Hi guys,
I am using picard collectrnaserqmetics and I am confused about some fundamental concept here:
picard will report the number of bases mapped to different genomic features including coding region, UTR, intron, intergenic region, and ribosome.
If I have reads mapped to a non-coding RNA, e.g., lincRNA, will the reads be attributed to which part of genomic feature?
Thank you.
I am using picard collectrnaserqmetics and I am confused about some fundamental concept here:
picard will report the number of bases mapped to different genomic features including coding region, UTR, intron, intergenic region, and ribosome.
If I have reads mapped to a non-coding RNA, e.g., lincRNA, will the reads be attributed to which part of genomic feature?
Thank you.