIES
     DISCLAIM ALL WARRANTIES, EXPRESS OR IMPLIED, WITH RESPECT TO THE SERVICE
     AND ANY INFORMATION PROVIDED THROUGH THE SERVICE, INCLUDING, WITHOUT
     LIMITATION, IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A
     PARTICULAR PURPOSE, AND WARRANTIES OF TITLE AND NON-INFRINGEMENT OF
     PROPRIETARY RIGHTS. &nbsp;WITHOUT LIMITING THE GENERALITY OF THE
     FOREGOING, CHONPS HEALTH TECH AND RELATED PARTIES DO NOT WARRANT THAT: (i)
     THE SERVICE WILL BE RELIABLE OR USEFUL, OR WILL MEET YOUR EXPECTATIONS;
     (ii) THE SERVICE WILL BE ERROR-FREE, OR ANY DEFECTS OR ERROR IN THE
     SERVICE WILL BE CORRECTED; (iii) THE SERVICE WILL BE UNINTERRUPTED OR WILL
     BE AVAILABLE AT ANY PARTICULAR TIME OR LOCATION; OR (iv) THE SERVICE WILL
     BE SECURE AND FREE OF VIRUSES OR OTHER HARMFUL COMPONENTS.</span></li>
  
<li class="MsoNormal"><span>TO THE FULLEST EXTENT PERMITTED BY APPLICABLE LAW, IN NO EVENT
     WILL CHONPS HEALTH TECH AND RELATED PARTIES BE LIABLE TO YOU OR ANY OTHER
     USER (WHETHER UNDER CONTRACT, TORT, NEGLIGENCE, STRICT LIABILITY, WARRANTY
     OR ANY OTHER LEGAL OR EQUITABLE THEORY) FOR ANY INDIRECT, SPECIAL,
     INCIDENTAL, CONSEQUENTIAL, OR PUNITIVE DAMAGES (INCLUDING, WITHOUT LIMITATION,
     PERSONAL INJURY, PAIN AND SUFFERING, EMOTIONAL DISTRESS, MENTAL ANGUISH,
     LOSS OF USE, AND LOSS OF DATA) ARISING OUT OF OR RELATED TO (i) THE
     SERVICE OR ANY INFORMATION PROVIDED THROUGH THE SERVICE OR (ii) YOUR USE
     OF (OR INABILITY TO USE) OR YOUR RELIANCE ON THE SERVICE OR ANY
     INFORMATION PROVIDED THROUGH THE SERVICE, EVEN IF CHONPS HEALTH TECH AND
     RELATED PARTIES HAVE BEEN ADVISED OF THE POSSIBILITY OF SUCH LOSS OR
     DAMAGES.</span></li>
  
<li class="MsoNormal"><span>TO THE FULLEST EXTENT PERMITTED BY APPLICABLE LAW, IN NO EVENT
     WILL CHONPS HEALTH TECH AND RELATED PARTIES BE LIABLE TO YOU FOR ANY
     DAMAGES ARISING OUT OF OR RELATED TO (i) THE SERVICE OR ANY INFORMATION
     PROVIDED THROUGH THE SERVICE OR (ii) YOUR USE OF (OR INABILITY TO USE) OR
     YOUR RELIANCE ON THE SERVICE OR ANY INFORMATION PROVIDED THROUGH THE SERVICE,
     IN A TOTAL AMOUNT THAT EXCEEDS THE SUBSCRIPTION FEES ACTUALLY PAID BY YOU
     TO CHONPS HEALTH TECH DURING THE THREE (3) MONTHS IMMEDIATELY PRECEDING
     THE OCCURRENCE FOR WHICH DAMAGES ARE CLAIMED, OR FIFTY U.S. DOLLARS
     (US$50.00), WHICHEVER IS GREATER.</span></li>
</ul>
<p class="MsoNormal"><span>BECAUSE SOME JURISDICTIONS DO NOT ALLOW THE
EXCLUSION OR LIMITATION OF CERTAIN WARRANTIES, DAMAGES, OR LIABILITIES, SOME OF
THE EXCLUSIONS AND LIMITATIONS SET FORTH ABOVE MAY NOT APPLY TO YOU. NOTHING IN
THIS SECTION 10 AFFECTS ANY CONSUMER RIGHT OR REMEDY THAT CANNOT BE EXCLUDED OR
LIMITED UNDER APPLICABLE LAW.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>11. Indemnification; Hold Harmless.&nbsp;</span></b></p>
<p class="MsoNormal"><span>You agree to indemnify and hold harmless CHONPS
HEALTH TECH and Related Parties and their respective shareholders, investors,
members, officers, directors, employees, agents, representatives, advisors, and
contractors from and against any and all third-party claims, losses, damages,
liabilities, costs, and expenses (including reasonable attorney’s fees) arising
out of or relating to: (i) your use or misuse of the Service or any third party
product or service; (ii) any Raw Data uploaded by you or accessed by us; (iii)
your violation of these Term of Use or any applicable law or regulation; (iv)
your violation of any intellectual property, privacy, contractual, or other
right of any other person or entity; or (v) any agreement or purchase
transaction you enter into with a third party product or service provider. CHONPS
HEALTH TECH reserves the right, at our own expense, to assume the exclusive
defense and settlement of any claim for which you are required to indemnify us
and you agree to cooperate with our defense and settlement of such claim.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>12. Arbitration.</span></b></p>
<p class="MsoNormal">
<b><span>12.1 Agreement to Arbitrate.&nbsp;</span></b></p>
<p class="MsoNormal"><span>This Section 12 is referred to herein as
the “
<b>Arbitration Agreement</b>.” The United States Federal Arbitration Act (
<i>9
U.S.C. §§ 1-16</i>) governs the interpretation and enforcement of this Arbitration
Agreement.</span></p>
<p class="MsoNormal"><span>You and CHONPS HEALTH TECH agree that any
and all controversies, claims, and disputes arising out of or related to these
Terms of Use or the Service or any information provided through the Service,
whether based in contract, tort, warranty, statute, or any other legal or
equitable basis, including, without limitation, any dispute or claim relating
to the formation, interpretation, or enforceability of any part of these Terms
of Use (including the scope and enforceability of this Arbitration Agreement)
and any claim that all or any part of these Terms of Use is void or voidable
(collectively, “
<b>Claims</b>” and individually, a “
<b>Claim</b>”),&nbsp;
<b>
<i>shall
be finally resolved by binding arbitration, rather than in court</i></b>;
except that you and we each retain the right: (i) to bring an individual action
in small claims court (if the Claim in question qualifies for small claims
court); and (ii) to seek injunctive or other equitable relief in court against
actual or threatened infringement, misappropriation, or violation of intellectual
property rights.</span></p>
<p class="MsoNormal"><span>There is no judge or jury in arbitration,
and court review of an arbitration award is limited. However, an arbitrator can
award on an individual basis the same damages and relief as a court.</span></p>
<p class="MsoNormal">
<b><span>12.2&nbsp;
<i>CLASS ACTION WAIVER</i>.&nbsp;</span></b></p>
<p class="MsoNormal"><span>YOU AND CHONPS HEALTH TECH AGREE THAT EACH
PARTY MAY BRING CLAIMS AGAINST THE OTHER ONLY ON AN INDIVIDUAL BASIS AND NOT AS
A PLAINTIFF OR CLASS MEMBER IN ANY PURPORTED CLASS OR REPRESENTATIVE ACTION OR
PROCEEDING. UNLESS BOTH YOU AND CHONPS HEALTH TECH AGREE OTHERWISE, THE
ARBITRATOR MAY NOT CONSOLIDATE OR JOIN MORE THAN ONE PERSON'S OR PARTY'S CLAIMS
AND MAY NOT OTHERWISE PRESIDE OVER ANY FORM OF A CONSOLIDATED, REPRESENTATIVE,
OR CLASS PROCEEDING. ALSO, THE ARBITRATOR MAY AWARD RELIEF (INCLUDING MONETARY,
INJUNCTIVE, AND DECLARATORY RELIEF) ONLY IN FAVOR OF THE INDIVIDUAL PARTY
SEEKING RELIEF AND ONLY TO THE EXTENT NECESSARY TO PROVIDE RELIEF NECESSITATED
BY THAT PARTY'S INDIVIDUAL CLAIM(S).</span></p>
<p class="MsoNormal">
<b><span>12.3 Procedures.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Arbitration will be conducted by a single
and neutral arbitrator in accordance with the American Arbitration
Association's ("
<b>AAA</b>") Consumer Arbitration Rules and
procedures (the "
<b>AAA Rules</b>"), as modified by this Arbitration
Agreement. If there is any inconsistency between the AAA Rules and this
Arbitration Agreement, the terms of this Arbitration Agreement will control
unless the arbitrator determines that the application of the inconsistent
Arbitration Agreement terms would not result in a fundamentally fair
arbitration. To learn more about arbitration through the AAA, visit&nbsp;http://www.adr.org.
The AAA Rules are available at&nbsp;https://www.adr.org/sites/default/files/Consumer_Rules_Web_0.pdf&nbsp;or
by calling the AAA at 1-800-778-7879.</span></p>
<p class="MsoNormal"><span>Prior to initiating arbitration, you and we
agree to first make reasonable efforts to try to resolve a Claim amicably
through good-faith negotiations. If a Claim cannot be resolved amicably within
60 days after a party gives written notice (email sufficient) of the Claim to
the other, then either party may initiate arbitration in accordance with this
Arbitration Agreement.</span></p>
<p class="MsoNormal"><span>To initiate arbitration, a party must
provide the other party with a written Demand for Arbitration as specified in
the AAA Rules (form available at&nbsp;https://www.adr.org/sites/default/files/document_repository/Consumer_Demand_for_Arbitration_Form_1.pdf).
If you initiate arbitration, please send your written Demand for Arbitration
to:</span></p>
<p class="MsoNormal"><span>CHONPS Health Tech, Inc.<br /> Attn.: Legal / Arbitration<br /> 
2150 Shattuck Avenue<br /> 
Berkeley, CA, 94704<br /> 
Email: support@gene2h.com</span></p>
<p class="MsoNormal"><span>If we initiate arbitration, we will send
our written Demand for Arbitration to you at the email or mailing address you
have provided to us.</span></p>
<p class="MsoNormal"><span>In arbitration, the arbitrator will: (i)
follow these Terms of Use and apply internal laws of Hong Kong, consistent with
the United States Federal Arbitration Act and applicable statutes of
limitations (or, to the extent (if any) that federal law prevails, will apply
the applicable federal laws of the United States, irrespective of any conflict
of law principles); (ii) entertain any motion to dismiss, motion to strike,
motion for judgment on the pleadings, motion for complete or partial summary
judgment, motion for summary adjudication, or any other dispositive motion
consistent with California or federal rules of procedure, as applicable; (iii)
honor claims of privilege recognized at law; and (iv) have authority to award
any form of legal or equitable relief consistent with applicable laws (except
that the arbitrator may not award any punitive, incidental, indirect, special,
or consequential damages).&nbsp;
<b>
<i>The decision of the arbitrator will be
final and binding on both parties</i>.</b>&nbsp;Judgment on the arbitration
award rendered may be entered in any court of competent jurisdiction.</span></p>
<p class="MsoNormal">
<b><span>12.4 Venue.&nbsp;</span></b></p>
<p class="MsoNormal"><span>The arbitration shall be held in the county
in which you reside or at another mutually agreed location. If the value of the
relief sought is $10,000 or less, you or CHONPS HEALTH TECH may elect to have
the arbitration conducted by telephone or based solely on written submissions,
which election shall be binding on each party, but subject to the arbitrator's
discretion to require an in-person hearing if the circumstances warrant.
Attendance at any in-person hearing may be made by telephone by either or both
parties unless the arbitrator requires otherwise.</span></p>
<p class="MsoNormal">
<b><span>12.5 Confidentiality.&nbsp;</span></b></p>
<p class="MsoNormal"><span>You and CHONPS HEALTH TECH agree that the
entire arbitration proceeding will be conducted in a confidential manner and
that the arbitrator’s decision and award will be kept confidential by both
parties and, except as may be required by applicable law or a valid court
order, will not be disclosed to any third party without the express prior
written consent of both parties.</span></p>
<p class="MsoNormal">
<b><span>12.6 Costs of Arbitration.&nbsp;</span></b></p>
<p class="MsoNormal"><span>Payment of all filing, administration, and
arbitrator fees (collectively, the "
<b>Arbitration Fees</b>") will be
governed by the AAA Rules. Each party will be responsible for all other fees it
incurs in connection with the arbitration, including without limitation, all
attorney fees.</span></p>
<p class="MsoNormal">
<b><span>12.7 Severability.&nbsp;</span></b></p>
<p class="MsoNormal"><span>If a court decides that any term or
provision of this Arbitration Agreement other than Section 12.2 is invalid or
unenforceable, the parties agree to replace such term or provision with a term
or provision that is valid and enforceable and that comes closest to expressing
the intention of the invalid or unenforceable term or provision, and this
Arbitration Agreement shall be enforceable as so modified.</span></p>
<p class="MsoNormal"><span>If a court decides that any of the
provisions of Section 12.2 is invalid or unenforceable, then the entirety of
this Arbitration Agreement shall be null and void. The remainder of these Terms
of Use will continue to apply.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>13. Governing Law; Jurisdiction.&nbsp;</span></b></p>
<p class="MsoNormal"><span>These Terms of Use shall be governed by and
construed in accordance with the laws of Hong Kong (without regard to the
conflict of laws provisions thereof),&nbsp;
<i>except</i>&nbsp;that the Hong
Kong shall govern the interpretation and enforcement of the Arbitration
Agreement contained in Section 12 above. The United Nations Convention on
Contracts for the International Sale of Goods shall not apply to these Terms of
Use.</span></p>
<p class="MsoNormal"><span>With respect to any Claim (as defined in
Section 12.1 above) that is not subject to arbitration under Section 12 above,
or in the event the arbitration agreement set forth in Section 12 above is
found to be void or unenforceable: (i) you and we each agree to submit to the
exclusive jurisdiction of the courts located in Hong Kong to resolve any
non-arbitrable Claim; and (ii) you agree to waive all defenses of lack of
personal jurisdiction, venue and/or forum non conveniens with respect to venue
and jurisdiction in the aforementioned courts.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>14. Limitation on Time to File Claims.&nbsp;</span></b></p>
<p class="MsoNormal"><span>YOU AGREE THAT ANY CAUSE OF ACTION OR CLAIM
YOU MAY HAVE AGAINST CHONPS HEALTH TECH ARISING OUT OF OR RELATED TO THESE
TERMS OF USE OR THE SERVICE OR ANY INFORMATION PROVIDED THROUGH THE SERVICE,
MUST BE BROUGHT&nbsp;
<b>
<i>WITHIN ONE (1) YEAR</i></b>&nbsp;AFTER THE CAUSE OF
ACTION OR CLAIM ACCRUES, OR BE PERMANENTLY BARRED.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>15. Changes.&nbsp;</span></b></p>
<p class="MsoNormal"><span>From time to time, we may modify these
Terms of Use to accommodate new technology, industry practices, regulatory
requirements, or for other purposes. If we make a material change to the TOS,
we will provide you with notice thirty (30) days prior to the effective date of
the change by posting a notice on our website or sending a message to the email
address associated with your account. Unless you notify us within thirty (30)
days from the time you receive notice of the new terms that you do not agree to
the terms, you will be deemed to have agreed to the new TOS. If any change to
the TOS is unacceptable to you, you may stop using our Services and delete your
account at any time. You acknowledge and agree that if you use the Services
after the date on which the TOS have changed, 23andMe will treat your use as acceptance
of the updated TOS.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>16. Electronic Communications.&nbsp;</span></b></p>
<p class="MsoNormal"><span>When you communicate with the Company
through the Service or send us email, you are communicating with us
electronically. You hereby: (a) consent to receive communications from Company
in an electronic form; and (b) agree that all terms and conditions, agreements,
notices, disclosures, and other communications that we provide to you
electronically satisfy any legal requirement that such communications be in
writing. The foregoing does not affect any rights you may have which cannot be
waived under applicable law.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>17. Miscellaneous.&nbsp;</span></b></p>
<p class="MsoNormal"><span>These Terms of Use (together with our&nbsp;Privacy
Policy, the&nbsp;Informed Consent&nbsp;submitted by you, and any other legal
notices referenced herein) constitute the entire agreement between you and CHONPS
HEALTH TECH concerning the Service. If any provision of these Terms of Use is
deemed invalid by a court of competent jurisdiction, the invalidity of such
provision shall not affect the validity of the remaining provisions of these
Terms of Use, all of which shall remain in full force and effect. No waiver of
any provision of these Terms of Use shall be deemed a further or continuing
waiver of such provision or a waiver of any other provision, and our failure to
assert any right or provision under these Terms of Use shall not constitute a
waiver of such right or provision. The provisions of Sections 2, 8, 9, 10, 11,
12, 13, 14, 15, 16 and 17 of these Terms of Use shall survive any termination
of these Terms of Use.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>18. Contact Information.&nbsp;</span></b></p>
<p class="MsoNormal"><span>The Service is provided by CHONPS HEALTH
TECH, Inc. If you have any questions, complaints, or claims with respect to the
Service, you may contact us at&nbsp;support@gene2h.com.</span></p>
<p class="MsoNormal"><span>CHONPS HEALTH TECH, Inc. is located at 1F, 5
Sassoon Road, Pokfulam, Hong Kong.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span></span></p>]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=16&amp;l=tw</link>
      <category>16</category>
      <pubDate>2022-01-17 02:52:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Informed Consent for Raw Data Upload and Analysis 數據上傳分析知情衕意書</title>
      <description><![CDATA[  <p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>Informed Consent for Raw Data Upload and
Analysis</span></b></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span>Please review this form and, if you agree,
provide your consent for genetic testing at the bottom of the form. If you do
not agree, please do not submit any samples, Raw Data, or other information or
materials to CHONPS Health Tech, Inc. (“CHONPS HEALTH TECH”) or our third-party
partners in connection with the CHONPS HEALTH TECH CHONPS Health Tech service.</span></p>
<p class="MsoNormal"><span>One of our missions at CHONPS HEALTH TECH
is to help our customers understand how their DNA may impact certain personal
traits. This Informed Consent for Raw Data Upload (“Informed Consent”) explains:</span></p>
<ul>
  
