To install this package, start R and enter:

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

In most cases, you don't need to download the package archive at all.

exomeCopy

DOI: 10.18129/B9.bioc.exomeCopy

Copy number variant detection from exome sequencing read depth

Bioconductor version: Release (3.5)

Detection of copy number variants (CNV) from exome sequencing samples, including unpaired samples. The package implements a hidden Markov model which uses positional covariates, such as background read depth and GC-content, to simultaneously normalize and segment the samples into regions of constant copy count.

Author: Michael Love

Maintainer: Michael Love <michaelisaiahlove at gmail.com>

Citation (from within R, enter citation("exomeCopy")):

Installation

To install this package, start R and enter:

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

Documentation

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

browseVignettes("exomeCopy")
PDF R Script Copy number variant detection in exome sequencing data
PDF Reference Manual
Text NEWS

Details

Version 1.22.0
In Bioconductor since BioC 2.9 (R-2.14) (6 years)
License GPL (>= 2)
Depends IRanges(>= 2.5.27), GenomicRanges(>= 1.23.16), Rsamtools
Imports stats4, methods, GenomeInfoDb
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Package Archives

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

Source Package exomeCopy_1.22.0.tar.gz
Windows Binary exomeCopy_1.22.0.zip (32- & 64-bit)
Mac OS X 10.11 (El Capitan) exomeCopy_1.22.0.tgz
Source Repository git clone https://git.bioconductor.org/packages/exomeCopy
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