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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