<li class="MsoNormal"><span>What CHONPS Health Tech is and how it works</span></li>
  
<li class="MsoNormal"><span>What results you will get and who can see them</span></li>
  
<li class="MsoNormal"><span>The potential benefits, potential risks and limitations of
     using CHONPS Health Tech</span></li>
  
<li class="MsoNormal"><span>How to withdraw your consent</span></li>
  
<li class="MsoNormal"><span>Who to contact if you have questions</span></li>
</ul>
<p class="MsoNormal"><span>Please review this Informed Consent
carefully. If you agree to allow CHONPS HEALTH TECH to access and use your data
to perform the CHONPS Health Tech service as described herein click the “I
consent” prompt at the end of this document. You must be 18 years or older to
use CHONPS Health Tech.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Key Terms</span></b></p>
<ul>
  
<li class="MsoNormal">
<b><span>CHONPS HEALTH TECH:&nbsp;</span></b><span>This is
     us, CHONPS HEALTH TECH, Inc. We will refer to CHONPS HEALTH TECH as “we”,
     “us” and “our” throughout this Informed Consent.</span></li>
  
<li class="MsoNormal">
<b><span>CHONPS Health Tech</span></b><span>: Our
     non-medical, personal genetic information analysis service.</span></li>
  
<li class="MsoNormal">
<b><span>Personal Information</span></b><span>: Information
     that can be used to identify you, either alone or in combination with
     other information.</span></li>
  
<li class="MsoNormal">
<b><span>Raw Data:&nbsp;</span></b><span>Information about
     your genotypes that is generated through the processing of your saliva or
     blood by Third Party DNA Services. Your Raw Data contains the “letters”
     (nucleotides A, C, G, T) that comprise DNA.</span></li>
  
<li class="MsoNormal">
<b><span>Self-Reported Information:&nbsp;</span></b><span>Information
     you provide about yourself that is not part of your DNA or derived from
     your Raw Data. Self-Reported Information may include details about your
     health, family tree, behaviors, and lifestyle.</span></li>
  
<li class="MsoNormal">
<b><span>Third Party DNA Services:&nbsp;</span></b><span>Companies
     and organizations not related to or operated by us that you may use to
     obtain DNA testing and results.</span></li>
  
<li class="MsoNormal">
<b><span>Traits</span></b><span>: The characteristics or
     attributes that may be influenced by your DNA. Your Traits may include
     your preferences, characteristics, psychological trends, preferences,
     predispositions, behavior, attitudes, intelligence, abilities, and
     aptitudes. The traits we analyze as part of the service are personal - not
     medical - in nature.</span></li>
</ul>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>What is CHONPS Health Tech?</span></b></p>
<p class="MsoNormal"><span>Every individual is made up of trillions of
cells. Cells can be thought of as small, microscopic packets containing our
DNA. DNA is necessary for the normal health and maintenance of our body. It is
particularly important because it allows one’s genetic information, which
influences health and physical characteristics, to be passed down from one
generation to the next.</span></p>
<p class="MsoNormal"><span>Genes are segments of coding and non-coding
DNA that provide instructions for the formation of proteins and other important
biological compounds. Changes found in an individual’s genes or DNA (as
compared to a normal, healthy individual) can cause disease or increase one’s
risk for disease. Conversely, gene changes may also be protective against
certain illnesses and diseases.</span></p>
<p class="MsoNormal"><span>We created CHONPS Health Tech to give you
insights about your DNA. We want to empower you by giving you information about
how your DNA shapes your nutrition, fitness, personality and intelligence
Traits.</span></p>
<p class="MsoNormal"><span>CHONPS Health Tech provides Trait analysis
for healthy individuals. CHONPS Health Tech is not a diagnostic test and should
not be used to diagnose any disease in yourself or others, is not appropriate
for use the cure, mitigation, treatment or prevention of disease, and is not
intended for the assessment of a health condition. If you have concerns about a
disease or medical condition, you should discuss your concerns with your
healthcare provider.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>How does CHONPS Health Tech work?</span></b></p>
<p class="MsoNormal"><span>To use CHONPS Health Tech, you must first
create a CHONPS Health Tech account and then upload your Raw Data. The Raw Data
you upload should come from one of the following Third Party DNA Services:
23andMe, My Heritage, or Ancestry.com. We may expand the list of Third Party
DNA Services in the future. Before uploading your Raw Data, or the Raw Data
about another person, and by signing this Informed Consent, you confirm that
you have the rights and permissions necessary to share that Raw Data with us
for use and disclosure as described in this Informed Consent.</span></p>
<p class="MsoNormal"><span>Once we receive your Raw Data, we and our
scientists analyze it to identify variants in the sequencing that may indicate
the presence of, or risk for, a variety of non-medical Traits, such as your
cognitive ability, height, waist size, and muscular strength. Variations can
occur in the coding and/or non-coding portions of your DNA. We look at both the
coding and non-coding portions to better predict your Traits.</span></p>
<p class="MsoNormal"><span>In addition to uploading your Raw Data, you
may also choose to provide us with certain other Self-Reported Information that
will [help us improve your Trait analysis and reports]. First, you may complete
a questionnaire that will ask you questions about your health, family tree,
behaviors, and lifestyle. In addition, you may provide us with certain
electronic health record data and [
<i>describe other health data that CHONPS
HEALTH TECH seeks to collect]</i>.&nbsp; Completing a questionnaire and
providing this other Self-Reported information is completely voluntary.</span></p>
<p class="MsoNormal"><span>The information we gather from your Raw
Data and your Self-Reported Information helps us to create individualized Trait
information and reports that you can view and download through your CHONPS
Health Tech account.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>What kind of Traits can I learn about?</span></b></p>
<p class="MsoNormal"><span>The Trait analysis reports that we create
for and about you will provide interpretation of your genes. Through our
research and insights, we can give you different information about your Traits,
including your preferences, characteristics, psychological trends, preferences,
predispositions, behavior, attitudes, intelligence, abilities, and aptitudes.
The number and types of reports you get will depend on whether you are a free
or a paid user.</span></p>
<p class="MsoNormal"><span>The Traits we are able to analyze may
change as we grow and enhance our research. The research and science behind CHONPS
Health Tech is based on the current state of knowledge about the field of
genomics. Over time, we may learn more about DNA and how it affects various
Traits. As this knowledge improves, we may (at our sole discretion) choose to
update our research, reports, and the CHONPS Health Tech service we provide
you. As a result, your Trait analysis may change over time.</span></p>
<p class="MsoNormal"><span>CHONPS Health Tech does not currently
analyze or report on medical diseases or medical-related traits. Therefore,
genomic variants that might predict disease or carrier status (such as whether
you are a carrier for Tay-Sachs disease or cystic fibrosis) will not be analyzed
by us or identified in the CHONPS Health Tech report.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Who will be able to access my results?</span></b></p>
<p class="MsoNormal"><span>You, and any individual who you give access
to your CHONPS Health Tech account, will be able to access your Trait analysis
and reports.</span></p>
<p class="MsoNormal"><span>Our team may also be able to access your
results to create reports, improve your results, answer your questions, and
provide you with additional assistance that you may need from time to time. We
limit access to your results to our team members who have a legitimate reason
to access them for the purposes listed above. Please read our&nbsp;Privacy
Policy, which&nbsp;contains information about how we use and disclose the
Personal Information we collect about you while using CHONPS Health Tech.</span></p>
<p class="MsoNormal"><span>In addition, in the limited circumstances
described in our&nbsp;Privacy Policy, other third parties (such as our service
providers, research partners, and law enforcement/governmental entities) may be
able to access your results. We do not share your results or your identifiable
data with any other third parties or in any other circumstances except with
your consent.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Will CHONPS HEALTH TECH use my data for
purposes other than providing me with Trait analysis?</span></b></p>
<p class="MsoNormal"><span>We may use your data for purposes other
than providing you with your Trait analysis. Such purposes are described in our
Privacy Statement, and include the following:</span></p>
<ul>
  
<li class="MsoNormal"><span>To provide you with, personalize, improve and develop the CHONPS
     Health Tech service</span></li>
  
<li class="MsoNormal"><span>To share with you information about our products and services</span></li>
  
<li class="MsoNormal"><span>To contact you about research studies for which you may be
     eligible. You are under no obligation to participate in any research
     studies that we contact you about. If you choose to participate in one of
     our research studies, we will also use and disclose your data for research
     purposes as described in the applicable separate informed consent form
     that you must sign.</span></li>
  
<li class="MsoNormal"><span>To provide customer support to you</span></li>
  
<li class="MsoNormal"><span>To troubleshoot and protect the CHONPS Health Tech service</span></li>
  
<li class="MsoNormal"><span>To enforce our rights and for other legal purposes</span></li>
</ul>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span>In addition, we may aggregate your data
with other our other customers’ data for our own and our partners’ research,
product development and improvement, and marketing purposes. Aggregated data
cannot be used to identify you. For example, aggregated data may include a
statement that “30% of our female users share a particular genetic trait,”
without providing any data or Trait analysis specific to any individual user.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>What are the benefits of using CHONPS
Health Tech?</span></b></p>
<p class="MsoNormal"><span>We want you to benefit from using CHONPS
Health Tech and we hope you enjoy learning about your genetics. We aim to
empower you with knowledge about your DNA and Traits so that you can make
choices to improve your health, wellness, and interests.</span></p>
<p class="MsoNormal"><span>We also hope you use CHONPS Health Tech to
better understand how genetics works, including what your Raw Data looks like.
We have a number of features, including our Raw Data view, to help you visually
understand how your DNA data is analyzed based on growing genetics research.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>What are the risks of using CHONPS
Health Tech?</span></b></p>
<p class="MsoNormal"><span>There are some risks to using the CHONPS
Health Tech Service.</span></p>
<p class="MsoNormal"><span>There is a chance that you could learn
something about yourself that you did not want to know. For example, you may
learn that you are predisposed to sadness, anger, or loneliness, or that you
are likely to experience skin pigmentation or baldness. Since you share DNA
with your blood relatives, what you learn about yourself could also affect
them. You may want to discuss your options with a doctor, mental health
professional or genetic counselor before or after you get your results.</span></p>
<p class="MsoNormal"><span>There is a risk that your genetic
information could be used as a basis of discrimination. To address concerns
regarding possible health insurance and employment discrimination, many
countries (including the United States) have enacted laws to prohibit genetic
discrimination in those circumstances. The laws may not protect against genetic
discrimination in other circumstances such as when applying for life insurance,
disability insurance, or long-term care insurance. You should talk to your
physician or genetic counselor if you have concerns about genetic
discrimination.</span></p>
<p class="MsoNormal"><span>We may need to share details about you with
regulators and law enforcement. These details may include your Raw Data, Trait
analysis, or other Personal Information. We will only share these details if we
believe that the law or legal process requires us to do so. Please see
our&nbsp;Privacy Policy&nbsp;for more details.</span></p>
<p class="MsoNormal"><span>Finally, there is a risk that we experience
a security incident and, as a result, someone accesses your data and results
without authorization. This information could allow someone to connect your Raw
Data and other Personal Information back to you. We take steps to reduce the
risk of security incidents. Please see our Privacy Statement for more details.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>What are the limitations?</span></b></p>
<p class="MsoNormal"><span>CHONPS Health Tech has some limitations.
Some of these limitations are unique to CHONPS Health Tech, while other
limitations are related to Trait analysis in general. Many of these limitations
are discussed in our&nbsp;Terms of Use.</span></p>
<p class="MsoNormal"><span>Your Raw Data and Trait analysis cannot
tell you everything about you -- your DNA is only a part of who you are. The
analysis we do on your Raw Data, including any reports we create for you, is
not deterministic. In other words, the analysis and results describe your
probability of having a given Trait, and can only rarely predict when you have
that Trait for certain. In some cases, the choices you make about how you live
your life will influence your Traits more than your DNA.</span></p>
<p class="MsoNormal"><span>It is possible that the Raw Data you upload
to CHONPS Health Tech contains errors. In some cases, errors can occur when a
Third Party DNA Service sequences your DNA or reads the stored genetic
information. Because we do not, at this time, collect and test your DNA samples
ourselves, we are unable to identify the errors that might occur in the
processing of your DNA sample.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>How do I withdraw my consent?</span></b></p>
<p class="MsoNormal"><span>You can withdraw your consent at any time
by stopping your use of CHONPS Health Tech. You can also choose to close your CHONPS
Health Tech account. More details about closing your account and withdrawing
your consent can be found in our Privacy Statement and&nbsp;Terms of Use. If
you close your CHONPS Health Tech account, you will not be able to access your
information on CHONPS Health Tech moving forward. When you close your account,
we will archive your information. We will keep it archived for as long as we
need to meet our legal and regulatory requirements.</span></p>
<p class="MsoNormal"><span>If you withdraw your consent, we
discontinue the use of your data going forward. Withdrawing your consent does
not affect or nullify how we used your data in the past.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Additional important information</span></b></p>
<p class="MsoNormal"><span>We are not medical or healthcare
professionals. We do not provide medical advice, medical diagnosis, or
recommendations for medical treatment. We also do not provide genetic analysis
or reports regarding diseases or medical conditions. If you need advice
regarding diagnosis, treatment, or prevention of any disease, health, or
medical condition, you should consult your doctor or another qualified
healthcare professional.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Questions about CHONPS Health Tech</span></b></p>
<p class="MsoNormal"><span>If you have questions about CHONPS Health
Tech or what you are consenting to in this Informed Consent, you can contact us
at&nbsp;support@gene2h.com.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>Acknowledgment and Consent</span></b></p>
<p class="MsoNormal"><span>I acknowledge the following:</span></p>
<ul>
  
