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Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data
Shringarpure, Suyash S., Mathias, Rasika A., Hernandez, Ryan D., O’Connor, Timothy D., Szpiech, Zachary A., Torres, Raul, De La Vega, Francisco M., Bustamante, Carlos D., Barnes, Kathleen C., Taub, MaLangue:
english
Journal:
Bioinformatics
DOI:
10.1093/bioinformatics/btw786
Date:
December, 2016
Fichier:
PDF, 274 KB
english, 2016