## get read counts for given genomic windows
getWinCounts <- function(files, wins,
filetype = c("bed", "bam", "GRanges")
) {
if((!is.data.frame(wins)) & is(wins)[1]!="GRanges")
stop("Input genomic intervals must be a GRanges or data frame!")
if(is.data.frame(wins)) wins = import(wins)
counts = matrix(0, nrow = length(wins), ncol = length(files))
for(i in seq_len(length(files))) {
if(filetype!= "GRanges"){
if(filetype == "bam")
reads = read.BAM(files[i])
else if(filetype == "bed")
reads = import(files[i])
}else if(filetype == "GRanges"){
### data in datasetTRES package
reads = get(files[i])
}
#### ended
counts[,i] = countOverlaps(wins,reads)
}
colnames(counts) = files
counts
}
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