Additional file 5: 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.8873873.v1

12864_2019_5863_MOESM5_ESM.docx (263.13 kB)

Additional file 5: 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 S5. A catalogue of all recurrent false positive variants identified among 1000 Genome, Omani and Indigenous Australian cohorts. (DOCX 263 kb)

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Single nucleotide variant Miscall Resampling Exome Alignment

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Additional file 5: of Recurrent miscalling of missense variation from short-read genome sequence data

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