normalizing EXOM-seq read using DESeq2
Hi,
I have exom read aligned to hg38. I used featureCounts to quantify the reads. Therefore, I would like to normalize the reads in the different sample using DESeq2. May I know if there especial consideration that I should take before doing it.
I mean I did not find anything related to EXOM seq in the DESeq2 vignettes.
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