Bioconductor version: Release (2.12)
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 | 1.6.0 | 
| 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_1.6.0.tar.gz | 
| Windows Binary | CNAnorm_1.6.0.zip (32- & 64-bit) | 
| Mac OS X 10.6 (Snow Leopard) | CNAnorm_1.6.0.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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