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####################################################################
## Author: Gro Nilsen, Knut Liestřl and Ole Christian Lingjćrde.
## Maintainer: Gro Nilsen <gronilse@ifi.uio.no>
## License: Artistic 2.0
## Part of the copynumber package
## Reference: Nilsen and Liestřl et al. (2012), BMC Genomics
####################################################################
# Function that separates chromosomes in genome-plots by color
## Required by:
## plotFreq (genomeFreq)
## Requires:
## getArmandChromStop
## convert.unit
chromPattern <- function(pos.unit,op) {
#Use cytoband data information to get stopping points of chromosomes:
chromstop <- getArmandChromStop(op$assembly,pos.unit)$chromstop
scale.fac <- convert.unit(unit1=op$plot.unit,unit2=pos.unit) #Scaling factor according to plot.unit
chrom.mark <- c(1,cumsum(chromstop))*scale.fac
#Drop chrom24 if no observations for this chrom in data/segments:
#if(!any(segments[,2]==24)){
# chrom.mark <- chrom.mark[-length(chrom.mark)]
#}
#Let background be black to avoid white parts in arms without probes:
#rect(par("usr")[1], par("usr")[3], par("usr")[2], par("usr")[4], col = "white")
for (i in 1:(length(chrom.mark)-1)) {
if(i%%2==0){
rect(chrom.mark[i], par("usr")[3], chrom.mark[i+1], par("usr")[4], col = "grey95")#, border=NA)
}
}
}
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