I used Trinity to create a fasta file for my transcriptome, which I then mapped to the genome. Unfortunately, there are a lot of single exon reads in the BAM file which appear to just be junk. Does anyone know of a good way to filter these out? I can do it manually, but I really don't want to do that for a full BAM file.
Question: Filter single exon reads
20 months ago by
sloux • 0
University of Kentucky
sloux • 0 wrote:
ADD COMMENT • link •
Please log in to add an answer.
Powered by Biostar version 2.3.0
Traffic: 1257 users visited in the last hour