A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar

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. The VCF format can represent single nucleotide variants, multi-nucleotide variants, inse...

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Detalles Bibliográficos
Autores principales: Garrison, Erik, Kronenberg, Zev N., Dawson, Eric T., Pedersen, Brent S., Prins, Pjotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286226/
https://www.ncbi.nlm.nih.gov/pubmed/35639788
http://dx.doi.org/10.1371/journal.pcbi.1009123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286226/
https://www.ncbi.nlm.nih.gov/pubmed/35639788
http://dx.doi.org/10.1371/journal.pcbi.1009123

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