Hi, everyone,
Needs some help here. I'm new in RNAseq. Just wondering is there a quick way to count how many reads have mapped to the exon-intron boundaries?
I have sorted bam file, exon bed file, intron bed file.
Thanks!
Needs some help here. I'm new in RNAseq. Just wondering is there a quick way to count how many reads have mapped to the exon-intron boundaries?
I have sorted bam file, exon bed file, intron bed file.
Thanks!
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