Does R packages like edgeR, limma, DESeq2 work with QuantSeq 3' RNAseq? I mean, has anybody used and published results based on QuantSeq data analyzed with edgeR, limma, DESeq2?
Is there a particular advantage of using quant seq for RNAseq. I could not find any specific advantage except that it is 3' based sequencing. Any help ot pointing to the information will be helpful.
1 answer
A few advantages would be:
-only 3' sequencing so therefore far less sequencing for the same expression quantification. As such the cost of sequencing is reduced, or you can multiplex more samples on the machine.
-less problematic for heavily degraded RNA
Obviously, you won't have alternative splicing/isoform usage, so it depends on what the aim of your research is. If you only care about expression levels, QuantSeq is fine (and definitely better than microarray).
Does R packages like edgeR, limma, DESeq2 work with QuantSeq 3' RNAseq?
Yes
I meant that is there any reference (e.g. scientific article and not markerting material) which supports this? Do the authors of edger, limma, or DESeq2 concur with this?
That question would probably be more appropriate for the Bioconductor support forum.
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