<li class="MsoNormal"><span>I have been offered the opportunity to ask questions about CHONPS
     Health Tech, including about the benefits, risks and limitations of using CHONPS
     Health Tech.</span></li>
  
<li class="MsoNormal"><span>I have read and understood this document in its entirety and
     realize I may retain a copy for my records.</span></li>
  
<li class="MsoNormal"><span>I have read and understood CHONPS HEALTH TECH’s&nbsp;Privacy
     Policy&nbsp;and&nbsp;Terms of Use.</span></li>
  
<li class="MsoNormal"><span>I confirm that I have the required and appropriate permission
     to upload my Raw Data (or the Raw Data of someone else) to CHONPS Health
     Tech.</span></li>
  
<li class="MsoNormal"><span>I consent to CHONPS HEALTH TECH analyzing my Raw Data and
     providing an analysis of my Traits based on CHONPS HEALTH TECH current
     knowledge and research.</span></li>
  
<li class="MsoNormal"><span>I consent to CHONPS HEALTH TECH’ ongoing analysis and use of my
     Raw Data as described herein.</span></li>
  
<li class="MsoNormal"><span>I consent to being contacted by or on behalf of CHONPS HEALTH
     TECH about research studies for which I may be eligible. I understand I am
     under no obligation to participate in any research studies about which I
     am contacted.</span></li>
  
<li class="MsoNormal"><span>I will discuss the results with my healthcare provider/genetic
     counselor if I have any medical or health-related questions or concerns.</span></li>
</ul>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span></span></p>]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=15&amp;l=tw</link>
      <category>15</category>
      <pubDate>2022-01-17 02:21:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Privacy Policy for use with direct raw DNA data upload 隱私政策（適用於自行上傳DNA數據文件的用戶）</title>
      <description><![CDATA[  <p class="MsoNormal">
<b><span>Privacy Policy&nbsp;</span></b></p>
<p class="MsoNormal"><span>Last Updated: January 17, 2022, effective
January 18, 2022</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span>This Privacy Policy describes how we
process the information we collect about you when you use the Services. We
define “Services” below, but it generally means the products and services that
we offer to you.</span></p>
<p class="MsoNormal"><span>Please carefully review this Privacy Policy
and let us know if you have any questions or concerns. We encourage you to
contact us, at any time, using the contact information in Section 16 below.</span></p>
<p class="MsoNormal"><span>Depending on how you use the Services, we
may ask you to sign an&nbsp;Informed Consent&nbsp;form that describes certain
aspects of the Services and asks for your consent to process your information
as part of those Services. To the extent that there is a conflict between this
Privacy Policy and an&nbsp;Informed Consent&nbsp;form that you have signed,
the&nbsp;Informed Consent&nbsp;form will control.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>1. . Key definitions</span></b></p>
<p class="MsoNormal">
<b><span>“Aggregate Information”</span></b><span>&nbsp;is information about multiple individuals that we have
combined so that no specific individual may be identified. Aggregate
Information is not Personal Information because it cannot be used to identify
you. For example, Aggregate Information may include a statement that “30% of
our female users share a particular genetic trait,” without providing any data
or testing results specific to any individual user.</span></p>
<p class="MsoNormal">
<i><span>“
<b>CHONPS HEALTH TECH</b>”</span></i><span>&nbsp;means CHONPS Health Tech, Inc. We will refer to CHONPS HEALTH
TECH as “we”, “us” and “our” throughout this Privacy Policy.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Cookie</b>”</span></i><span>&nbsp;is a text file that is placed on your hard disk by a web
server. Cookies are uniquely assigned to you, and can only be read by a web
server in the domain that issued the cookie to you. Cookies cannot be used to run
programs or deliver viruses to your computer. To learn more about Cookies,
visit&nbsp;www.allaboutcookies.org.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Data Collection Technologies</b>”</span></i><span>&nbsp;refer to Cookies, pixel tags, web beacons, and other
technologies that we or third parties use on our websites and other digital
services to collect information about your use of these services.</span></p>
<p class="MsoNormal">
<b>
<i><span>“De-Identified Data”</span></i></b><span>&nbsp;is data that cannot be used to infer information about, or be
linked to, an individual.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Designated European Countries</b></span></i><span>” means countries the European Economic Area, the United Kingdom,
and Switzerland.</span></p>
<p class="MsoNormal">
<i><span>“
<b>DNA</b>”</span></i><span>&nbsp;stands
for deoxyribonucleic acid, which is the molecule that contains your genetic
information. Your DNA is what makes you uniquely you.</span></p>
<p class="MsoNormal">
<b>
<i><span>“Genetic Information”</span></i></b><span>&nbsp;is any data concerning genetic material obtained from the
analysis of your biological sample by us or by Third Party DNA services.
Genetic Information includes, but is not limited to, DNA, Raw Data and Traits.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Personal Information</b>”</span></i><span>&nbsp;is information that identifies, relates to, describes, is
capable of being associated with, or could reasonably be linked, directly or
indirectly, with you or your household.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Raw Data</b>”</span></i><span>&nbsp;means information about your genotypes that is generated by
Third Party DNA Services. Your Raw Data contains the “letters” (nucleotides A,
C, G, T) that comprise DNA.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Sensitive Information</b></span></i><span>” is a subcategory of Personal Information that includes your racial
or ethnic origin, political opinions, religious or philosophical beliefs, trade
union membership, genetic information, biometric information, and information
concerning your health, sex life, or sexual orientation.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Service</b>”</span></i><span>&nbsp;means the CHONPS Health Tech™ service, associated websites (<a href="http://chonps.lanechen.xyz/">http://chonps.lanechen.xyz</a>, <a href="http://g2h.gene2h.com/">http://g2h.gene2h.com</a> &nbsp;and&nbsp;<a href="/">https://gene2h.com</a> ) and mobile applications, and
other ancillary or related services we offer from time to time.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Third Party DNA Services</b>”</span></i><span>&nbsp;means companies and organizations not related to or operated
by us that you may use to obtain DNA testing and results.</span></p>
<p class="MsoNormal">
<i><span>“
<b>Traits</b>”</span></i><span>&nbsp;means the characteristics or attributes that may be influenced
by your DNA. Your Traits may include your preferences, characteristics,
psychological trends, preferences, predispositions, behavior, attitudes,
intelligence, abilities, and aptitudes. The traits we analyze as part of the
Service are personal - not medical - in nature.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>2. Information we collect</span></b></p>
<p class="MsoNormal"><span>Depending on how you interact with or use
the Service, we may collect the following categories of Personal Information
about you:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Identifiers</span></b><span>, such as your name,
     postal address, email address, phone number, account username and
     password, image, and date of birth. We collect this information to
     identify you, provide you access to the Service, and communicate with you.</span></li>
  
<li class="MsoNormal">
<b><span>Genetic information</span></b><span>, including the
     information contained in your Raw Data and any Trait analysis we have
     performed on your Raw Data. We collect this information to provide you the
     Service. See more on the Section 3 “Genetic Information”.</span></li>
  
<li class="MsoNormal">
<b><span>Demographic information</span></b><span>, such as
     your race, ethnicity, gender, sexual orientation, and age. We collect this
     information to help you build your profile and tailor the services to you.</span></li>
  
<li class="MsoNormal">
<b><span>Physical and health-related information</span></b><span>, such as your height, weight, and medical history. We collect
     this information to help you build your profile and tailor the services to
     you.</span></li>
  
<li class="MsoNormal">
<b><span>Social media information</span></b><span>, such as
     your social media handle and related profile information. We typically
     only collect your social media information if you connect your social
     media account to the Service or otherwise interact with the Service using
     your social media account.</span></li>
  
<li class="MsoNormal">
<b><span>Device and other internet information</span></b><span>, such as your browsing history, search history, and the IP
     address, geolocation, and identification number of the device that you use
     to access the Service. We collect this information to enable and
     personalize your online experience.</span></li>
  
<li class="MsoNormal">
<b><span>Financial information</span></b><span>, such as your
     payment card information and billing/shipping address. We have engaged a
     third party payment processor to collect and process your payments on our
     behalf. We do not process or otherwise maintain your financial information
     on our systems or servers.</span></li>
</ul>
<p class="MsoNormal"><span>We may collect your Personal Information
directly from you, such as when you register for a CHONPS Health Tech account,
provide us with certain electronic health record data, complete a family
history questionnaire, survey or form, contribute to blogs and forums, or
contact us with a question.</span></p>
<p class="MsoNormal"><span>We may also collect your Personal
Information from third party sources, such as Third Party DNA Services, social
media platform providers, or your friends and family who refer our Service to
you. The Personal Information we collect from these third parties sources
typically depends on the privacy settings or permissions that you have
communicated with these third parties or otherwise set on their platforms.</span></p>
<p class="MsoNormal"><span>Finally, we may collect certain Personal
Information automatically through the use of Data Collection Technologies.
Please see Section 6 for more details about our use of Cookies and other Data
Collection Technologies.</span></p>
<p class="MsoNormal">
<b><span>Non-Personal Information.&nbsp;</span></b><span>We may also collect information that cannot be used to identify you.
This non-Personal Information may include Aggregate Information about our users
browser types, device types, and pages clicked. We collect this non-Personal
Information through server logs and Data Collection Technologies. We may
associate this information with the Personal Information that we collect about
you -- if we do, we will treat the combined information as Personal
Information.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>3. Genetic Information</span></b></p>
<p class="MsoNormal"><span>We collect your Genetic Information in the
following ways:</span></p>
<ul>
  
<li class="MsoNormal"><span>From third party sources, such as Third Party DNA services.
     This includes, but is not limited to, AncestryDNA, 23andMe, or MyHeritage.
     We receive your Raw Data that you obtain from these Third Party DNA
     services by consenting each services’ Terms of Use, Privacy Policy, or
     Informed Consent.&nbsp;</span></li>
</ul>
<p class="MsoNormal"><span>With your consent, we use your Genetic
Information for the following purposes:</span></p>
<ul>
  
<li class="MsoNormal">
<b>
<i><span>To provide the Service.&nbsp;</span></i></b><span>We
     process Personal Information in order to provide our Service, which
     includes processing payments, creating customer accounts and
     authenticating logins, analyzing Genetic Information, and delivering
     results.</span></li>
  
<li class="MsoNormal">
<b>
<i><span>To analyze and improve our Service.</span></i></b><span>&nbsp;We constantly work to improve and provide new reports,
     tools, and Services. We may also need to fix bugs or issues, analyze the
     use of our website to improve the customer experience or assess our
     marketing campaigns.</span></li>
  
<li class="MsoNormal">
<b>
<i><span>For CHONPS Health Tech Research, with your consent.</span></i></b><span>&nbsp;If you choose to consent to participate in CHONPS Health
     Tech Research, CHONPS Health Tech researchers can include your
     de-identified Genetic Information and Self-Reported Information in a large
     pool of customer data for analyses aimed at making scientific discoveries.</span></li>
</ul>
<p class="MsoNormal"><span>You may revoke your consent for the use of
your Genetic Information at any time by either deleting your data at&nbsp;<a href="https://g2h.gene2h.com/">https://g2h.gene2h.com/</a> &nbsp;(after logging
in) or contacting us at support@gene2h.com</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span>We disclose your Genetic Information as
follows:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>To you</span></b><span></span></li>
  
<li class="MsoNormal">
<b><span>With our service providers</span></b>
<b><span>,
     as necessary for them to provide their services to us.</span></b><span></span></li>
  
<li class="MsoNormal">
<b><span>With qualified research collaborators</span></b>
<b><span>, only if you provide your explicit consent.</span></b><span></span></li>
</ul>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span>CHONPS Health Tech will not sell, lease, or
rent your individual-level information to a third party for research purposes
without your explicit consent.</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>We will not</span></b>
<b><span> share your
     data with any </span></b>
<b><span>public
     databases</span></b>
<b><span>.</span></b><span></span></li>
  
<li class="MsoNormal">
<b><span>We will not</span></b>
<b><span> provide any
     person</span></b>
<b>’<span>s data (genetic or non-genetic) to an </span></b>
<b><span>insurance company</span></b>
<b><span> or </span></b>
<b><span>employer</span></b>
<b><span>.</span></b><span></span></li>
  
<li class="MsoNormal">
<b><span>We will not</span></b>
<b><span> provide
     information to </span></b>
<b><span>law enforcement</span></b>
<b><span> or </span></b>
<b><span>regulatory
     authorities</span></b>
<b><span> unless required by law to comply
     with a valid court order, subpoena, or search warrant for genetic or
     Personal Information.</span></b><span></span></li>
</ul>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>4. How we use your Personal Information</span></b></p>
<p class="MsoNormal"><span>In addition to the purposes for which we
collect your Personal Information listed in Section 2 above, we may use your
Personal Information for the following purposes:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>To provide the Service.</span></b><span>&nbsp;We use
     your Personal Information to create and maintain your CHONPS Health Tech
     account, enable purchases, process transactions, and provide other
     features and functionality to you.&nbsp;
<i>For individuals located in the
     Designated European Countries, our legal basis for processing your
     Personal Information is to provide our Service in accordance with
     our&nbsp;Terms of Use.</i></span></li>
  
<li class="MsoNormal">
<b><span>To personalize the Service.</span></b><span>&nbsp;We
     use your Personal Information to personalize and enhance your use of the
     Service, including to remember your preferences, provide personalized
     content, communications, and information, and track your use of the
     Service.&nbsp;
<i>For individuals located in the Designated European
     Countries, our legal basis for processing your Personal Information is our
     legitimate interest in delivering relevant and personalized content.</i></span></li>
  
<li class="MsoNormal">
<b><span>To processes, analyze, and deliver an analysis of your traits.</span></b><span>&nbsp;Once we receive your Raw Data, we will analyze it to
     provide individualized trait information and reports. We will also process
     and analyze your Personal Information pursuant to any informed consent you
     have signed.&nbsp;
<i>For individuals in Designated European Countries, our
     legal basis for processing your Personal Information is to provide our
     Service in accordance with our&nbsp;Terms of Use&nbsp;or pursuant to your
     consent.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To market to you.&nbsp;</span></b><span>We use your
     Personal Information to send you promotional or marketing messages, such
     as discounts, newsletters, and invitations to participate in surveys. You
     can unsubscribe from receiving these marketing communications by clicking
     the “unsubscribe” link in any marketing email we send you. You can also
     change your communication preferences in your CHONPS Health Tech account.
     Unsubscribing from marketing emails will not unsubscribe you from
     receiving non-marketing messages regarding your account, such as technical
     notices, purchase confirmations, or Service-related emails. &nbsp;
<i>If
     you are located in a Designated European Country, our legal basis for
     processing is our legitimate interest in providing information that may
     interest you, or otherwise your consent.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To improve and develop the Service.&nbsp;</span></b><span>We analyze your Personal Information to perform quality control
     activities, help us build new products, and improve the existing Service.
     We may also send you surveys, polls, or requests for testimonials to
     improve and optimize the Service.&nbsp;
<i>For individuals located in the
     Designated European Countries, our legal basis for processing your
     Personal Information is based on our legitimate interest. We think it is
     important to continue improving our Services to ensure your continued
     enjoyment.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To recruit you for research opportunities.&nbsp;</span></b><span>We may use your Personal Information to ask you if you would
     like to participate in research opportunities with us or our partners. If
     you decide to participate in a research opportunity, you may be asked to
     sign an informed consent to participate in this research.&nbsp;
<i>For
     individuals located in the Designated European Countries, our legal basis
     for processing your Sensitive Information is based on your consent.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To provide customer support.&nbsp;</span></b><span>If
     you contact us with a request, question or concern, we use your Personal
     Information, including Sensitive Information, as necessary to answer your
     questions, resolve disputes, and/or investigate and troubleshoot problems
     or complaints.&nbsp;
<i>For individuals located in the Designated European
     Countries, our legal basis for processing your Personal Information can be
     to satisfy our contractual or legal obligations and/or our legitimate
     interest to improve our Services, depending on the nature of your request.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To troubleshoot and protect the Service.&nbsp;</span></b><span>We use your Personal Information to help troubleshoot problems,
     authenticate your visits, and detect and prevent against error, fraud, or
     other criminal or malicious activity.&nbsp;
<i>For individuals located in
     the Designated European Countries, our legal basis for processing your
     Personal Information is to provide our Service in accordance with
     our&nbsp;Terms of Use&nbsp;and our legitimate interest of maintaining
     security.</i></span>
<b>‍</b><span></span></li>
  
