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CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
by
Gai, Xiaowu
,
Perin, Juan C
,
Murphy, Kevin
,
O'Hara, Ryan
,
D'arcy, Monica
,
Wenocur, Adam
,
Xie, Hongbo M
,
Rappaport, Eric F
,
Shaikh, Tamim H
,
White, Peter S
Published in
BMC bioinformatics
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Evaluating sequence data quality from the Swift Accel-Amplicon CFTR Panel
by
Leung, Marco L.
,
Watson, Deborah J.
,
Vaccaro, Courtney N.
,
Mafra, Fernanda
,
Wenocur, Adam
,
Wang, Tiancheng
,
Hakonarson, Hakon
,
Santani, Avni
Published in
Scientific data
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Interpretation of Maturity-Onset Diabetes of the Young Genetic Variants Based on American College of Medical Genetics and Genomics Criteria: Machine-Learning Model Development
by
Liu, Yichuan
,
Qu, Hui-Qi
,
Wenocur, Adam S
,
Qu, Jingchun
,
Chang, Xiao
,
Glessner, Joseph
,
Sleiman, Patrick
,
Tian, Lifeng
,
Hakonarson, Hakon
Published in
JMIR biomedical engineering
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