檢索結果 - Andrew G. Sharo

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  1. 1
    StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants

    StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants 由 Andrew G. Sharo, Zhiqiang Hu, Shamil Sunyaev, Steven E. Brenner

    出版 2022
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    Artigo
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  2. 2
    ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden

    ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden 由 Andrew G. Sharo, Yangyun Zou, Aashish N. Adhikari, Steven E. Brenner

    出版 2023
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    Artigo
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  3. 3
    <i>Vibrio cholerae</i> biofilm growth program and architecture revealed by single-cell live imaging

    <i>Vibrio cholerae</i> biofilm growth program and architecture revealed by single-cell live imaging 由 Jing Yan, Andrew G. Sharo, Howard A. Stone, Ned S. Wingreen, Bonnie L. Bassler

    出版 2016
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    Artigo
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    Opportunities and challenges for the computational interpretation of rare variation in clinically important genes

    Opportunities and challenges for the computational interpretation of rare variation in clinically important genes 由 Gregory McInnes, Andrew G. Sharo, Megan L. Koleske, Julia E. H. Brown, Matthew Norstad, Aashish N. Adhikari, Sheng Wang, Steven E. Brenner, Jodi Halpern, Barbara A. Koenig, David Magnus, Renata C. Gallagher, Kathleen M. Giacomini, Russ B. Altman

    出版 2021
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    Revisão
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    Application of full-genome analysis to diagnose rare monogenic disorders

    Application of full-genome analysis to diagnose rare monogenic disorders 由 Joseph T.C. Shieh, Monica Penon‐Portmann, K. Wong, Michal Levy‐Sakin, Michelle Verghese, Anne Slavotinek, Renata C. Gallagher, Bryce A. Mendelsohn, Jessica Tenney, Daniah Beleford, Hazel Perry, Stephen K. Chow, Andrew G. Sharo, Steven E. Brenner, Zhongxia Qi, Jingwei Yu, Ophir D. Klein, David I. K. Martin, Pui‐Yan Kwok, Dario Boffelli

    出版 2021
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    Artigo
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