collate_bb_subclones | R Documentation |
Then logic is applied for classifying copy number aberrations into a series of classes. There are two main groups: Clonal (starting with c) and Subclonal (starting with s).
collate_bb_subclones( samplename, cndata, gender, outfile, ploidy = NA, exclude_sex_chroms = F )
samplename |
A String containing the samplename |
cndata |
A data.frame in Battenberg subclones format |
gender |
Specify either the string male or female |
outfile |
A String with the full path to where the output should be written |
ploidy |
An optional parameter that is used to call gains/losses against. If higher than the ploidy a segment is considered a gain, lower a loss. When left as NA the sample ploidy is used (Default NA). |
exclude_sex_chroms |
Optional parameter whether to exclude sex chromosomes (Default FALSE) |
A CNA can be: * HD : Homozygous deletion * LOH : Loss of heterozygosity * Amp : Amplification * Gain : Gain * NoCNV : Normal copy number without aberrations * Loss : Loss
The copy number segments, classification, weighted ploidy and samplename are saved to the specified output file
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