Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data

Suyash S. Shringarpure, Rasika A. Mathias, Ryan D. Hernandez, Timothy D. O'Connor, Zachary A. Szpiech, Raul Torres, Francisco M. De La Vega, Carlos D. Bustamante, Kathleen C. Barnes, Margaret A. Taub

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