Oxford University Press / Wellcome Trust / Genomes Project Analysis Group / Creative Commons / /
Country
United States / United Kingdom / / /
Facility
University of Oxford / Boston College / National Human Genome Research Institute / Wellcome Trust Genome Campus / BGZF library / National Library of Medicine / Wellcome Trust Sanger Institute / University of Michigan / Broad Institute of MIT / /
Department of Biostatistics / National Human Genome Research Institute / National Institute of Health / Wellcome Trust Sanger Institute / University of Michigan / Ann Arbor / Wellcome Trust Centre for Human Genetics / Center for Statistical Genetics / MIT / Harvard / British Heart Foundation / Department of Statistics / Department of Biology / Boston College / National Institutes of Health National Center for Biotechnology Information / Broad Institute / Oxford University / Medical Research Council / University of Oxford / /
Person
Petr Danecek / Mark A. DePristo / Stephen T. Sherry / John Quackenbush / Gabor Marth / Robert Handsaker / Adam Auton / /
Position
Author / Editor / /
ProgrammingLanguage
Perl / C++ / /
ProvinceOrState
Maryland / Massachusetts / Michigan / /
Technology
Bioinformatics / Biotechnology / API / DNA sequencing / SNP / Perl / random access / genotype / human genome / /
Bioinformatics Advance Access published June 7, 2011 The Variant Call Format and VCFtools Petr Danecek 1,∗, Adam Auton 2,∗, Goncalo Abecasis 3 , Cornelis A. Albers 1 , Eric Banks 4 , Mark A. DePristo 4 , Robert Hand