The variant call format and VCFtools
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...
Paper Details
Title
The variant call format and VCFtools
Published Date
Jun 7, 2011
Journal
Volume
27
Issue
15
Pages
2156 - 2158
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