<li class="MsoNormal">
<b><span>To enforce our rights and for other legal purposes.&nbsp;</span></b><span>We use your Personal Information to provide you with legally
     required notices, to enforce our&nbsp;
<i>Terms of Use</i>&nbsp;or to alert
     you to changes in our policies or agreements that may affect your use of
     the Service.&nbsp;
<i>For individuals located in the Designated European
     Countries, our legal basis for processing your Personal Information is to
     satisfy our contractual or legal&nbsp;</i>obligations
<i>.</i></span></li>
</ul>
<p class="MsoNormal"><span>If we need to collect Personal Information
by law or under the terms of a contract we have with you and you fail to
provide us with the information when requested, we may not be able to perform
the contract we have, or are trying to enter into, with you. We will inform you
of any Personal Information we require from you and the consequences if you
fail to provide it.</span></p>
<p class="MsoNormal">
<b><span>Special Categories:&nbsp;</span></b><span>We only process Special Categories of Personal Information if you
give us your explicit consent (such as through our&nbsp;Informed Consent), the
processing is necessary to meet a legal or regulatory obligation, the
processing is in connection with the establishment, exercise or defense of
legal claims, or is otherwise expressly permitted by law. Special Categories of
Personal Information includes information about your racial or ethnic origin,
genetic data (such as Raw Data), and data concerning health, sex life, and
sexual orientation.</span></p>
<p class="MsoNormal">
<b><span>Other Uses:&nbsp;</span></b><span>Any other purposes for which we wish to use your Personal
Information that are not listed above, or any other changes we propose to make
to the existing purposes will be notified to you by amending this Privacy
Policy in accordance with the Section 15.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>5. When we share your Personal
Information</span></b></p>
<p class="MsoNormal"><span>We may share your Personal Information in
the following circumstances:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>With service providers.</span></b><span>&nbsp;We may
     share your Personal Information with contractors and third-party service
     providers who help us to provide the Service and to understand how you use
     it (each, a “
<b>Subprocessor</b>"). Other categories service
     providers we use include marketing, operations, payment processing, and
     technology vendors. The list of examples of our Subprocessors can be
     found&nbsp;here.</span></li>
  
<li class="MsoNormal">
<b><span>With research partners.&nbsp;</span></b><span>We may
     share your Personal Information with research partners only when you opt
     in to share your data with those partners or you provide your consent to
     share your Personal Information by signing an informed consent form. Our
     research partners may include commercial or non-profit organizations that
     conduct or support scientific research, develop drugs or medical devices,
     or are generally interested in DNA analysis. In some circumstances, we or
     a research partner may have a financial interest in the research
     arrangement.&nbsp;</span></li>
</ul>
<p class="MsoNormal">
<i><span>Note: When we share your Personal
Information with research partners, we do not have control over how those
research partners use or disclose your Personal Information. We recommend that
you review the privacy policies of the research partners and any other third
party with whom you share, or ask us to share, your Personal Information.&nbsp;</span></i><span></span></p>
<ul>
  
<li class="MsoNormal">
<b><span>As required by law.&nbsp;</span></b><span>We may
     share your Personal Information where we, in good faith, believe that the
     law or legal process (such as a court order, search warrant or subpoena)
     requires us to do so; to investigate, prevent, or take action regarding
     illegal activities, suspected fraud, or violations of our&nbsp;
<i>Terms of
     Use</i>; or in other circumstances where we believe is necessary to
     protect the rights, safety or property of CHONPS HEALTH TECH, our users,
     and third parties.</span></li>
  
<li class="MsoNormal">
<b><span>As part of a business transaction.&nbsp;</span></b><span>In the event that CHONPS HEALTH TECH is involved in a business
     transaction such as a merger, acquisition, or sale of all or a portion of
     its assets, your Personal Information will likely be among the assets
     transferred. In such case, your Personal Information will remain subject
     to the provisions of this Privacy Policy.</span></li>
</ul>
<p class="MsoNormal">
<b><span>Sharing Aggregate Information.&nbsp;</span></b><span>We may share Aggregate Information with third parties or the general
public for our marketing or research purposes. For example, we may provide
Aggregate Information in commercial arrangements with our business partners so
that they may develop new research or products. We may also provide Aggregate
Information to advertisers so they may tailor marketing messages or
advertisements to our general user demographics. Disclosures for these purposes
will never contain your Personal Information.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>6. Viewing and correcting your Personal
Information</span></b></p>
<p class="MsoNormal"><span>You can log into your CHONPS Health Tech
account and view or amend the Personal Information associated with your account
at any time. Please note that if you amend the Personal Information in your
account, our servers may retain the old information as part of our logs and
backups.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>7. Cookie Policy</span></b></p>
<p class="MsoNormal"><span>This Cookie Policy explains what Cookies
are, the different types of Cookies, how we use them, and how you can control
them.</span></p>
<p class="MsoNormal"><span>We use both session and persistent Cookies
on our digital Service to improve your online experience. Session Cookies are
stored on your device during a single visit to the website, and they are
deleted as soon as you close your browser. Persistent Cookies remain on your
device until they expire or you choose to delete them from your browser cache,
and they are reactivated each time you visit the website that created them. You
can find out more about Cookies, learn about what cookies have been set, and
how you can manage and delete them at&nbsp;http://www.allaboutcookies.org.</span></p>
<p class="MsoNormal"><span>We use Cookies for the following purposes:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Authentication.&nbsp;</span></b><span>These Cookies
     help us ensure that your password works and that you stay logged in when
     you move between pages on the website. They also keep you secure while you
     are logged in and help to ensure the digital Service looks consistent
     during your visit.</span></li>
  
<li class="MsoNormal">
<b><span>Analytics.&nbsp;</span></b><span>We use analytics
     Cookies to collect information about how you use our digital Service, such
     as which pages you visit and if you experience any errors. Analytics
     Cookies collect only Aggregate Information and we use them to improve how
     our digital Service works, understand what interests our users, and
     measure how effective our content is. For example, we use Google Analytics
     to help us track and understand how users use our websites. For
     information about how Google uses the information it collects, please
     visit Google’s&nbsp;Terms of Service.</span></li>
  
<li class="MsoNormal">
<b><span>Advertising.&nbsp;</span></b><span>Advertising
     Cookies collect information about your browsing habits. We use them to
     tailor our advertising to your perceived interests. We work with third
     party partners to help us advertise around the Internet, as well as to
     allow advertisements to be placed on our digital Service. To opt out of
     some targeting cookies, see the Section titled “Online behavioral
     advertising” below.</span></li>
  
<li class="MsoNormal">
<b><span>Measurement.&nbsp;</span></b><span>We use other Data
     Collection Technologies to help us manage content on our digital Service
     by informing us what content is effective. We also use Data Collection
     Technologies in our HTML-based emails to let us know which emails have
     been opened by recipients. This allows us to gauge the effectiveness of
     certain communications.</span></li>
</ul>
<p class="MsoNormal">
<b><span>Controlling Cookies:&nbsp;</span></b><span>You can manage and block cookies by adjusting the settings in your
web browser. You can also set your browser to alert you every time a website
sets a Cookie. Each browser works differently, so please refer to your
browser’s help menu. Unless you have adjusted your browser settings, our system
will issue cookies as soon as you visit our digital Service. If you change your
browser settings to block all cookies (including essential ones) you may not be
able to access some or all parts of our digital Service.</span></p>
<p class="MsoNormal">
<b><span>DNT signals:</span></b><span>&nbsp;Some
web browsers incorporate a “Do Not Track” (“
<b>DNT</b>”) or similar feature
that signals to websites that a user does not want to have his or her online
activity and behavior tracked. Although we do our best to honor your privacy
preferences,, we do not respond to DNT signals from your browser at this time
due to the lack of an established industry standard.</span></p>
<p class="MsoNormal">
<b><span>Online behavioral advertising.&nbsp;</span></b><span>We may use Cookies to deliver content and advertisements specific to
your interests and online behavior. These advertisements may appear on our
digital Service or elsewhere on the Internet. We may also allow third-party
advertisers that are presenting advertisements for us to set and access their
cookies, pixels, tags, and scripts on your computer. The advertisers' use of
cookies and these other technologies is subject to their own privacy policies.
For information about online behavioral advertising and a tool that you can use
to opt out of such tracking, please visit the Network Advertising Initiative
website at&nbsp;http://www.networkadvertising.org/understanding-online-advertising&nbsp;or
the Digital Advertising Alliance website at&nbsp;http://www.aboutads.info.</span></p>
<p class="MsoNormal">
<b><span>Social Media Plug-Ins.&nbsp;</span></b><span>If you use buttons or plug-ins to share online content with your
friends via social networks like Twitter and Facebook, these companies may set
a Cookie on your computer or other device (laptop, tablet or mobile phone). To
find out more about the Cookies that these social media platforms, set, please
visit that social media platform’s privacy policy.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>8. Security</span></b></p>
<p class="MsoNormal"><span>We maintain reasonable and appropriate
safeguards designed to protect your Personally Information from unauthorized
access, use, disclosure, alteration or destruction. For example, we limit our
collection and use of your Personal Information to the extent necessary to
provide you with the Service. However, we cannot guarantee the security of our
systems or your Personal Information, and we encourage you to take reasonable
precautions to safeguard your Personal Data.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>&nbsp;9. Data retention</span></b></p>
<p class="MsoNormal"><span>We will keep your Personal Information for
as long as necessary to fulfill the purposes for which we collected it,
including any legal, professional, accounting or reporting requirements. To
determine the appropriate retention period, we consider the amount, nature, and
sensitivity of Personal Information, the potential risk of harm from
unauthorized use or disclosure of your Personal Information, the purposes for
which we process your Personal Information, whether we can achieve those
purposes through other means, and all applicable legal requirements.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>10. Users outside of Hong Kong</span></b></p>
<p class="MsoNormal"><span>We are committed to complying with this
Privacy Policy and the data protection laws, including those outside of Hong
Kong, that apply to our collection and use of your Personal Information. We are
located in Hong Kong and may use facilities in Hong Kong and other countries.
When you provide us with your Personal Information or use the Service, we will
process and store your Personal Information in Hong Kong and such other
countries where we have facilities. We recognize that the laws in Hong Kong and
such other countries may be different and, in some cases, not as protective as
the laws where you are located. By providing us with your Personal Information
or using the Service, you acknowledge that your Personal Information will be
transferred to and processed where we operate.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>11. Hong Kong privacy rights</span></b></p>
<p class="MsoNormal"><span>If you are a resident of Hong Kong, you may
be entitled to the following privacy rights:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>The right to know.&nbsp;</span></b><span>You have
     the right to request: (i) the specific pieces of Personal Information we
     have about you; (ii) the categories of Personal Information we have
     collected about you in the last 12 months; (iii) the categories of sources
     from which that Personal Information was collected; (iv) the categories of
     your Personal Information that we sold or disclosed in the last 12 months;
     (v) the categories of third parties to whom your Personal Information was
     sold or disclosed in the last 12 months; and (vi) the purpose for
     collecting and selling Personal Information. Generally:</span></li>
</ul>
<ul>
  
<li class="MsoNormal"><span>Within the preceding 12 months, CHONPS HEALTH TECH has
     collected the categories of personal information detailed in Section 2
     “Information We Collect” above from the sources described in Section 2.</span></li>
  
<li class="MsoNormal"><span>It is not our practice to sell Personal Information, including
     about children under 16 years old. However, we understand that under the Hong
     Kong Consumer Privacy Act, the use of certain types of Cookies may be
     considered a “sale” of Personal Information. If you have not opted out
     from the use of certain cookies within the preceding 12 months, your
     device and browsing information may have been used to serve you targeted
     advertisements.&nbsp;</span></li>
  
<li class="MsoNormal"><span>If you have provided your explicit consent, we have disclosed
     the following categories of Personal Information to our research partners
     within the preceding 12 months: Identifiers, Genetic information,
     Demographic information, Physical and health-related information; Social
     media information; Device and other internet information; and Financial
     information.</span></li>
  
<li class="MsoNormal">
<b><span>The right to deletion.&nbsp;</span></b><span>You
     have the right to request that we delete the Personal Information that we
     have collected or maintain about you. We may deny your request under
     certain circumstances, such as if we need to comply with our legal
     obligations or complete a transaction for which your Personal Information
     was collected. If we deny your request for deletion, we will let you know
     the reason why.</span></li>
  
<li class="MsoNormal">
<b><span>The right to opt out of the sale of your Personal
     Information.&nbsp;</span></b><span>You have the right to opt
     out of the sale of your Personal Information. If you wish to opt out of
     the use of your Personal Information for targeted advertising, please
     visit the Network Advertising Initiative website at&nbsp;http://www.networkadvertising.org/understanding-online-advertising&nbsp;or
     the Digital Advertising Alliance website at&nbsp;http://www.aboutads.info.</span></li>
  
<li class="MsoNormal">
<b><span>The right to equal service.&nbsp;</span></b><span>If
     you choose to exercise any of these rights, we will not discriminate
     against you in anyway. If you exercise certain rights, understand that you
     may be unable to use or access certain features of Service.</span></li>
</ul>
<p class="MsoNormal"><span>You may exercise your right to know and
your right to deletion twice a year free of charge. To exercise your right to
know or your right to deletion, email us at&nbsp;support@gene2h.com&nbsp;and
indicate “Hong Kong Rights” in the subject line.</span></p>
<p class="MsoNormal"><span>We will take steps to verify your identity
before processing your request to know or request to delete. We will not
fulfill your request unless you have provided sufficient information for us to
reasonably verify you are the individual about whom we collected Personal
Information. If you have an account with us, we will use our existing account
authentication practices to verify your identity. If you do not have an account
with us, we may request additional information about you to verify your
identity. We will only use the Personal Information provided in the
verification process to verify your identity or authority to make a request and
to track and document request responses, unless you initially provided the
information for another purpose.</span></p>
<p class="MsoNormal"><span>You may use an authorized agent to submit a
request to know or a request to delete. When we verify your agent’s request, we
may verify both your and your agent’s identity and request a signed document
from you that authorizes your agent to make the request on your behalf. To
protect your Personal Information, we reserve the right to deny a request from
an agent that does not submit proof that they have been authorized by you to
act on their behalf.</span></p>
<p class="MsoNormal">
<b><span>Shine the Light – Third Party
Marketing.&nbsp;</span></b><span>Hong Kong law permits individual Hong
Kong residents to request certain information regarding our disclosure of
certain categories of Personal Information to third parties for those third
parties’ direct marketing purposes. To make such a request, please contact us
using the information in Section 16. This request may be made no more than once
per calendar year, and we reserve our right not to respond to requests
submitted other than to the email or mailing addresses specified below.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>12. Hong Kong Genetic Information
Privacy Act</span></b></p>
<p class="MsoNormal"><span>If you are a resident of Hong Kong, you may
be entitled to the following rights regarding your Genetic Information:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Access:&nbsp;</span></b><span>You may access your
     Genetic Information.</span></li>
  
<li class="MsoNormal">
<b><span>Deletion</span></b><span>: You may delete your
     account and your Genetic Information, except for Genetic Information we
     are required to retain in order to comply with our legal obligations.</span></li>
  
<li class="MsoNormal">
<b><span>Destruction:</span></b><span>&nbsp;You may request
     that your biological sample be destroyed.</span></li>
  
