StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants
2022 · The American Journal of Human Genetics · 68 citations
https://doi.org/10.1016/j.ajhg.2021.12.007
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Andrew G. Sharo
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Andrew G. Sharo is an academic researcher from University of California, Santa Cruz. The author has contributed to research in topics: Genomics and Rare Diseases & Cancer Genomics and Diagnostics & Genomic variations and chromosomal abnormalities. The author has an h-index of 7, co-authored 22 publications.
ORCID: 0000-0001-6533-8385Papers by this author
worksApplication of full-genome analysis to diagnose rare monogenic disorders
2021 · npj Genomic Medicine · 52 citations
https://doi.org/10.1038/s41525-021-00241-5
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
2023 · Genome Medicine · 43 citations
https://doi.org/10.1186/s13073-023-01199-y
Additional file 1 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23682195
Additional file 9 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23682219
Additional file 2 of ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23682198
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