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This package is for version 3.3 of Bioconductor; for the stable, up-to-date release version, see exomeCopy.
Bioconductor version: 3.3
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")
):
To install this package, start R and enter:
## try http:// if https:// URLs are not supported source("https://bioconductor.org/biocLite.R") biocLite("exomeCopy")
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("exomeCopy")
R Script | Copy number variant detection in exome sequencing data | |
Reference Manual | ||
Text | NEWS |
biocViews | CopyNumberVariation, Genetics, Sequencing, Software |
Version | 1.18.0 |
In Bioconductor since | BioC 2.9 (R-2.14) (5 years) |
License | GPL (>= 2) |
Depends | IRanges(>= 2.5.27), GenomicRanges(>= 1.23.16), Rsamtools |
Imports | stats4, methods, GenomeInfoDb |
LinkingTo | |
Suggests | Biostrings |
SystemRequirements | |
Enhances | |
URL | |
Depends On Me | |
Imports Me | CNVPanelizer, contiBAIT, Rariant, SomaticCancerAlterations |
Suggests Me | |
Build Report |
Follow Installation instructions to use this package in your R session.
Package Source | exomeCopy_1.18.0.tar.gz |
Windows Binary | exomeCopy_1.18.0.zip (32- & 64-bit) |
Mac OS X 10.9 (Mavericks) | exomeCopy_1.18.0.tgz |
Subversion source | (username/password: readonly) |
Git source | https://github.com/Bioconductor-mirror/exomeCopy/tree/release-3.3 |
Package Short Url | http://bioconductor.org/packages/exomeCopy/ |
Package Downloads Report | Download Stats |
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