Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Jul 15;30(14):2076-8.
doi: 10.1093/bioinformatics/btu168. Epub 2014 Mar 28.

VariantAnnotation: a Bioconductor package for exploration and annotation of genetic variants

Affiliations

VariantAnnotation: a Bioconductor package for exploration and annotation of genetic variants

Valerie Obenchain et al. Bioinformatics. .

Abstract

VariantAnnotation is an R / Bioconductor package for the exploration and annotation of genetic variants. Capabilities exist for reading, writing and filtering variant call format (VCF) files. VariantAnnotation allows ready access to additional R / Bioconductor facilities for advanced statistical analysis, data transformation, visualization and integration with diverse genomic resources.

Availability and implementation: This package is implemented in R and available for download at the Bioconductor Web site (http://bioconductor.org/packages/2.13/bioc/html/VariantAnnotation.html). The package contains extensive help pages for individual functions and a 'vignette' outlining typical work flows; it is made available under the open source 'Artistic-2.0' license. Version 1.9.38 was used in this article.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Danecek P, et al. The variant call format and VCFtools. Bioinformatics. 2011;27:2156–2158. - PMC - PubMed
    1. Drmanac R, Sparks AB. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science. 2010;327:78–81. - PubMed
    1. Gentleman RC, et al. Bioconductor: open software development for computational biology and bioinformatics. Genome Biol. 2004;5:R80. - PMC - PubMed
    1. Heng L. Tabix: fast retrieval of sequence features from generic TAB-delimited files. Bioinformatics. 2010;27:718–719. - PMC - PubMed
    1. Koboldt D, et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res. 2012;22:568–576. - PMC - PubMed

Publication types