To install this package, start R and enter:
## try http if https is not available source("https://bioconductor.org/biocLite.R") biocLite("CNVrd2")
In most cases, you don't need to download the package archive at all.
Bioconductor version: Release (3.1)
CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples, indentify SNPs tagging copy number variants and detect copy number polymorphic genomic regions.
Author: Hoang Tan Nguyen, Tony R Merriman and Mik Black
Maintainer: Hoang Tan Nguyen <hoangtannguyenvn at gmail.com>
Citation (from within R,
enter citation("CNVrd2")
):
To install this package, start R and enter:
## try http if https is not available source("https://bioconductor.org/biocLite.R") biocLite("CNVrd2")
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("CNVrd2")
R Script | A Markdown Vignette with knitr | |
Reference Manual |
biocViews | Clustering., CopyNumberVariation, Coverage, LinkageDisequilibrium, SNP, Sequencing, Software |
Version | 1.6.0 |
In Bioconductor since | BioC 2.13 (R-3.0) (2 years) |
License | GPL-2 |
Depends | R (>= 3.0.0), methods, VariantAnnotation, parallel, rjags, ggplot2, gridExtra |
Imports | DNAcopy, IRanges, Rsamtools |
LinkingTo | |
Suggests | knitr |
SystemRequirements | |
Enhances | |
URL | https://github.com/hoangtn/CNVrd2 |
Depends On Me | |
Imports Me | |
Suggests Me | |
Build Report |
Follow Installation instructions to use this package in your R session.
Package Source | CNVrd2_1.6.0.tar.gz |
Windows Binary | CNVrd2_1.6.0.zip |
Mac OS X 10.6 (Snow Leopard) | CNVrd2_1.6.0.tgz |
Mac OS X 10.9 (Mavericks) | CNVrd2_1.6.0.tgz |
Subversion source | (username/password: readonly) |
Git source | https://github.com/Bioconductor-mirror/CNVrd2/tree/release-3.1 |
Package Short Url | http://bioconductor.org/packages/CNVrd2/ |
Package Downloads Report | Download Stats |
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