New to NGS data, currently analyzing small RNA seq data with emphasis on piRNAs, looking to eventually do differential expression analysis. I have my reads aligned, but now a little unsure of how best to go about getting total read counts for the areas of the genome I am interested in. I have ~500 genomic coordinates for regions of interest which should be areas of piRNA production.
I'm thinking of using bedtools to get a count of alignments which overlap with my ~500 regions. Is there a better way to do this? Suggestions and useful commands/parameters/programs very welcome.
Cheers
I'm thinking of using bedtools to get a count of alignments which overlap with my ~500 regions. Is there a better way to do this? Suggestions and useful commands/parameters/programs very welcome.
Cheers
Comment