CNVrd2

DOI: 10.18129/B9.bioc.CNVrd2    

This package is for version 3.7 of Bioconductor; for the stable, up-to-date release version, see CNVrd2.

CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.

Bioconductor version: 3.7

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")):

Installation

To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("CNVrd2")

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("CNVrd2")

 

PDF R Script A Markdown Vignette with knitr
PDF   Reference Manual

Details

biocViews Clustering., CopyNumberVariation, Coverage, LinkageDisequilibrium, SNP, Sequencing, Software
Version 1.18.0
In Bioconductor since BioC 2.13 (R-3.0) (5 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
Links To Me
Build Report  

Package Archives

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

Source Package CNVrd2_1.18.0.tar.gz
Windows Binary CNVrd2_1.18.0.zip
Mac OS X 10.11 (El Capitan) CNVrd2_1.18.0.tgz
Source Repository git clone https://git.bioconductor.org/packages/CNVrd2
Source Repository (Developer Access) git clone git@git.bioconductor.org:packages/CNVrd2
Package Short Url http://bioconductor.org/packages/CNVrd2/
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