Hi! Thanks for this tool. I have a lot of reads that align to intergenic regions. I was wondering if there is there a way that I can subset these reads for further analysis?
Unfortunately, RNA-SeQC does not offer a way to subset reads like that, but you should be able to use bedtools to filter your bam to only include intergenic reads
Hi! Thanks for this tool. I have a lot of reads that align to intergenic regions. I was wondering if there is there a way that I can subset these reads for further analysis?
Thanks!