SNPlocs.Hsapiens.dbSNP142.GRCh37

DOI: 10.18129/B9.bioc.SNPlocs.Hsapiens.dbSNP142.GRCh37    

SNP locations for Homo sapiens (dbSNP Build 142)

Bioconductor version: Release (3.6)

SNP locations and alleles for Homo sapiens extracted from NCBI dbSNP Build 142. The source data files used for this package were created by NCBI on October 14, 2014, and contain SNPs mapped to reference genome GRCh37.p13. WARNING: Note that the GRCh37.p13 genome is a patched version of GRCh37 but the patch doesn't alter chromosomes 1-22, X, Y, MT. GRCh37 itself is the same as the hg19 genome from UCSC *except* for the mitochondrion chromosome. Therefore, the SNPs in this package can be "injected" in BSgenome.Hsapiens.UCSC.hg19 and they will land at the correct location but this injection will exclude chrM (i.e. nothing will be injected in that sequence).

Author: Herv\'e Pag\`es

Maintainer: Simon Coetzee <simon.coetzee at cshs.org>

Citation (from within R, enter citation("SNPlocs.Hsapiens.dbSNP142.GRCh37")):

Installation

To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("SNPlocs.Hsapiens.dbSNP142.GRCh37")

Documentation

PDF   Reference Manual

Details

biocViews AnnotationData, Genetics, Homo_sapiens
Version 0.99.5
License Artistic-2.0
Depends R (>= 2.10), IRanges, GenomeInfoDb, GenomicRanges, BSgenome(>= 1.25.6)
Imports methods, utils, IRanges, GenomeInfoDb, GenomicRanges, BSgenome
LinkingTo
Suggests Biostrings, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Hsapiens.UCSC.hg19.masked(>= 1.3.19)
SystemRequirements
Enhances
URL
Depends On Me
Imports Me
Suggests Me motifbreakR

Package Archives

Follow Installation instructions to use this package in your R session.

Source Package SNPlocs.Hsapiens.dbSNP142.GRCh37_0.99.5.tar.gz
Windows Binary
Mac OS X 10.11 (El Capitan)
Package Short Url http://bioconductor.org/packages/SNPlocs.Hsapiens.dbSNP142.GRCh37/
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