Entering edit mode
11.1 years ago
Nicolas Rosewick
11k
Hi,
How can I know the position and the length of soft-clipped nucleotides in my aligned reads (I used bowtie2 in local mode but the idea will be the same for other aligner). So from the sam file.
I put a little picture to explain more easily :
Thanks
N.
I checked in SAM spec and indeed I have to filter by cigar flag. Thanks a lot