Additional file 2: of Recurrent miscalling of missense variation from short-read genome sequence data

Field, Matthew; Burgio, Gaetan; Chuah, Aaron; Shekaili, Jalila; Hassan, Batool; Sukaiti, Nashat; Foote, Simon; Cook, Matthew; Andrews, T.

doi:10.6084/m9.figshare.8873861.v1

12864_2019_5863_MOESM2_ESM.docx (21.6 kB)

Additional file 2: of Recurrent miscalling of missense variation from short-read genome sequence data

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posted on 2019-07-16, 05:00 authored by Matthew Field, Gaetan Burgio, Aaron Chuah, Jalila Shekaili, Batool Hassan, Nashat Sukaiti, Simon Foote, Matthew Cook, T. Andrews

Table S2. Near-paralogs of example human recurrent false positive variants. (DOCX 23 kb)

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Single nucleotide variant Miscall Resampling Exome Alignment

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Additional file 2: of Recurrent miscalling of missense variation from short-read genome sequence data

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