Authors:
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, RE Handsaker, G Lunter, GT Marth, ST Sherry, G McVean, R Durbin, 1000 Genomes Project Analysis Group
Journal name: 
Bioinformatics
Citation info: 
27(15):2156-2158
Abstract: 
SUMMARY: The variant call format (VCF) is a generic format for storing DNA polymorphism data such as SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is usually stored in a compressed manner and can be indexed for fast data retrieval of variants from a range of positions on the reference genome. The format was developed for the 1000 Genomes Project, and has also been adopted by other projects such as UK10K, dbSNP and the NHLBI Exome Project. VCFtools is a software suite that implements various utilities for processing VCF files, including validation, merging, comparing and also provides a general Perl API. AVAILABILITY: http://vcftools.sourceforge.net
DOI: 
http://doi.org/10.1093/bioinformatics/btr330
Research group: 
Marioni Group
E-pub date: 
01 Aug 2011