<li class="MsoNormal">
<b><span>Non-discrimination</span></b><span>: If you exercise
     any of these rights, we will not discriminate against you. &nbsp;</span></li>
</ul>
<p class="MsoNormal"><span>To exercise these rights, you can
visit&nbsp;http://g2h.gene2h.com&nbsp;to delete your data or contact at support@gene2h.com.&nbsp;</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>13. Nevada Residents</span></b></p>
<p class="MsoNormal"><span>Pursuant to Nevada law, you may direct a
business that operates an internet website not to sell certain Personal
Information a business has collected or will collect about you. We do not sell
your Personal Information pursuant to Nevada law. For more information about
how we handle and share your Personal Information or your rights under Nevada
law, contact us at&nbsp;support@gene2h.com.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>14. Rights for individuals in the EEA</span></b></p>
<p class="MsoNormal"><span>If you are located in the European Economic
Area and we maintain your Personal Information, you have the following
additional rights (under the European Union’s General Data Protection
Regulation (the “
<b>GDPR</b>”) with regard to your Personal Information:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Right to access and receive:</span></b><span>&nbsp;You
     may request a copy of or access to the Personal Information we hold about
     you. You may also request that we transfer your Personal Information to a
     third party in a machine-readable format.</span></li>
  
<li class="MsoNormal">
<b><span>Right to correct:</span></b><span>&nbsp;You may ask
     us to update or correct inaccurate or incomplete Personal Information we
     hold about you.</span></li>
  
<li class="MsoNormal">
<b><span>Right to limit or restrict:&nbsp;</span></b><span>You
     may have the right to request that we stop using all or some of your
     Personal Information or to limit our use of it.</span></li>
  
<li class="MsoNormal">
<b><span>Right to erase:&nbsp;</span></b><span>You may have
     the right to request that we delete all or some of your Personal
     Information. This right may be limited if we have collected your Personal
     Information for research purposes.</span></li>
  
<li class="MsoNormal">
<b><span>Right to withdraw consent:&nbsp;</span></b><span>You
     have the right to withdraw any consent you have previously given to us at
     any time. Your withdrawal of consent does not affect the lawfulness of our
     collecting, using, and sharing of your Personal Information prior to the
     withdrawal of your consent. Even if you withdraw your consent, we have the
     right to use your Personal Information if it has been fully anonymized and
     cannot be used to personally identify you.</span></li>
  
<li class="MsoNormal">
<b><span>Right to complain:&nbsp;</span></b><span>You have
     the right to lodge a complaint with your Supervisory Authority if you are
     unhappy with how we process your Personal Information. You can find
     contact information for your Supervisory Authority on the European
     Commission Data Protection Authorities webpage or through other publicly
     available sources.</span></li>
</ul>
<p class="MsoNormal"><span>Please note that if you decide to exercise
some of your rights, we may be unable to provide you with certain services, or
you may not be able to use or take full advantage of the services we offer. We
may charge you a reasonable fee if you request additional copies of your
Personal Information or make other requests that are manifestly unfounded or
excessive. If we are unable to honor your request, or before we charge a fee,
we will let you know why.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>15. Children’s privacy</span></b></p>
<p class="MsoNormal"><span>Our services are not directed to or
intended for use by children. If we learn that we have received Personal Information
directly from a child without his or her parent or legal guardian’s verified
consent (where required by law), we will use that Personal Information only to
respond directly to that child (or his or her parent or legal guardian) to
inform the child that he or she cannot use our services. Subsequently, we will
delete such Personal Information.</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal">
<b><span>16. Third party websites and services</span></b></p>
<p class="MsoNormal"><span>When interacting with us, you may come
across links or references to third party websites and services that we do not
operate or control. If you provide your Personal Information to that third
party through its websites or services, you will be subject to that third
party’s privacy practices and policies and terms of use. This Privacy Policy
does not apply to any Personal Information that you provide to a third party
website or service. We recommend that you read the privacy policy that applies
to that third party website or service. A link or reference to a third party
website or service does not mean that we endorse that third party or the
quality or accuracy of the information presented on its website or service.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>17. Effective date; changes</span></b></p>
<p class="MsoNormal"><span>The last updated and effective date of this
Privacy Policy is posted at the top of this page. We may update this Privacy
Policy from time to time to reflect changes in our practices, our industry, or
applicable laws. When we make material changes to this Privacy Policy, we will
give you advance notice by posting an alert through the Service or by sending
you an email to the email address we have on file. The amended Privacy Policy
will apply on a go-forward basis to the Personal Information we already collected
about you, as well as any Personal Information we may collect in the future. If
you disagree with any changes, please let us know by contacting us using the
information in Section 16.</span></p>
<p class="MsoNormal">‍<span></span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal">
<b><span>18. Contact us</span></b></p>
<p class="MsoNormal"><span>If you have any questions or comments about
this Privacy Policy or our information practices, please contact us using the
following information:</span></p>
<p class="MsoNormal"><span>CHONPS Health Tech, Inc.<br /> Attn.: Privacy<br /> 
1F, 5 Sassoon Road, Pokfulam, Hong Kong</span></p>
<p class="MsoNormal"><span>support@gene2h.com</span></p>
<p class="MsoNormal"><span></span></p>
<p class="MsoNormal"><span>CHONPS Health Tech</span></p>
<p class="MsoNormal"><span>Copyright &copy; 2022. All rights reserved.</span></p>
<p class="MsoNormal"><span></span></p>]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=14&amp;l=tw</link>
      <category>14</category>
      <pubDate>2022-01-17 02:18:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Privacy Policy for use with order of Genetic Testing 隱私政策（適用於衕時訂購基因檢測服務的用戶）</title>
      <description><![CDATA[  <p class="MsoNormal" style="text-align:center;">
<b><span>Privacy Policy Highlights</span></b></p>
<p class="MsoNormal"><span>Last Updated: 16 Jan, 2022</span></p>
<p class="MsoNormal"><span>These "Privacy Highlights"
provide an overview of some core components of our data handling practices.
Please be sure to review the&nbsp;Full Privacy Statement.</span></p>
<p class="MsoNormal">
<b><span>Information We Collect</span></b></p>
<p class="MsoNormal"><span>We generally collect the following
information:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Information we receive when you use our Services.</span></b>
<b></b><span>&nbsp;We collect Web-Behavior Information via cookies and other
     similar tracking technologies when you use and access our Services (our
     website, mobile apps, products, software and other services). See
     our&nbsp;Cookie Policy</span><span>&nbsp;for more
     information.</span></li>
  
<li class="MsoNormal">
<b><span>Information you share with us.</span></b>
<b></b><span>&nbsp;We collect and process your information when you place an
     order, create an account, register your CHONPS Health Tech kit, complete
     research surveys, post on our Forums or use other messaging features, and
     contact Customer Care. This information can generally be categorized as
     Registration Information, Self-Reported Information, and/or User Content
     as defined in our full Privacy Statement.</span></li>
  
<li class="MsoNormal">
<b><span>Information from our DNA testing services.</span></b>
<b></b><span>&nbsp;With your consent, we extract your DNA from your saliva
     sample and analyze it to produce your Genetic Information (the As, Ts, Cs,
     and Gs at particular locations in your genome) in order to provide you
     with CHONPS Health Tech reports.</span></li>
</ul>
<p class="MsoNormal">
<b><span>How We Use Information</span></b></p>
<p class="MsoNormal"><span>We generally process Personal Information
for the following reasons:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>To provide our Services.</span></b><span> We
     process Personal Information in order to provide our Service, which
     includes processing payments, shipping kits to customers, creating
     customer accounts and authenticating logins, analyzing saliva samples and
     DNA, and delivering results and powering tools like DNA Relatives.</span></li>
  
<li class="MsoNormal">
<b><span>To analyze and improve our Services.</span></b>
<b></b><span>&nbsp;We constantly work to improve and provide new reports,
     tools, and Services. For example, we are constantly working to improve our
     ability to assign specific ancestries to your DNA segments and maximize
     the granularity of our results. We may also need to fix bugs or issues,
     analyze the use of our website to improve the customer experience or
     assess our marketing campaigns.</span></li>
  
<li class="MsoNormal">
<b><span>For CHONPS Health Tech Research, with your consent.</span></b><span> If you choose to consent to participate in CHONPS Health Tech
     Research, CHONPS Health Tech researchers can include your de-identified
     Genetic Information and Self-Reported Information in a large pool of
     customer data for analyses aimed at making scientific discoveries.</span></li>
</ul>
<p class="MsoNormal">
<b><span>Control: Your Choices</span></b></p>
<p class="MsoNormal"><span>You have the ability to make decisions
about how your data is shared and used. You choose:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>To store or discard your saliva sample</span></b>
<b></b><span>&nbsp;after it has been analyzed.</span></li>
  
<li class="MsoNormal">
<b><span>Which health report(s)</span></b>
<b></b><span>&nbsp;you view and/or opt-in to view.</span></li>
  
<li class="MsoNormal"><span>When and with whom </span>
<b><span>you share
     your information</span></b>
<b></b><span>, including
     friends, family members, health care professionals, or others outside our
     Services, including through third party services that accept CHONPS Health
     Tech data and social networks.</span></li>
  
<li class="MsoNormal"><span>To give or decline consent for CHONPS Health Tech Research. By
     agreeing to the Research Consent Document, Individual Data Sharing Consent
     Document, or participating in a CHONPS Health Tech Research Community you
     can consent to the use of your de-identified data for scientific research
     purposes.</span></li>
  
<li class="MsoNormal"><span>To delete your CHONPS Health Tech account and data, at any
     time.</span></li>
</ul>
<p class="MsoNormal">
<b><span>Access To Your Information</span></b></p>
<p class="MsoNormal"><span>Your Personal Information may be shared in
the following ways:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>With our service providers</span></b><span>,
     as necessary for them to provide their services to us.</span></li>
  
<li class="MsoNormal">
<b><span>With qualified research collaborators</span></b>
<b></b><span>, only if you provide your explicit consent.</span></li>
</ul>
<p class="MsoNormal"><span>CHONPS Health Tech will not sell, lease, or
rent your individual-level information to a third party for research purposes
without your explicit consent.</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>We will not</span></b>
<b></b><span>&nbsp;share
     your data with any </span>
<b><span>public databases</span></b>
<b></b><span>.</span></li>
  
<li class="MsoNormal">
<b><span>We will not</span></b>
<b></b><span>&nbsp;provide
     any person’s data (genetic or non-genetic) to an </span>
<b><span>insurance company</span></b>
<b></b><span>&nbsp;or&nbsp;</span>
<b><span>employer</span></b>
<b></b><span>.</span></li>
  
<li class="MsoNormal">
<b><span>We will not</span></b><span> provide
     information to </span>
<b><span>law enforcement</span></b><span> or&nbsp;</span>
<b><span>regulatory
     authorities</span></b><span> unless required by law to comply
     with a valid court order, subpoena, or search warrant for genetic or
     Personal Information (visit our&nbsp;</span><span>Transparency
     Report</span><span>).</span></li>
</ul>
<p class="MsoNormal">
<b><span>How We Secure Information</span></b></p>
<p class="MsoNormal"><span>CHONPS Health Tech implements measures and
systems to ensure confidentiality, integrity, and availability of CHONPS Health
Tech data. Our team regularly reviews and improves our security practices to
help ensure the integrity of our systems and your information. These practices
include, but are not limited to, the following areas:</span></p>
<ul>
  
<li class="MsoNormal">
<b><span>Independent security certification and audit.</span></b><span> Our information security management system, which protects CHONPS
     Health Tech information assets supporting our Services, has been certified
     under the internationally recognized ISO/IEC 27001:2013 standard. Some of
     those controls are described below.</span></li>
  
<li class="MsoNormal">
<b><span>Encryption.</span></b>
<b></b><span>&nbsp;CHONPS
     Health Tech uses industry standard security measures to encrypt Sensitive
     Information both when it is stored and when it is being transmitted.</span></li>
  
<li class="MsoNormal">
<b><span>Limited access to essential personnel.</span></b>
<b></b><span>&nbsp;We limit access of information to authorized personnel,
     based on job function and role. CHONPS Health Tech access controls include
     multi-factor authentication, single sign-on, and a strict least-privileged
     authorization policy.</span></li>
</ul>
<p class="MsoNormal">
<b><span>Risks and Considerations</span></b></p>
<p class="MsoNormal"><span>There may be some consequences of using our
Services that you haven't considered.</span></p>
<ul>
  
<li class="MsoNormal"><span>You may discover things about yourself and/or your family
     members that may be upsetting or cause anxiety and that you may not have
     the ability to control or change.</span></li>
  
<li class="MsoNormal"><span>You may discover relatives who were previously unknown to you,
     or may learn that someone you thought you were related to is not your
     biological relative.</span></li>
  
<li class="MsoNormal"><span>In the event of a data breach it is possible that your data
     could be associated with your identity, which could be used against your
     interests.</span></li>
</ul>
<p class="MsoNormal"><span>Full Privacy Statement</span></p>
<p class="MsoNormal"><span>Last Updated: 16 Jan, 2022</span></p>
<p class="MsoNormal"><span>This Privacy Statement applies to all
websites owned and operated by CHONPS Health Tech, Inc ("CHONPS Health
Tech"), including&nbsp;www.gene2h.com, and any other websites, pages,
features, or content we own or operate, and to your use of the CHONPS Health
Tech mobile app and any related Services. Our Privacy Statement is designed to
help you better understand how we collect, use, store, process, and transfer
your information when using our Services.</span></p>
<p class="MsoNormal"><span>Please carefully review this Privacy
Statement and our&nbsp;Terms of Service. Unless otherwise defined in this
Privacy Statement, terms used in this Privacy Statement have the same meanings
as terms defined in our&nbsp;Terms of Service. By using our Services, you
acknowledge all of the policies and procedures described in the foregoing
documents. If you do not agree with or you are not comfortable with any aspect
of this Privacy Statement or our Terms of Service, you should immediately
discontinue use of our Services.</span></p>
<p class="MsoNormal">
<b><span>Contents</span></b><span></span></p>
<ol>
  
<li class="MsoNormal"><span>Key Definitions</span></li>
  
<li class="MsoNormal"><span>Information we collect</span></li>
  <ul>
    
<li class="MsoNormal"><span>Information you provide directly to us</span></li>
    
<li class="MsoNormal"><span>Information related to our genetic testing services</span></li>
    
<li class="MsoNormal"><span>Information collected through tracking technology</span></li>
    
<li class="MsoNormal"><span>Other types of information</span></li>
  </ul>
  
<li class="MsoNormal"><span>How we use your information</span></li>
  <ul>
    
<li class="MsoNormal"><span>To provide you with Services and analyze and improve our
      Services</span></li>
    
<li class="MsoNormal"><span>To process, analyze and deliver your genetic testing results</span></li>
    
<li class="MsoNormal"><span>To allow you to share your Personal Information with others</span></li>
    
<li class="MsoNormal"><span>To allow you to share your Personal Information for research
      purposes</span></li>
    
<li class="MsoNormal"><span>To recruit you for external research</span></li>
    
<li class="MsoNormal"><span>To provide customer support</span></li>
    
<li class="MsoNormal"><span>To conduct surveys or polls, and obtain testimonials</span></li>
    
<li class="MsoNormal"><span>To provide you with marketing communications</span></li>
  </ul>
  
<li class="MsoNormal"><span>Information we share with third parties</span></li>
  <ul>
    
<li class="MsoNormal"><span>General Service Providers</span></li>
    
<li class="MsoNormal"><span>"Targeted advertising" service providers</span></li>
    
<li class="MsoNormal"><span>Aggregate Information</span></li>
    
<li class="MsoNormal"><span>Information we share with commonly owned entities</span></li>
    
