Hi Everyone, I am trying to go from a bam file to a bedgraph file where I have fixed intervals of 100bp.
chr1 0 100 4
chr1 100 200 5
chr1 200 300 6
...
I have used genomeCoverageBed to compute the coverage, but can I use it to output counts in fixed window sizes of 100bp?? I would like to use that because it has scaling option and that would make one less step downstream.
If not what can I use to include scaling factor and fixed window size? igvtools count?? or deeptools??
Thanks