####################################################################
## 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
####################################################################
#Function to plot copy numbers and/or pcf segmentation results for one given chromosome with a separate plot for each sample
#Input:
### data: dataframe or matrix with chromosomes in first column, positions in second column and copy number data for one or more samples in subsequent columns
### segments: a data frame or a list with data frames containing segmentation results
### pos.unit: the unit used to represent the positions in data
### sample: a numeric vector indicating which samples are to be plotted (numerated such that sample=1 indicates the first sample found in data)
### chrom: numeric/character vector giving the chromosomes to be plotted
### xaxis: what is to be plotted along xaxis; either positions ("pos") or indeces ("index")
### layout: the grid layout for the plot (number of columns and rows)
### plot.ideo: should ideogram be plotted below plots
### ... : other optional plot parameters
##Required by:
### none
##Requires:
### checkAndRetrievePlotInput
### chromMax
### framedim
### get.seglim
### getPlotParameters
### getFilename
### plotIdeogram
### plotObs
### plotSegments
plotChrom <- function(data=NULL,segments=NULL,pos.unit="bp",sample=NULL,chrom=NULL,assembly="hg19",winsoutliers=NULL,xaxis="pos",layout=c(1,1), plot.ideo=TRUE,...){
#Check, modify and retrieve plot input:
input <- checkAndRetrievePlotInput(data=data,segments=segments,winsoutliers=winsoutliers,type="chromosome",xaxis=xaxis,pos.unit=pos.unit,sample=sample,chrom=chrom)
data <- input$data
segments <- input$segments
sampleID <- input$sampleID
chrom <- input$chrom
winsoutliers <- input$winsoutliers
nSeg <- length(segments) #will be 0 if segments=NULL
nChrom <- length(chrom)
nSample <- length(sampleID)
sample.names <- colnames(data)[-c(1:2)] #will be NULL if data=NULL
#Plot layout
nr <- layout[1]
nc <- layout[2]
#If xaxis is index; cannot plot ideogram:
if(xaxis=="index"){
plot.ideo <- FALSE
}
#Set default plot parameters and change these if user has specified other choices via ... :
arg <- getPlotParameters(type="chromosome",cr=nc*nr,chrom=chrom,nSeg=nSeg,plot.ideo=plot.ideo,xaxis=xaxis,assembly=assembly,...)
#Check if there should be more than one file/window with plot(s), and get file.name accordingly
nPage <- ifelse(arg$onefile,1,nChrom)
file.name <- getFilename(nPage,arg$file.name,ID=paste("Chrom",chrom,sep=" "),type="chromosome")
#Outer argins used for the plot window:
if(arg$title[1]==""){
oma <- c(0,0,0,0)
}else{
oma <- c(0,0,1,0)
}
mar=c(0.2,0.2,0.3,0.2)
#Make it possible to plot more than one chromosome; each chromosomeplot will be in separate file/window:
for(c in 1:nChrom){
#Start new window/file:
if(!arg$onefile || c==1){
#Either print to file, or plot on screen
if(!is.null(arg$dir.print)){
pdf(file=paste(arg$dir.print,"/",file.name[c],".pdf",sep=""),width=arg$plot.size[1],height=arg$plot.size[2],onefile=TRUE,paper="a4") #a4-paper
}else{
if(dev.cur()<=c){ #to make Sweave work
dev.new(width=arg$plot.size[1],height=arg$plot.size[2],record=TRUE)
}
}
}else{
#Start new page when prompted by user:
if(is.null(arg$dir.print)){
devAskNewPage(ask = TRUE)
}
}
#Initialize
row=1
clm=1
new = FALSE
#Divide the plotting window by the function "framedim":
frames <- framedim(nr,nc)
#Which chromosome is this:
k <- chrom[c]
ind.chrom <- which(data[,1]==k) #will be integer(0) if data=NULL
#Get maximum position on chromosome from assembly info
xmax <- NULL
if(plot.ideo){
xmax <- chromMax(chrom=k,cyto.data=arg$assembly,pos.unit=arg$plot.unit)
}
#Get data ylimits for this chromosome using all sampleID (equalrange=TRUE)
if(!is.null(data) && arg$equalRange){