<li class="MsoNormal"><span>As required by law</span></li>
    
<li class="MsoNormal"><span>Business Transactions</span></li>
  </ul>
  
<li class="MsoNormal"><span>Your choices</span></li>
  <ul>
    
<li class="MsoNormal"><span>Access to your account</span></li>
    
<li class="MsoNormal"><span>Marketing communications</span></li>
    
<li class="MsoNormal"><span>Sharing outside of the CHONPS Health Tech Services</span></li>
    
<li class="MsoNormal"><span>Account Deletion</span></li>
  </ul>
  
<li class="MsoNormal"><span>Security Measures</span></li>
  
<li class="MsoNormal"><span>Children's Privacy</span></li>
  
<li class="MsoNormal"><span>Linked Websites</span></li>
  
<li class="MsoNormal"><span>Information for Customers in Designated Countries</span></li>
  <ul>
    
<li class="MsoNormal"><span>International Transfers</span></li>
    
<li class="MsoNormal"><span>Our relationship with you</span></li>
    
<li class="MsoNormal"><span>Legal bases for processing Personal Information from the EU</span></li>
    
<li class="MsoNormal"><span>Direct Marketing</span></li>
    
<li class="MsoNormal"><span>Privacy Rights</span></li>
    
<li class="MsoNormal"><span>Complaints</span></li>
  </ul>
  
<li class="MsoNormal"><span>California </span><span>Residents</span></li>
  
<li class="MsoNormal"><span>Nevada Residents</span></li>
  
<li class="MsoNormal"><span>Do-Not-Track Statement</span></li>
  
<li class="MsoNormal"><span>Changes to this Privacy Statement</span></li>
  
<li class="MsoNormal"><span>Contact information</span></li>
</ol>
<p class="MsoNormal">
<b><span>1. Key Definitions</span></b><span></span></p>
<ol>
  
<li class="MsoNormal">
<b><span>Aggregate Information</span></b><span>: information
     that has been combined with that of other users and analyzed or evaluated
     as a whole, such that no specific individual may be reasonably identified.</span></li>
  
<li class="MsoNormal">
<b><span>De-identified Information</span></b><span>:
     information that has been stripped of your Registration Information (e.g.,
     your name and contact information) and other identifying data such that
     you cannot reasonably be identified as an individual, also known as
     pseudonymized information.</span></li>
  
<li class="MsoNormal">
<b><span>Individual-level Information</span></b><span>:
     information about a single individual's genotypes, diseases or other
     traits/characteristics, but which is not necessarily tied to Registration
     Information.</span></li>
  
