This package is for version 3.8 of Bioconductor; for the stable, up-to-date release version, see seqCNA.
Bioconductor version: 3.8
Copy number analysis of high-throughput sequencing cancer data with fast summarization, extensive filtering and improved normalization
Author: David Mosen-Ansorena
Maintainer: David Mosen-Ansorena <dmosen.gn at cicbiogune.es>
Citation (from within R,
enter citation("seqCNA")
):
To install this package, start R (version "3.5") and enter:
if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("seqCNA")
For older versions of R, please refer to the appropriate Bioconductor release.
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("seqCNA")
R Script | seqCNA.pdf | |
Reference Manual |
biocViews | CopyNumberVariation, Genetics, Sequencing, Software |
Version | 1.28.0 |
In Bioconductor since | BioC 2.13 (R-3.0) (5.5 years) |
License | GPL-3 |
Depends | R (>= 3.0), GLAD(>= 2.14), doSNOW (>= 1.0.5), adehabitatLT (>= 0.3.4), seqCNA.annot(>= 0.99), methods |
Imports | |
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SystemRequirements | samtools |
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Build Report |
Follow Installation instructions to use this package in your R session.
Source Package | seqCNA_1.28.0.tar.gz |
Windows Binary | seqCNA_1.28.0.zip |
Mac OS X 10.11 (El Capitan) | seqCNA_1.28.0.tgz |
Source Repository | git clone https://git.bioconductor.org/packages/seqCNA |
Source Repository (Developer Access) | git clone git@git.bioconductor.org:packages/seqCNA |
Package Short Url | http://bioconductor.org/packages/seqCNA/ |
Package Downloads Report | Download Stats |
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