####################################################################
## Author: Gro Nilsen, Knut Liestøl and Ole Christian Lingjærde.
## Maintainer: Gro Nilsen <gronilse@ifi.uio.no>
## License: Artistic 2.0
## Part of the copynumber package
## Reference: Nilsen and Liestøl et al. (2012), BMC Genomics
####################################################################
#Get the maximum position on a given chromosome
#Input:
### chrom: number between 1-24 indicating which chromosome's ideogram is to be plotted
### cyto.data: data frame with cytoband-information
### unit: the unit used for positions in the plot
### cyto.unit: the unit used to represent positons in cyto.data
# Output:
### max.pos: a scalar giving the maximum position on this chromosome (given the cytoband information)
##Required by:
### plotFreq (chromosomeFreq)
### plotAllele
### plotChrom
### plotSample
### plotHeatmap
### plotWeightedFreq
## Requires:
### convert.unit
chromMax <- function(chrom,cyto.data,pos.unit,cyto.unit="bp"){
#Get scaling factor for positions
s <- convert.unit(unit1=pos.unit,unit2=cyto.unit)
#Get the rows in cytoband data that correspond to this chromosome
if(chrom==23){
txt <- "chrX"
}else if(chrom==24){
txt <- "chrY"
}else{
txt <- paste("chr",chrom,sep="")
}
rows <- which(cyto.data[,1]==txt)
##Get max position for this chromosome and scale according to pos.unit
max.pos <- max(cyto.data[rows,3])
max.pos <- max.pos*s
return(max.pos)
}
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