Dear all,
I want to do differential expression at transcript level using an RNA-seq dataset that consists of paired samples (patient 1 control/treatment, patient2 control/treatment, etc.).
I have not found methods other than Ballgown and DEXSeq that are able to handle paired designs. I have also tried the option of obtaining transcript counts and use them in edgeR. However I am concerned about the fact that edgeR is not particularly adapted to do analysis on transcript counts.
Does anyone has any advice on how to go on this problem? Or if there is a way to assess my results with the latter approach I described?
Many thanks,
Maria
2 answers
Perhaps not the solution you were looking for, but software like kallisto and Salmon (and others) generate estimates of raw counts per transcript. You could use those estimates in edgeR or DESeq2.
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written
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Sean Davis
If you go that route, Martin Morgan has provided code to read in kallisto output:
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written
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Sean Davis
The combination of kallisto and sleuth will allow you to do a transcript level analysis while taking into account your paired design.
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written
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Lior Pachter
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Adding on the answer of Sean Davis, both salmon and kallisto can perform bootstrapping to estimate the uncertainty of the transcript level abundances.
edgeRnow has functions (catchSalmonandcatchKallisto) to use these bootstraps to assign an overdispersion value to each trancript. Larger mapping uncertainty means higher overdispersion, so the mapping uncertainty is taken into account during the differential analysis. Having that said, edgeR is able to perform transcript level analysis, check its manual. I think these methods were introduced to edgeR a few years ago, but not when OP asked this question.