CNVrd2

DOI: 10.18129/B9.bioc.CNVrd2    

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

Bioconductor version: Release (3.15)

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 (version "4.2") and enter:

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("CNVrd2")

For older versions of R, please refer to the appropriate Bioconductor release.

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 1.34.0
In Bioconductor since BioC 2.13 (R-3.0) (9 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_1.34.0.tar.gz
Windows Binary CNVrd2_1.34.0.zip
macOS Binary (x86_64) CNVrd2_1.34.0.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 https://bioconductor.org/packages/CNVrd2/
Package Downloads Report Download Stats

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