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Additional file 1: of Identification of missing variants by combining multiple analytic pipelines

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posted on 2018-04-16, 05:00 authored by Yingxue Ren, Joseph Reddy, Cyril Pottier, Vivekananda Sarangi, Shulan Tian, Jason Sinnwell, Shannon McDonnell, Joanna Biernacka, Minerva Carrasquillo, Owen Ross, NilĂźfer Ertekin-Taner, Rosa Rademakers, Matthew Hudson, Liudmila Mainzer, Yan Asmann
Table S1. The genomic location and GC content of BWA-unique, Novo-unique and shared variants. (DOCX 14 kb)

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National Institutes of Health

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    BMC Bioinformatics

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    Missing variantsCombining multiple bioinformatics pipelinesRare variants

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