Hi,
I am wondering if there is an easy way to use HTSeq (in particular HTSeq-count) to perform a read counts on gene introns rather than exons.
Do you have any hints?
Thanks a lot
Marco
You could just modify the GFF file to have the coordinates of the intron instead of the exons.
The new documentation (due to come online soon) will have more details on how you can write your own scripts for such specialized counting tasks.
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You could just modify the GFF file to have the coordinates of the intron instead of the exons.
The new documentation (due to come online soon) will have more details on how you can write your own scripts for such specialized counting tasks.