Bioconductor version: Release (2.12)
Annotate variants, compute amino acid coding changes, predict coding outcomes
Author: Valerie Obenchain, Martin Morgan, Michael Lawrence with contributions from Stephanie Gogarten.
Maintainer: Valerie Obenchain <vobencha at fhcrc.org>
To install this package, start R and enter:
    source("http://bioconductor.org/biocLite.R")
    biocLite("VariantAnnotation")
    To cite this package in a publication, start R and enter:
    citation("VariantAnnotation")
    | R Script | filterVcf Overview | |
| R Script | Introduction to VariantAnnotation | |
| Reference Manual | ||
| Text | NEWS | 
| biocViews | Annotation, DataImport, Genetics, HighThroughputSequencing, Homo_sapiens, SNP, Sequencing, Software | 
| Version | 1.6.8 | 
| In Bioconductor since | BioC 2.9 (R-2.14) | 
| License | Artistic-2.0 | 
| Depends | R (>= 2.8.0), methods, BiocGenerics, GenomicRanges(>= 1.11.29), Rsamtools(>= 1.11.26), IRanges(>= 1.17.4) | 
| Imports | methods, BiocGenerics, IRanges, Biostrings, Biobase, Rsamtools, AnnotationDbi(>= 1.17.11), zlibbioc, BSgenome, GenomicFeatures(>= 1.9.35), DBI, utils | 
| Suggests | RUnit, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, SNPlocs.Hsapiens.dbSNP.20110815, SNPlocs.Hsapiens.dbSNP.20101109, SIFT.Hsapiens.dbSNP132, PolyPhen.Hsapiens.dbSNP131, snpStats, ggplot2 | 
| System Requirements | |
| URL | |
| Depends On Me | cgdv17, ensemblVEP, PolyPhen.Hsapiens.dbSNP131, SIFT.Hsapiens.dbSNP132, VariantTools | 
| Imports Me | FunciSNP, ggbio, GGtools, gmapR, HTSeqGenie, R453Plus1Toolbox, VariantTools | 
| Suggests Me | GenomicRanges, gmapR, GWASTools | 
| Package Source | VariantAnnotation_1.6.8.tar.gz | 
| Windows Binary | VariantAnnotation_1.6.8.zip (32- & 64-bit) | 
| Mac OS X 10.6 (Snow Leopard) | VariantAnnotation_1.6.8.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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