all.sample <- which(sample.names %in% sampleID)
data.lim <- quantile(data[ind.chrom,all.sample+2],probs=c(arg$q/2,(1-arg$q/2)),names=FALSE,type=4,na.rm=TRUE)
}
#Picking out all segments where chromosome number (in second column) is k, returns new list
if(!is.null(segments)){
chrom.segments <- lapply(segments,function(seg,k){seg[seg[,2]==k,]},k=k)
}
#Separate plots for each sample
for(i in 1:nSample){
#Since probe positions are the same across the samples, we only want to print warning about probe positons located outside the
#chromosome after the last sample has been plotted:
#Select relevant sample
id <- sampleID[i]
#Frame dimensions for this plot:
fig.c <- c(frames$left[clm],frames$right[clm],frames$bot[row],frames$top[row])
par(fig=fig.c,new=new,oma=oma,mar=mar)
frame.c <- list(left=frames$left[clm],right=frames$right[clm],bot=frames$bot[row],top=frames$top[row])
#Divide frame for this sample into a frame for the actual plot and a frame for the ideogram:
plot.frame <- frame.c
plot.frame$bot <- frame.c$bot + (frame.c$top-frame.c$bot)*arg$ideo.frac
ideo.frame <- frame.c
ideo.frame$top <- plot.frame$bot
#Get segment limits:
seg.lim <- NULL
if(!is.null(segments)){
#Get min and max values in segments to make sure all are shown in plot
seg.lim <- sapply(chrom.segments,get.seglim,equalRange=arg$equalRange,sampleID=sampleID) #matrix with limits for each segmentation for this chromosome, min in row 1, max in row2
seg.lim <- c(min(seg.lim[1,],na.rm=TRUE),max(seg.lim[2,],na.rm=TRUE)) #Get overall min and max over all segments
}
#Start plotting:
#PLOT IDEOGRAM
if(plot.ideo){
par(fig=unlist(ideo.frame),new=new,mar=arg$mar.i)
plotIdeogram(chrom=k,arg$cyto.text,cyto.data=arg$assembly,cex=arg$cex.cytotext,unit=arg$plot.unit)
new=TRUE
}
#PLOT DATA POINTS:
add = FALSE
if(!is.null(data)){
ind.sample <- which(sample.names==id)
if(!arg$equalRange){
#Get data limits this chromosome using only this sample (if equalRange=FALSE)
data.lim <- quantile(data[ind.chrom,ind.sample+2],probs=c(arg$q/2,(1-arg$q/2)),names=FALSE,type=4,na.rm=TRUE)
}
plotObs(y=data[ind.chrom,ind.sample+2],pos=data[ind.chrom,2],unit=pos.unit,winsoutliers=winsoutliers[ind.chrom,ind.sample+2],type="chromosome",xaxis=xaxis,
plot.ideo=plot.ideo,k=k,sampleID=id,frame=plot.frame,new=new,op=arg,data.lim=data.lim,seg.lim=seg.lim,xmax=xmax)
add = TRUE ##segment plot will be added on top of data plot
}else{
data.lim <- NULL
}
#Plot segments:
if(!is.null(segments)){
#Plot all segments in list:
for(s in 1:nSeg){
use.segments <- chrom.segments[[s]]
plotSegments(use.segments[use.segments[,1]==id,,drop=FALSE],type="chromosome",k=k,sampleID=id,xaxis=xaxis,add=add,plot.ideo=plot.ideo,col=arg$seg.col[s],
lty=arg$seg.lty[s],lwd=arg$seg.lwd[s],frame=plot.frame,new=new,unit=pos.unit,seg.lim=seg.lim,data.lim=data.lim,op=arg)
add=TRUE
}#endfor
#Add segmentation legends:
if(!is.null(arg$legend)){
legend("topright",legend=arg$legend,col=arg$seg.col,lty=arg$seg.lty,cex=arg$cex.axis)
}
}
#If page is full; plot on new page
if(i%%(nr*nc)==0){
#Add main title to window page:
title(arg$title[c],outer=TRUE)
#Start new window page when prompted by user:
if(is.null(arg$dir.print)){
devAskNewPage(ask = TRUE)
}
#Reset columns and row in layout:
clm = 1
row = 1
new=FALSE
}else{
#Update column and row index:
if(clm<nc){
clm <- clm+1
}else{
clm <- 1
row <- row+1
}#endif
new=TRUE
}#endif
}#endfor
#Add main title to page:
title(arg$title[c],outer=TRUE)
#Close graphcis:
if(!is.null(arg$dir.print)){
if(!arg$onefile){
cat("Plot was saved in ",paste(arg$dir.print,"/",file.name[c],".pdf",sep=""),"\n")
graphics.off()
}else{
if(c==nChrom){
cat("Plot was saved in ",paste(arg$dir.print,"/",file.name,".pdf",sep=""),"\n")
graphics.off()
}
}
}#endif
}#endfor
}#endfunction
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