Article
Vcflib and tools for processing the VCF variant call format
2021-05-23
Abstract excerpt
Since its introduction in 2011 the variant call format (VCF) has been widely adopted for processing DNA and RNA variants in practically all population studies — as well as in somatic and germline mutation studies. VCF can present single nucleotide variants, multi-nucleotide variants, insertions and deletions, and simple structural variants called against a reference genome. Here we present over 125 useful and much...
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Identifiers and source
- Literature Corpus work
- 7f411440-448d-56d5-bb83-f104e38bd150
- DOI
- 10.1101/2021.05.21.445151