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cyvcf2: fast, flexible variant analysis with Python

MOTIVATION: Variant call format (VCF) files document the genetic variation observed after DNA sequencing, alignment and variant calling of a sample cohort. Given the complexity of the VCF format as well as the diverse variant annotations and genotype metadata, there is a need for fast, flexible meth...

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Publicat a:Bioinformatics
Autors principals: Pedersen, Brent S, Quinlan, Aaron R
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5870853/
https://ncbi.nlm.nih.gov/pubmed/28165109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx057
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