Package: variants
Title: Annotating Genomic Variants
Version: 1.0.2
Date: 2017-09-05
Authors@R: person(role="cre", "Bioconductor Package Maintainer", email = "maintainer@bioconductor.org")
Description: Read and write VCF files. Identify structural location of variants and compute amino acid coding changes for non-synonymous variants. Use SIFT and PolyPhen database packages to predict consequence of amino acid coding changes 
Depends: R (>= 3.3.0), VariantAnnotation, cgdv17, org.Hs.eg.db,
        TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome.Hsapiens.UCSC.hg19,
        PolyPhen.Hsapiens.dbSNP131
License: Artistic-2.0
Encoding: UTF-8
LazyData: true
VignetteBuilder: knitr
biocViews: VariantAnnotation, GenomicVariation
Suggests: knitr, rmarkdown
NeedsCompilation: no
URL: https://www.bioconductor.org/help/workflows/variants/
Packaged: 2017-10-04 18:20:21 UTC; SYSTEM
Author: Bioconductor Package Maintainer [cre]
Maintainer: Bioconductor Package Maintainer <maintainer@bioconductor.org>
Built: R 3.4.2; ; 2017-10-04 18:25:18 UTC; windows
