Entering edit mode
8.4 years ago
simonjean434
▴
70
Hello,
I have a bed file with genomic ranges. I would like to use htseq to count reads from my bam file that mapped to these particular regions.
Could you please let me know how I can do that with htseq ?
Thanks J
Why not use bedtools instead?
or ( along with beddtools ) you could use featureCounts instead of htseq-count unless there are overlapping ambiguous regions.