So Devon, In other words if I am not using DEseq/EdgeR or Limma we work with read counts without nay further normalization?
microrna-seq normalization in differential expression
I have raw counts of miroRNA seq. Do we normalize read count before we apply any t test/ DESEq? I believe we dont need length normlaization
Thanks
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DESeq2/edgeR/limma (via voom) have their own normalization mechanisms. There's no need to do length normalization, the length of a given miRNA is the same between your groups.
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To be frank, if you're asking this question then you don't know enough to correctly analyze this type of data without a pre-made R package like DESeq2/edgeR/limma. If you continue this with some method you're coming up with then the results will very likely be wrong.
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