Bioconductor version: Release (2.11)
Performs ratio, GC content correction and normalization of data obtained using low coverage (one read every 100-10,000 bp) high troughput sequencing. It performs a "discrete" normalization looking for the ploidy of the genome. It will also provide tumour content if at least two ploidy states can be found.
Author: Stefano Berri <s.berri at leeds.ac.uk>, Henry M. Wood <H.M.Wood at leeds.ac.uk>, Arief Gusnanto <a.gusnanto at leeds.ac.uk>
Maintainer: Stefano Berri <s.berri at leeds.ac.uk>
To install this package, start R and enter:
source("http://bioconductor.org/biocLite.R") biocLite("CNAnorm")
To cite this package in a publication, start R and enter:
citation("CNAnorm")
CNAnorm.pdf | ||
Reference Manual | ||
Text | NEWS |
biocViews | Bioinformatics, Cancer, CopyNumberVariants, HighThroughputSequencing, Lung, Sequencing, Software |
Version | 1.4.0 |
In Bioconductor since | BioC 2.9 (R-2.14) |
License | GPL-2 |
Depends | R (>= 2.10.1), DNAcopy, methods |
Imports | methods |
Suggests | |
System Requirements | |
URL | http://www.r-project.org, |
Depends On Me | |
Imports Me | |
Suggests Me |
Package Source | CNAnorm_1.4.0.tar.gz |
Windows Binary | CNAnorm_1.4.0.zip (32- & 64-bit) |
MacOS 10.5 (Leopard) | CNAnorm_1.4.0.tgz |
Package Downloads Report | Download Stats |
Common Bioconductor workflows include:
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