<li class="MsoNormal">
<b><span>Personal Information</span></b><span>: information
     that can be used to identify you, either alone or in combination with
     other information. CHONPS Health Tech collects and stores the following
     types of Personal Information:</span></li>
</ol>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">a.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Registration Information</span></b><span>: information you provide about yourself when registering for and/or
purchasing our Services (e.g. name, email, address, user ID and password, and
payment information).</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">b.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Genetic Information</span></b><span>: information regarding your genotypes (i.e. the As, Ts, Cs, and Gs
at particular locations in your genome), generated through processing of your
saliva by CHONPS Health Tech or by its contractors, successors, or assignees; or
otherwise processed by and/or contributed to CHONPS Health Tech.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">c.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Self-Reported Information</span></b>
<b></b><span>: information you provide directly to us, either through the
Services or through a third party, including your disease conditions, other
health-related information, personal traits, ethnicity, family history, and
other information that you enter into surveys, forms, or features while signed
in to your CHONPS Health Tech account.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">d.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Sensitive Information</span></b><span>: information about your health, Genetic Information, and certain
Self-Reported Information such as racial and ethnic origin, sexual orientation,
and political affiliation.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">e.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>User Content</span></b><span>: information, data, text, software, music, audio, photographs,
graphics, video, messages, or other materials - other than Genetic Information
and Self-Reported Information-generated by users of CHONPS Health Tech Services
and transmitted, whether publicly or privately, to or through CHONPS Health
Tech.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">f.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Inferences and Derived Data</span></b><span>: information, data, assumptions, or conclusions that are derived
directly or indirectly from another source of Personal Information. For
example, we may use statistical techniques to infer additional genetic
information based on genetic information generated directly through the
processing of your saliva sample.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">g.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Web-Behavior Information</span></b><span>: information on how you use our Services collected through log
files, cookies, web beacons, and similar technologies, (e.g., device
information (device identifiers), IP address, browser type, domains, page
views).</span></p>
<p class="MsoNormal">
<b><span>2. Information we collect</span></b><span></span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">a.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Information you provide
directly to us or through a third party</span></b><span></span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.
<b><span>Registration
Information.</span></b><span>&nbsp;</span><span>When you
purchase our Services or create a CHONPS Health Tech account, we collect
Personal Information, which may include your name, date of birth, billing and
shipping address, payment information (e.g., credit card) and contact
information (e.g. email, phone number and license number).</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.
<b><span>Self-Reported
Information.</span></b><span>&nbsp;</span><span>You have
the option to provide us with additional information about yourself through
surveys, forms, features and applications. For example, you may provide us with
information about your personal traits (e.g., eye color, height), ethnicity,
disease conditions (e.g., Type 2 Diabetes), other health-related information
(e.g., pulse rate, cholesterol levels, visual acuity), and family history
information (e.g., information similar to the foregoing about your family
members). Before you disclose information about a family member, you should
make sure you have permission from the family member to do so.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iii.
<b><span>User
Content.</span></b><span>&nbsp;Some of our Services allow you to
create and post or upload content, such as data, text, software, music, audio,
photographs, graphics, video, messages, or other materials that you create or
provide to us through either a public or private transmission ("
<b>User
Content</b>"). For example, User Content includes any discussions, posts,
or messages you send on our Forums.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iv.
<b><span>Blogs
and Forums.</span></b><span>&nbsp;Our website offers publicly
accessible blogs. Additionally, CHONPS Health Tech customers may participate in
our online Forums. You should be aware that any information you provide or post
in these areas may be read, collected, and used by others who access them. To
request that we remove or de-identify your Personal Information from our blog
or Forums, contact us at&nbsp;privacy@gene2h.com. Please note that whenever you
post something publicly, it may sometimes be impossible to remove all instances
of the posted information, for example, if someone has taken a screenshot of
your posting. Please exercise caution before choosing to share Personal
Information publicly on our blogs, Forums or in any other posting. You may be
required to register with a third party application to post a comment. To learn
how the third party application uses your information, please review the third
party's terms of use and privacy statement.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">v.
<b><span>Social
media features and widgets.</span></b><span>&nbsp;Our Services
include Social Media Features, such as the Facebook "Like" or
"Share" button and widgets ("Features"). These Features may
collect your IP address, which page you are visiting on our site, and may set a
cookie to enable the Feature to function properly. They may also allow third
party social media services to provide us information about you, including your
name, email address, and other contact information. The information we receive
is dependent upon your privacy settings with the third party social media
service. Features are either hosted by a third party or hosted directly on our
site. Your interactions with these Features are governed by the privacy
statements of the third party companies providing them. You should always
review and, if necessary, adjust your privacy settings on third party websites
and services before linking or connecting them to our website or Service.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">vi.
<b><span>Third
party services (e.g., social media).</span></b><span>&nbsp;If you
use a third party site, such as Facebook or Twitter, in connection with our
Services to communicate with another person (e.g., to make or post referrals or
to request that we communicate with another person), then in addition to that
person's name and contact information, we may also collect other information
(e.g., your profile picture, network, gender, username, user ID, age range,
language, country, friends lists or followers) depending on your privacy
settings on the third party site. We do not control the third party site's
information practices, so please review the third party’s privacy statement and
your settings on the third party’s site carefully.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">vii.
<b><span>Third
party sign in.</span></b><span>&nbsp;You may create a CHONPS Health
Tech account and/or sign in to our Services using an account you created with a
third party service, such as Google. If you provide authorization to CHONPS
Health Tech, we will collect and use the information you share with us via that
third party service (such as your email address, name, and date of birth as
specified in your third party service account) in accordance with this Privacy
Statement. You are responsible for managing your credentials for your third
party service account, and for maintaining the security of your third party
service account. CHONPS Health Tech does not have access to the credentials for
your third party service account. If you choose to use third party sign in and
you lose access to your credentials for your third party service account, you
may not be able to access your CHONPS Health Tech account. You may manage
authorization for third party sign in through your CHONPS Health Tech Account
Settings or through your third party service account.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">viii.
<b><span>Referral
information and sharing.</span></b><span>&nbsp;When you refer a
person to CHONPS Health Tech or choose to share your CHONPS Health Tech results
with another person, we will ask for that person's email address. We will use
their email address solely, as applicable, to make the referral or to
communicate your sharing request to them, and we will let your contact know
that you requested the communication. By participating in a referral program or
by choosing to share information with another person, you confirm that the
person has given you consent for CHONPS Health Tech to communicate (e.g., via
email) with him or her. The person you referred may contact us at&nbsp;privacy@gene2h.com&nbsp;to
request that we remove this information from our database. For more information
on our referral program, see&nbsp;here.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ix.
<b><span>Gifts.</span></b><span>&nbsp;If you provide us with Personal Information about others, if
others give us your information, or if you authorize another individual to
share or send your Personal Information to our third party service provider(s)
for the purpose of ordering the Service or other personalized gift(s), we will
only use that information for the purpose for which it was provided to us.
These purposes may include, for example, where you provide us with a friend’s
shipping address when placing an order or where you authorize a family member
to order personalized merchandise based on your ancestry report results. Once a
gift recipient registers for our Services and agrees to our&nbsp;Privacy
Statement, our&nbsp;Terms of Service, and if applicable, certain&nbsp;Consent
Documents, his or her Personal Information will be used in manners consistent
with this Privacy Statement, and will not be shared with the purchaser, unless
they independently choose to share their own Personal Information through the
Services with the purchaser. Information shared directly with our third party
service provider(s) for personalized gifts are subject to such third party’s
terms of service and privacy policies.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">x.
<b><span>Customer
service.</span></b><span>&nbsp;When you contact&nbsp;Customer Care&nbsp;or
correspond with us about our Service, we collect information to: track and
respond to your inquiry; investigate any breach of our&nbsp;Terms of Service,&nbsp;Privacy
Statement&nbsp;or applicable laws or regulations; and analyze and improve our
Services.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">b.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Information related to our
genetic testing services</span></b><span></span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">&nbsp;.
<b><span>Saliva sample and biobanking.</span></b><span>&nbsp;To
use our genetic testing services, you must purchase, or receive as a gift, a CHONPS
Health Tech Personal Genetic Service testing kit, create an online account and
register your kit, and ship your saliva sample to us or our third party
laboratory. Your DNA will be extracted from your saliva sample for analysis.
During kit registration you are asked to review our&nbsp;Consent Document for
Sample Storage and Additional Genetic Analyses. Unless you consent to sample
storage (“Biobanking”) and additional analyses, your saliva sample and DNA are
destroyed after the laboratory completes its work, subject to laboratory legal
and regulatory requirements. You can update your Biobanking preference to
discard a stored sample within your CHONPS Health Tech Account Settings once
your sample has completed processing.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.
<b><span>Genetic
Information.&nbsp;</span></b><span>Information regarding your
genotype (e.g. the As, Ts, Cs, and Gs at particular locations in your genome),
your Genetic Information, is generated when we analyze and process your saliva
sample, or when you otherwise contribute or access your Genetic Information
through our Services. Genetic Information includes the CHONPS Health Tech results
reported to you as part of our Services, and may be used for other purposes, as
outlined in Section 3 below.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">c.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Web-Behavior Information
collected through tracking technology (e.g. from cookies and similar
technologies)</span></b><span></span></p>
<p class="MsoNormal"><span>We and our third party service providers
use cookies and similar technologies (such as web beacons, tags, scripts and
device identifiers) to:</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">&nbsp;.<span>help us recognize you when you use our Services;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.<span>customize
and improve your experience;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.<span>provide
security;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iii.<span>analyze
usage of our Services (such as to analyze your interactions with the results,
reports, and other features of the Service);</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iv.<span>gather
demographic information about our user base;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">v.<span>offer our
Services to you;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">vi.<span>monitor the
success of marketing programs; and</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">vii.<span>serve
targeted advertising on our site and on other sites around the Internet.</span></p>
<p class="MsoNormal"><span>If you reject cookies, you may still use
our site, but your ability to use some features or areas of our site may be
limited. For more information, including the types of cookies found on CHONPS
Health Tech and how to control cookies, please read our&nbsp;Cookie Policy.</span></p>
<p class="MsoNormal"><span>We may receive reports based on the use of
these technologies from third party service providers as de-identified,
Individual-level Information or as Aggregate Information (as described in
Section 4.c).</span></p>
<p class="MsoNormal">
<b><span>Google Analytics.</span></b><span>&nbsp;Google Analytics is used to perform many of the tasks listed
above. We use the User-ID feature of Google Analytics to combine behavioral
information across devices and sessions (including authenticated and
unauthenticated sessions). We have enabled the following Google Analytics
Advertising features: Remarketing, Google Display Network Impression Reporting,
Google Analytics Demographics and Interest Reporting, and DoubleClick Campaign
Manager integration. We do not merge information collected through any Google
advertising product with individual-level information collected elsewhere by
our Service.&nbsp;
<b>Learn more about how Google collects and uses data&nbsp;here</b>.
To opt out of Google Analytics Advertising Features please use&nbsp;Google Ad
Settings. To opt out of Google Analytics entirely please use&nbsp;this link.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">d.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Other Types of Information</span></b><span></span></p>
<p class="MsoNormal"><span>We continuously work to enhance our
Services with new products, applications and features that may result in the
collection of new and different types of information. We will update our
Privacy Statement and/or obtain your prior consent to new processing, as
needed.</span></p>
<p class="MsoNormal">
<b><span>3. How we use your information</span></b><span></span></p>
<p class="MsoNormal"><span>CHONPS Health Tech will use and share your
Personal Information with third parties only in the ways that are described in
this Privacy Statement.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">a.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To provide you with Services
and to analyze and improve our Services</span></b><span></span></p>
<p class="MsoNormal"><span>We use the information described above in
Section 2 to operate, provide, analyze and improve our Services. These
activities may include, among other things, using your information in a manner
consistent with this Privacy Statement to:</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.<span>open your
account, enable purchases and process payments, communicate with you, and
implement your requests (e.g., referrals);</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.<span>enable and
enhance your use of our website and mobile application(s), including
authenticating your visits, providing personalized content and information, and
tracking your usage of our Services;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iii.<span>contact
you about your account, and any relevant information about our Services (e.g.
policy changes, security updates or issues, etc.);</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iv.<span>enforce our
Terms of Service and other agreements;</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">v.<span>monitor,
detect, investigate and prevent prohibited or illegal behaviors on our
Services, to combat spam and other security risks; and</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">vi.<span>perform
research &amp; development activities, which may include, for example,
conducting data analysis in order to develop new or improve existing products
and services, and performing quality control activities.</span></p>
<p class="MsoNormal"><span>For individuals located in the European
Economic Area (“EEA”), United Kingdom, or Switzerland (collectively the “Designated
Countries”): We process your Personal Information in this way to provide our
Services to you in accordance with our&nbsp;Terms of Service.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">b.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To process, analyze and
deliver your genetic testing results</span></b><span></span></p>
<p class="MsoNormal"><span>As described above, to receive results
through the Personal Genetic Service, you must create a CHONPS Health Tech
account, register your kit, and submit your saliva sample to be genotyped by us
or our contracted laboratory. Once genotyped, we further analyze your Genetic
Information to provide you with our health and/or ancestry reports, depending
on the Service purchased. CHONPS Health Tech continuously works to improve our
Services based on our research and product development, and genetic
associations identified in scientific literature. If you are eligible to
receive additional reports or updates in the future, you may be notified of or
may directly access these updates.</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Sensitive Information for the
purposes described above is based on your consent. You may withdraw your
consent at any time by deleting your Account via your CHONPS Health Tech
Account Settings, however, the withdrawal of your consent will not affect the
lawfulness of processing based on consent before its withdrawal.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">c.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To allow you to share your
Personal Information with others</span></b><span></span></p>
<p class="MsoNormal"><span>CHONPS Health Tech gives you the ability to
share information, including Personal Information, through the Services. You
have the option to share directly with individuals with CHONPS Health Tech
accounts through (i) our Forums, (ii) relative finding features (e.g.,
"DNA Relatives"), and (iii) other sharing features and tools. You may
also have the ability to share information directly with individuals who have
not participated in our Service via a unique, shareable URL or through a social
media platform (such information is "User Content"). Some sharing
features, including receiving sharing invitations, may require that you
opt-out, however you will always be required to take a positive action, such as
opting in, to share Sensitive Information.</span></p>
<p class="MsoNormal"><span>You should be thoughtful about your sharing
choices. Once you have chosen to share any Personal Information, the
individuals with whom you share this information, may also use or share your Personal
Information, including any Sensitive Information you choose to share.</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Personal Information for the
purpose described above is based on your consent. You may withdraw your consent
at any time, however, the withdrawal of your consent will not affect the
lawfulness of processing based on consent before its withdrawal.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">d.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To allow you to share your
Personal Information for CHONPS Health Tech Research purposes</span></b><span></span></p>
<p class="MsoNormal"><span>You have the choice to participate in CHONPS
Health Tech Research by providing your consent. "CHONPS Health Tech
Research" refers to research aimed at publication in peer-reviewed
journals and other research funded by the federal government (such as the
National Institutes of Health (“NIH”)) conducted by CHONPS Health Tech.</span></p>
<p class="MsoNormal"><span>CHONPS Health Tech Research may be
sponsored by, conducted on behalf of, or in collaboration with third parties,
such as non-profit foundations, academic institutions or pharmaceutical
companies. CHONPS Health Tech Research may study a specific group or population,
identify potential areas or targets for therapeutics development, conduct or
support the development of drugs, diagnostics or devices to diagnose, predict
or treat medical or other health conditions, work with public, private and/or
non-profit entities on genetic research initiatives, or otherwise create,
commercialize, and apply this new knowledge to improve health care. CHONPS
Health Tech Research uses Aggregate and/or Individual-level&nbsp;Genetic
Information&nbsp;and&nbsp;Self-Reported Information&nbsp;as specified in the
appropriate Consent Document(s), as explained in greater detail below.</span></p>
<p class="MsoNormal"><span>Your De-identified Genetic and
Self-Reported Information may be used for CHONPS Health Tech Research only if
you have consented to this use by completing a Consent Document. If you have
completed the main Research&nbsp;Consent Document:</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">&nbsp;.<span>Your&nbsp;Genetic Information&nbsp;and/or&nbsp;Self-Reported
Information&nbsp;will be used for research purposes, but it will be
de-identified and will not be linked to your Registration Information.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.<span>CHONPS
Health Tech may use individual-level&nbsp;Genetic Information&nbsp;and&nbsp;Self-Reported
Information&nbsp;internally at CHONPS Health Tech for research purposes.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.<span>CHONPS
Health Tech may share summary statistics, which do not identify any particular
individual or contain individual-level information, with our qualified research
collaborators.</span></p>
<p class="MsoNormal"><span>If you have completed the&nbsp;Individual
Level Data Sharing Consent, or additional consent agreement, in addition to the
uses above under the main Research Consent Document, CHONPS Health Tech may
share De-identified Individual-level Genetic Information and Self-Reported
Information with select third party research collaborators for CHONPS Health
Tech Research purposes.</span></p>
<p class="MsoNormal">
<b><span>Withdrawing your Consent.</span></b><span> You may withdraw your consent to participate in CHONPS Health Tech
Research at any time by changing your consent status within your CHONPS Health
Tech Account Settings. If you experience difficulties changing your consent
status, contact the Human Protections Administrator at&nbsp;hpa@CHONPS Health
Tech.com</span><span>. CHONPS Health Tech will not include your </span><span>Genetic Information</span><span>&nbsp;or&nbsp;Self-Reported
Information</span><span>&nbsp;in studies that start more than 30
days after you withdraw (it may take up to 30 days to withdraw your information
after you withdraw your consent). Any research involving your data that has
already been performed or published prior to your withdrawal from CHONPS Health
Tech Research will not be reversed, undone, or withdrawn. You may also
discontinue your participation in CHONPS Health Tech Research by deleting your CHONPS
Health Tech account (as described in Section 5.d.).</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Sensitive Information for the
purpose described above is based on your consent. You may withdraw your consent
at any time, however, the withdrawal of your consent will not affect the
lawfulness of processing based on consent before its withdrawal.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">e.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To recruit you for external
research</span></b><span></span></p>
<p class="MsoNormal"><span>Research is an important aspect of our
Services and we want to ensure interested participants are aware of additional
opportunities to contribute to interesting, novel scientific research conducted
by academic institutions, healthcare organizations, pharmaceutical companies,
and other groups. If you have chosen to participate in CHONPS Health Tech
Research, from time to time we may inform you of third party research
opportunities for which you may be eligible. For example, if a university tells
us about a new cancer research project, we may send an email to CHONPS Health
Tech research participants who potentially fit the relevant eligibility
criteria to make them aware of the research project and provide a link to
participate with the research organization conducting the study. We will not
share Individual-level Genetic Information or Self-Reported Information with
any third party without your explicit consent. If you do not wish to receive
these notifications, you can manage them by editing your preferences in your CHONPS
Health Tech Account Settings.</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Sensitive Information for the
purpose described above is based on your consent. You may withdraw your consent
at any time, however, the withdrawal of your consent will not affect the
lawfulness of processing based on consent before its withdrawal.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">f.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To provide customer support</span></b><span></span></p>
<p class="MsoNormal"><span>When you contact Customer Care, we may use
or request Personal Information, including Sensitive Information, as necessary
to answer your questions, resolve disputes, and/or investigate and troubleshoot
problems or complaints. In some instances, we may be required to process one
customer’s Personal Information to resolve another customer’s dispute or
request. For example, if a customer reports behavior that violates our Terms of
Service, we will separately process both customers’ Personal Information and
respond separately to each individual as appropriate. We will not share your
Personal Information with another customer without your consent.</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Personal Information for the purpose
described above depends on the nature of the customer support request. Our
legal basis can be to satisfy our contractual or legal obligations and/or our
legitimate interest to improve our Services.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">g.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To conduct surveys or polls,
and obtain testimonials</span></b><span></span></p>
<p class="MsoNormal"><span>We value your feedback and may send you
surveys, polls, or requests for testimonials to improve and optimize our
Services. You are in control of the information you would like to share with
us. If you do not wish to receive these requests, you can manage them in your CHONPS
Health Tech Account Settings.</span></p>
<p class="MsoNormal"><span>For individuals located in the Designated
Countries: Our legal basis for processing your Personal Information for the
purpose described above is based on our legitimate interest. We think it is
important to continue improving our Services to ensure your continued
enjoyment.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">h.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>To provide you with
marketing communications</span></b><span></span></p>
<p class="MsoNormal"><span>By creating a CHONPS Health Tech account,
you are agreeing that we may send you product and promotional emails or
notifications about our Services, and offers on new products, services,
promotions or contests. You may also opt-in to receiving similar notifications
on the website or mobile application(s). You can unsubscribe from receiving
these marketing communications at any time. To unsubscribe, click the email footer
“unsubscribe” link or go to the “Preferences” section of your CHONPS Health
Tech Account Settings to edit your email notification preferences. To opt-out
of receiving website and mobile notifications, you may do so within your
browser or device settings. Please note, the opt-out process differs between
web browsers and mobile devices. You may not opt-out of receiving
non-promotional messages regarding your account, such as technical notices,
purchase confirmations, or Service-related emails.</span></p>
<p class="MsoNormal"><span>Individuals located in Designated Countries
should review Section 9.d. to understand our marketing practices in relation to
the Designated Countries.</span></p>
<p class="MsoNormal">
<b><span>4. Information we share with third
parties</span></b><span></span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">a.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>General service providers.</span></b><span></span></p>
<p class="MsoNormal"><span>We share the information described above in
Section 2 with our third party service providers, as necessary for them to
provide their services to us and help us perform our contract with you. Service
providers are third parties (other companies or individuals) that help us to
provide, analyze and improve our Services. While CHONPS Health Tech directly
conducts the majority of data processing activities required to provide our
Services to you, we engage some third party service providers to assist in
supporting our Services, including in the following areas:</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.
<b><span>Order
fulfillment and shipping.</span></b>
<b></b><span>&nbsp;Our
payment processor processes certain Registration Information, such as your
billing address and credit card information, as necessary to enable you to
purchase a CHONPS Health Tech kit from the CHONPS Health Tech.com online store.
Our distribution centers ship your kit(s) to you, and in some cases help return
your kit safely to us or to our third party laboratory so your sample can be
processed.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.
<b><span>Our
CLIA-certified genotyping lab.</span></b>
<b></b><span>&nbsp;To use our
genetic testing services, you must purchase, or receive as a gift, a CHONPS
Health Tech Personal Genetic Service testing kit, and ship your saliva sample
to us or our third party laboratory. Once delivered, receiving personnel at the
laboratory remove and discard kit packaging, which in some cases may contain
"sender information" (e.g., name, address), before testing personnel
receive the samples for processing. Receiving personnel do not perform testing,
and testing personnel handle saliva samples that are only identified by a
unique barcode. For samples processed by our third party genotyping laboratory,
when the laboratory has completed their analysis, they securely send the
resulting Genetic Information to us identified by your unique barcode.</span></p>
<p class="MsoNormal"><span>During kit registration, you are asked to
review our Consent Document for Sample Storage and Additional Genetic Analyses.
Unless you consent to Biobanking and additional analyses, your saliva sample
and DNA are destroyed after the laboratory completes its work, subject to the
legal and regulatory requirements. Should you wish to update your sample
storage preference to discard a stored sample, you can do so within your CHONPS
Health Tech Account Settings once your sample has completed processing. As
detailed further in Section 5.d. (Account Deletion), our genotyping laboratory
or contracted genotyping laboratory will retain certain information as
necessary to comply with applicable regulatory and legal obligations.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iii.
<b><span>Customer
Care support.</span></b><span>&nbsp;Our Customer Care team uses a
number of tools to help organize and manage the requests we receive. These
tools help to ensure we provide timely, high quality support.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">iv.
<b><span>Cloud
storage, IT, and Security.</span></b><span>&nbsp;Our cloud storage
providers provide secure storage for information in CHONPS Health Tech
databases, ensure that our infrastructure can support continued use of our
Services by CHONPS Health Tech customers, and protect data in the event of a
natural disaster or other disruption to our Service. Our IT and security
service providers assist with intrusion detection and prevention measures to
stop any potential attacks against our networks. We have these third party experts
perform regular penetration tests and periodically audit CHONPS Health Tech’s
security controls.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">v.
<b><span>Marketing
and analytics.</span></b><span>&nbsp;When you use our Services,
including our website or mobile app(s), our third party service providers may
collect Web-Behavior Information about your visit, such as the links you
clicked on, the duration of your visit, and the URLs you visited. This
information can help us improve site navigability and assess our Marketing
campaigns. Per applicable data protection regulations, our EU, UK, and International
websites present visitors with a cookie opt in to allow the processing
described above via Functionality and Advertising Cookies.</span></p>
<p class="MsoNormal"><span>NOTE: Our service providers act on CHONPS
Health Tech's behalf. We implement procedures and maintain contractual terms
with each service provider to protect the confidentiality and security of your
information. However, we cannot guarantee the confidentiality and security of
your information due to the inherent risks associated with storing and
transmitting data electronically.</span></p>
<p class="MsoNormal"><span>For individuals located in the European
Economic Area (“EEA”), United Kingdom, or Switzerland (collectively the
“Designated Countries”): Where Personal Information are transferred to a third
country or to an international organisation, CHONPS Health Tech implements appropriate
safeguards, such as contractual obligations, relating to the transfer.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">b.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>"Targeted
advertising" service providers</span></b><span></span></p>
<p class="MsoNormal"><span>We permit third party advertising networks
and providers to collect Web-Behavior Information regarding the use of our
Services to help us to deliver targeted online advertisements ("ads")
to you. They use cookies and similar technologies, to gather information about
your browser's or device's visits and usage patterns on our Services and on
other websites over time, which helps to better personalize ads to match your
interests, and to measure the effectiveness of ad campaigns. We and our third
party service providers will not use your Sensitive Information, such as&nbsp;Genetic
Information&nbsp;and&nbsp;Self-Reported Information, for targeted marketing
without asking for and receiving your explicit consent.</span></p>
<p class="MsoNormal"><span>For more information about our marketing
practices, please review our&nbsp;Cookie Policy.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">c.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Aggregate information</span></b><span></span></p>
<p class="MsoNormal"><span>We may share Aggregate Information, which
is information that has been stripped of your name and contact information and
combined with information of others so that you cannot reasonably be identified
as an individual, with third parties. This Information is different from
"Individual-level" information and is not Personal Information because
it does not identify any particular individual or disclose any particular
individual’s data. For example, Aggregate Information may include a statement
that "30% of our female users share a particular genetic trait,"
without providing any data or testing results specific to any individual user.
In contrast, Individual-level Genetic Information&nbsp;or Self-Reported
Information consists of data about a single individual's genotypes, diseases or
other traits/characteristics information and could reveal whether a specific
user has a particular genetic trait, or consist of all of the Genetic
Information about that user. CHONPS Health Tech will ask for your consent to
share Individual-level Genetic Information or Self-Reported Information with
any third party, other than our service providers as necessary for us to
provide the Services to you.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">d.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Information we share with
commonly owned entities</span></b><span></span></p>
<p class="MsoNormal"><span>We may share some or all of your Personal
Information with other companies under common ownership or control of CHONPS
Health Tech, which may include our subsidiaries, our corporate parent, or any
other subsidiaries owned by our corporate parent in order to provide you better
service and improve user experience. Generally, sharing such information is
necessary for us to perform on our contract with you. We may provide additional
notice and ask for your prior consent if we wish to share your Personal
Information with our commonly owned entities in a materially different way than
discussed in this Privacy Statement.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">e.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>As required by law</span></b><span></span></p>
<p class="MsoNormal"><span>Under certain circumstances your Personal
Information may be subject to processing pursuant to laws, regulations,
judicial or other government subpoenas, warrants, or orders. For example, we
may be required to disclose Personal Information in coordination with
regulatory authorities in response to lawful requests by public authorities,
including to meet national security or law enforcement requirements. CHONPS
Health Tech will preserve and disclose any and all information to law
enforcement agencies or others if required to do so by law or in the good faith
belief that such preservation or disclosure is reasonably necessary to: (a)
comply with legal or regulatory process (such as a judicial proceeding, court
order, or government inquiry) or obligations that CHONPS Health Tech may owe
pursuant to ethical and other professional rules, laws, and regulations; (b)
enforce the CHONPS Health Tech&nbsp;Terms of Service&nbsp;and other policies;
(c) respond to claims that any content violates the rights of third parties; or
(d) protect the rights, property, or personal safety of CHONPS Health Tech, its
employees, its users, its clients, and the public. View our&nbsp;Transparency
Report&nbsp;for more information.</span></p>
<p class="MsoNormal"><span>NOTE: If you are participating in CHONPS
Health Tech Research, CHONPS Health Tech will withhold disclosure of your
Personal Information involved in such Research in response to judicial or other
government subpoenas, warrants or orders in accordance with any applicable
Certificate of Confidentiality that CHONPS Health Tech has obtained from the
National Institutes of Health (NIH). There are limits to what the Certificate
of Confidentiality covers so please visit the&nbsp;Certificates of Confidentiality
Kiosk.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">f.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Business transactions</span></b><span></span></p>
<p class="MsoNormal"><span>In the event that CHONPS Health Tech goes
through a business transition such as a merger, acquisition by another company,
or sale of all or a portion of its assets your Personal Information will likely
be among the assets transferred. In such a case, your information would remain
subject to the promises made in any pre-existing Privacy Statement.</span></p>
<p class="MsoNormal">
<b><span>5. Your choices</span></b><span></span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">a.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Access to your account</span></b><span></span></p>
<p class="MsoNormal"><span>We provide access to your CHONPS Health
Tech data within your CHONPS Health Tech account. You can access and download data
processed by CHONPS Health Tech within your CHONPS Health Tech Account Settings
and within applicable Reports, Tools, and features. If you lose access to your CHONPS
Health Tech account or account email address, please contact Customer Care for
assistance. If you lose access to your CHONPS Health Tech account, in certain
circumstances, we may require that you submit additional information sufficient
to verify your identity before providing access or otherwise releasing
information to you. If you choose not to submit the required documentation, or
the information provided is not sufficient for the purposes sought, CHONPS
Health Tech will not be able to sufficiently verify your identity in order to
complete your request.</span></p>
<p class="MsoNormal"><span>You may access, correct or update most of
your&nbsp;Registration Information&nbsp;on your own within your CHONPS Health
Tech Account Settings. You may also review and update your consent to CHONPS
Health Tech Research and Biobanking. You may be able to correct Self-Reported
Information entered into a survey, form, or feature within your account, such
as on the&nbsp;surveys page, by clicking “Edit your answers here.” Please note
that you may not be able to delete User Content that has been shared with
others through the Service and that you may not be able to delete information
that has been shared with third parties.</span></p>
<p class="MsoNormal"><span>Individuals located in Designated Countries
should review Section 9.e. to understand their rights to access Personal
Information.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">b.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Marketing communications</span></b><span></span></p>
<p class="MsoNormal"><span>As noted in Section 3.h. you may be asked
to opt-in to receive product and promotional emails or notifications when
creating your CHONPS Health Tech account or when using our Services. You may
view or update your notification preferences for marketing communications by
visiting your CHONPS Health Tech Account Settings, opting out at the browser or
device level, or by contacting our Privacy Administrator at&nbsp;privacy@gene2h.com.
You can also click the "unsubscribe" button at the bottom of
promotional email communications, as applicable.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">c.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Sharing outside of the CHONPS
Health Tech Services</span></b><span></span></p>
<p class="MsoNormal"><span>You may decide to share your Personal
Information with friends and/or family members, doctors or other health care
professionals, and/or other individuals outside of our Services, including
through third party services such as social networks and third party apps that
connect to our website and mobile apps through our application programming
interface ("API"). These third parties may use your Personal
Information differently than we do under this Privacy Statement. Please make
such choices carefully and review the privacy statements of all other third
parties involved in the transaction. CHONPS Health Tech does not endorse or
sponsor any API applications, and does not affirm the accuracy or validity of
any interpretations made by third party API applications.</span></p>
<p class="MsoNormal"><span>In general, it can be difficult to contain
or retrieve Personal Information once it has been shared or disclosed. CHONPS
Health Tech will have no responsibility or liability for any consequences that
may result because you have released or shared Personal Information with
others. Likewise, if you are reading this because you have access to the
Personal Information of a CHONPS Health Tech customer through a multi-profile
account, we urge you to recognize your responsibility to protect the privacy of
each person within that account. Users with multi-profile accounts (i.e., where
multiple family members register their kits to one account) should use caution
in setting profile-level privacy settings.</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">d.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<b><span>Account deletion</span></b><span></span></p>
<p class="MsoNormal"><span>If you no longer wish to participate in our
Services, or no longer wish to have your Personal Information be processed, you
may delete your CHONPS Health Tech account and Personal Information within your
CHONPS Health Tech Account Settings. Once you submit your request, we will send
an email to the email address linked to your CHONPS Health Tech account
detailing our account deletion policy and requesting that you confirm your
deletion request. Once you confirm your request to delete your account and
data, your account will no longer be accessible while we process your request.
Once you confirm your request, this process cannot be cancelled, undone,
withdrawn, or reversed. When your account is deleted, all associated Personal
Information is deleted and any stored samples are discarded, subject to the
following limitations:</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">i.<span>Information
previously included in CHONPS Health Tech Research. As stated in any applicable
Consent Document, Genetic Information and/or Self-Reported Information that you
have previously provided and for which you have given consent to use in CHONPS
Health Tech Research cannot be removed from completed studies that use that
information. Your data will not be included in studies that start more than 30
days after your account is closed (it may take up to 30 days to withdraw your
information after your account is closed).</span></p>
<p class="MsoNormal" style="margin-left:0cm;text-indent:0cm;">ii.<span>Legal
Retention Requirements. CHONPS Health Tech and/or our contracted genotyping
laboratory will retain your Genetic Information, date of birth, and sex as
required for compliance with applicable legal obligations, including the
federal Clinical Laboratory Improvement Amendments of 1988 (CLIA), California
Business and Professions Code Section 1265 and College of American Pathologists
(CAP) accreditation requirements. CHONPS Health Tech will also retain limited
information related to your account and data deletion request, including but
not limited to, your email address, account deletion request identifier,
communications related to inquiries or complaints and legal agreements for a
limited period of time as required by law, contractual obligations, and/or as
necessary for the establishment, exercise or defense of legal claims and for
audit and compliance purposes.</span></p>
<p class="MsoNormal">
<b><span>6. Security measures</span></b><span></span></p>
<p class="MsoNormal"><span>CHONPS Health Tech takes seriously the
trust you place in us. CHONPS Health Tech implements physical, technical, and
administrative measures to prevent unauthorized access to or disclo]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=13&amp;l=tw</link>
      <category>13</category>
      <pubDate>2022-01-16 08:31:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>研髮中</title>
      <description><![CDATA[  G4B 英文版]]></description>
      
