Entering edit mode
5.9 years ago
Florian BERNARD
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20
Hi everyone,
I am working on a RNA-seq dataset generated with direct-RNA sequencing technology and the reads are rather bad. Out of 170K reads, only 90K are overlapping with a feature (according to HTseq-count). I was wondering if there was an easy way to extract only those reads as the other ones do not really interest me ?
Thanks in advance !