Hi Everyone,
I have nascent RNA-Seq (not spiked) data for multiple conditions and I want to perfom differential expression analysis in the intronic regions to capture nascent differences. After Qc and trimming, I used the STAR for alignment and HTSeq for counting in intronic regions.
I have 2 questions:
I am wandering if the default DESeq2 normalization method (median-of-ratios) is suitable for introns, as it assumes that gene expression is on average constant.
Is the respective pipeline suitable for intron DE?
Thank you in advance!