<link>https://gene2h.com/index.php?m=page&amp;f=view&amp;t=xml&amp;articleID=12&amp;l=tw</link>
      <category>12</category>
      <pubDate>2022-01-16 08:30:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>PGS step by step: a brief pipeline</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_8196fbd7153babb846f11c8bb5fc41f6&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_4ac70da1574a9e817328ce8f4da7401c&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_5778b7cda0c6dc1125f222cf55c78c88&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_d195ee7e1930795de40e83a0ce0334dd&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_2a7e518a26b2e0110cdfe29f3a426b74&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_82d92891b0d7ddc41b1faa564e9f2e83&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_5d01e85df767cc59522b335fcba7b407&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_52383df9467cb195a709bff589841527&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_87b71d3148a72f7930d8e6eb2f6fc494&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_c2c75c6cb03e8444ca9a9caddc243233&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_d8febce6fa9b0986a30edb85e56db410&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_12a7ac1232ee8278c45605fed1600edf&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_463d06b7faa42d1c568ce6141c6a9835&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_e1e49071759ab7075a198189e1ea6f1a&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_051f9598f1ff7e19a02d823afa250f8f&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_9a384d14f6aa9572ee973c03efb79c24&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_c994a5fefaded2623e22aa95622791fe&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_7188fe0803b600a9e26aa2fb44608ac2&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_44b10f258bb35ac9a64a12f47a867d0c&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_26f75c2b53c777ffae18fd5a230603cf&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_1e8e2bae78cebc72a2940d192b8f41d8&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_59fe329852b3965342a680118ac29bde&t=png&o=&s=&v=1642265463" alt width="800" height="597" title align /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_50d89aeff735529fe2971804f7755e4f&t=png&o=&s=&v=1642265463" alt width="800" height="750" title align /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=11&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 02:11:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>How do we evaluate Polygenic Scoring?</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_fdaac2c5bd20546c8b115262383d7015&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_147253910d348b49d1334743d7c40b53&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_577c2f79d8e8b23ff6c5c43c191f4cf2&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_87e5789c4dbd9db0f0a79e63aac093ad&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_eced7797dcc6010d8e44c7345f00e8a9&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_927e5a9a817f7cca7d755cf572569125&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_3b7d56be8877eb98292738c74feb039c&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_22e7927bb7a3b180e916a98011effbf4&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_473bd8aea82f89bbe5fad98748a69bac&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_8b855e6a30e6fde537e0736ff041c870&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=10&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 02:08:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Which Polygenic Scoring method is better?</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_75a9b706c8614f434400764c0338527c&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_decce3c38733dab713d3a6514552b893&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_b6a6e3d94d5a9fe0b772cc20c96fcad1&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_a6c91db346dc69333fb43a013523bc63&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_2a4274aaf4f4d0605bb47a3c88c11694&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_007b5a7e19bcb2e3cafdd307c4487f0d&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=9&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 02:04:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>The toolkit for modelling PGS</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_646281966a30b57895298f9eee3e9d62&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_bc8d9c8e6cb93877b68d567866ad959b&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_c41cc65f28680aadbb0dcdba0cce32c9&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_5a77a3090bc54b098e86b6aa944d937d&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=8&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 02:02:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>The history of PGS: since 2009</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_01d46b74c9737bfe784fd3873d713812&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_e73c045a8bd46314dead4d1c3d0986f1&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_419dbb3ec059218e164254ca44a9e354&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_49f5876a32a58696fefdeb2682263058&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_08aba7cc071d7c49fe41cfed431eef58&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_d41a1885c8cdd662d37f5e6f629c0a7e&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_e269e661d85b20cccb5778d88ee02fe7&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=7&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 01:57:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>The Background of Polygenic Scoring</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_22b83cbfdf4ce08422ec007f64e64606&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_9c1beafb498f7ad85fd2688e36d55891&t=png&o=&s=&v=1642265463" alt /></p>
<p><br /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_536a84f6e1a1722602432f3b8c515523&t=png&o=&s=&v=1642265463" alt /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_3302ec2e4ffd6de4bb1e41357676c2f7&t=png&o=&s=&v=1642265463" alt /></p>
<p><br /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_06621d52ae88347820c5fdfdcedc43f4&t=png&o=&s=&v=1642265463" alt /></p>
<p><br /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_a894b68c3633776baa441d60b13f7572&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=article&amp;f=view&amp;t=xml&amp;articleID=6&amp;l=tw</link>
      <category>科學原理 The Science of Polygenic Scoring</category>
      <pubDate>2022-01-16 01:47:00 +0800</pubDate>
    </item>
  
    <item>
      
<title>Polygenic Scoring has great research utilities</title>
      <description><![CDATA[  <p>
<img src="https://gene2h.com/file.php?f=202201/f_a788292d4a8a5b4e940a2bfeacef1893&t=png&o=&s=&v=1642265463" alt /></p>
<p><br /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_d62ebad0c61e9775040e1f22b7e03e33&t=png&o=&s=&v=1642265463" alt /></p>
<p><br /></p>
<p>
<img src="https://gene2h.com/file.php?f=202201/f_037fe294e675a713e3189e9dd68093e4&t=png&o=&s=&v=1642265463" alt /></p>]]></description>
      
<link>https://gene2h.com/index.php?m=blog&amp;f=view&amp;t=xml&amp;articleID=5&amp;l=tw</link>
      <category>The Benefits of PGS</category>
      <pubDate>2022-01-16 01:25:00 +0800</pubDate>
    </item>
  
  
    <item>
      
<title>G2H-2C-EN</title>
      <description><![CDATA[  
<img src="https://gene2h.com/file.php?f=202403/f_47d13ab56d64f913d4482061e4edc39e&t=png&o=&s=&v=1711231395" alt />]]></description>
      
<link>https://gene2h.com/index.php?m=product&amp;f=view&amp;t=xml&amp;productID=4&amp;l=tw</link>
      <category>G2H-2C</category>
      <pubDate>2024-03-24 06:18:35 +0800</pubDate>
    </item>
  
    <item>
      
<title>G4B中文版</title>
      <description><![CDATA[  <p class="MsoNormal">我們利用<span lang="EN-US">Polygenic scoring</span>技術在原有<span lang="EN-US">GBLUP</span>預測模型基礎上改進<span lang="EN-US">30%-50%</span>都準確率，從而極大地提高基因組育種的效率<span lang="EN-US"><o:p></o:p></span></p>]]></description>
      
<link>https://gene2h.com/index.php?m=product&amp;f=view&amp;t=xml&amp;productID=3&amp;l=tw</link>
      <category>G4B-2B</category>
      <pubDate>2022-01-16 06:00:23 +0800</pubDate>
    </item>
  
    <item>
      
<title>G2H中文版</title>
      <description><![CDATA[  <p class="MsoNormal">上傳您的DNA數據文件，以穫取最新的健康風險預測分析報告，涵蓋超過800種疾病與性狀</p>
<p class="MsoNormal">
<img src="https://gene2h.com/file.php?f=202403/f_d671a47d5a47373fb90c8bdfa04eac3e&t=png&o=&s=&v=1711232310" alt /></p>
<p class="MsoNormal"><br /></p>
]]></description>
      
<link>https://gene2h.com/index.php?m=product&amp;f=view&amp;t=xml&amp;productID=2&amp;l=tw</link>
      <category>G2H-2C</category>
      <pubDate>2022-01-16 05:59:24 +0800</pubDate>
    </item>
  
    <item>
      
<title>G2H</title>
      <description><![CDATA[  <p class="MsoNormal"><span lang="EN-US">G2H (developed by CHONPS Health Tech) is
the most advanced and comprehensive platform for health prediction and risk
management<o:p></o:p></span></p>]]></description>
      
<link>https://gene2h.com/index.php?m=product&amp;f=view&amp;t=xml&amp;productID=1&amp;l=tw</link>
      <category>基因智健 Gene-to-Health (G2H)</category>
      <pubDate>2022-01-16 05:58:20 +0800</pubDate>
    </item>
  
    <item>
      
<title>G2H-CVD1.0</title>
      <description><![CDATA[  <p><strong>Welcome to G2H-CVD1.0 - Predict Your 10-Year Cardiovascular Disease Risk</strong></p>
<p>At G2H, we believe in empowering individuals to take control of their heart health with cutting-edge tools. Our <strong>G2H-CVD1.0</strong> is a powerful risk prediction model designed to assess your 10-year risk of developing cardiovascular disease (CVD).</p>
<h3>How It Works:</h3>
<ol>
  
<li><strong>Simple Inputs:</strong> Enter your basic health information, such as age, sex, cholesterol levels, blood pressure, and lifestyle factors.</li>
  
<li><strong>Advanced Predictive Model:</strong> Using state-of-the-art algorithms, <strong>G2H-CVD1.0</strong> analyzes your data to generate a personalized risk assessment for cardiovascular disease over the next 10 years.</li>
  
<li><strong>Get Your Free Report:</strong> Once you complete the input, you will receive a <strong>detailed risk prediction report</strong> along with personalized recommendations to improve your heart health.</li>
</ol>
<h3>Why Use G2H-CVD1.0?</h3>
<ul>
  
<li><strong>Accurate Predictions:</strong> G2H-CVD1.0 uses scientifically validated models to give you a reliable prediction.</li>
  
<li><strong>Personalized Recommendations:</strong> Based on your results, you’ll get tailored suggestions to improve your health.</li>
  
<li><strong>Completely Free:</strong> No hidden costs or requirements, just input your details and get your risk report.</li>
</ul>
<h3>Start Your Risk Prediction Today:</h3>
<p>Click on the button below to get started with the <strong>G2H-CVD1.0</strong> prediction tool.</p>
<p><a rel="noopener" target="_new" href="https://g2h.lanechen.xyz"><strong>Try G2H-CVD1.0 Now</strong></a></p>
<p>Beta version:</p>
<p>https://cvd.gene2h.com</p>
<p>Stable version:</p>
<p>https://gene2health.shinyapps.io/ASCVD_Risk_Evaluation/</p>]]></description>
      
<link>https://gene2h.com/index.php?m=product&amp;f=view&amp;t=xml&amp;productID=5&amp;l=tw</link>
      <category>G2H-2C</category>
      <pubDate>2025-02-05 12:04:53 +0800</pubDate>
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