Andrew G. Sharo

Opportunities and Challenges for Interpreting Rare Variation in Clinically Important Genes

Steven E. Brenner, Gregory McInnes, Russ B. Altman, 2020 .

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

Steven E. Brenner, Zhiqiang Hu, Andrew G. Sharo, 2020, bioRxiv.

Vibrio cholerae biofilm growth program and architecture revealed by single-cell live imaging

Jing Yan, Bonnie L. Bassler, Howard A. Stone, 2016, Proceedings of the National Academy of Sciences.

DBDS Workshop in Biostatistics and in pervasive population

Andrew G. Sharo, S. Brenner, Zhiqiang Hu, 2022 .

Investigation of the causal etiology in a patient with T-B+NK+ immunodeficiency

Andrew G. Sharo, S. Brenner, W. Leonard, 2022, Frontiers in Immunology.

Application of full-genome analysis to diagnose rare monogenic disorders

Andrew G. Sharo, P. Kwok, S. Brenner, 2020, npj Genomic Medicine.

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

Andrew G. Sharo, S. Brenner, S. Sunyaev, 2020, bioRxiv.

ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden

Andrew G. Sharo, Aashish N. Adhikari, S. Brenner, 2022, Genome Medicine.

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

Andrew G. Sharo, Megan L. Koleske, Aashish N. Adhikari, 2021, American journal of human genetics.