Zachary A. Szpiech - researchr alias

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Viewing Publication 1 - 3 from 3

2017

Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing dataSuyash S. Shringarpure, Rasika A. Mathias, Ryan D. Hernandez, Timothy D. O'Connor, Zachary A. Szpiech. bioinformatics, 33(8):1147-1153, 2017. [doi]

GARLIC: Genomic Autozygosity Regions Likelihood-based Inference and ClassificationZachary A. Szpiech, Alexandra Blant, Trevor J. Pemberton. bioinformatics, 33(13):2059-2062, 2017. [doi]

2008

ADZE: a rarefaction approach for counting alleles private to combinations of populationsZachary A. Szpiech, Mattias Jakobsson, Noah A. Rosenberg. bioinformatics, 24(21):2498-2504, 2008. [doi]

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