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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 to covert local posistions to global positions based on a defined set of local stop positions chromosomes given in cyto.data
##Input:
### chromosomes: vector with chromosome numbers
### position: vector with positions
### pos.unit: positon's unit
### cyto.data: data frame with cytoband information
### delta: number of base pairs to add to end of each chromosome (used by plotCircle)
##Output:
### glob.pos: vector with global positions
##Required by:
### adjustSeg
### getx
### plotCircle
##Requires:
### getArmandChromStop
getGlobPos <- function(chromosomes, position, pos.unit, cyto.data, delta=0){
#Get local stopping posistions for each p-arm and each chromosome from cytoband data
l <- getArmandChromStop(cyto.data=cyto.data,unit=pos.unit)
chromstop <- l$chromstop
#Need to make sure that none of the input positions are larger than chromosome stop postions:
u.chrom <- unique(chromosomes)
new.pos <- position
for(j in 1:length(u.chrom)){
probe.c <- chromosomes==u.chrom[j]
#Check for positions that are larger than chromosome max position
out <- which(position[probe.c] > chromstop[u.chrom[j]])
#Replace these positions by max chrom position:
new.pos[probe.c][out] <- chromstop[u.chrom[j]]
}
chromstop <- chromstop + delta
glob.chromstop <- cumsum(chromstop) #Global stopping position for each chromosome
glob.pos <- new.pos + c(0,glob.chromstop[-length(glob.chromstop)])[chromosomes] #Calculate global positions by adding global chromstop (for chrom > 1, for chrom=1 positions remain unchanged
return(glob.pos)
}#end getGlobPos
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