Thank you for your suggestion! I did not know about DEX-Seq, I am running it now and will compare it with my previous results.
Maria
Hello,
I have RNA-seq data from paired samples and want to do isoform-level differential expression.
My understanding is that is not possible to explicitly specify paired design in cuffdiff, so I considered the option of using the isoforms.read_group_tracking file and extract the raw_frags column, which I think corresponds to counts. Then use this as input in edgeR where I can specify paired-sample design.
Does this sound sensible?
If not, my question is: which package can I use to do isoform-level DE which takes into consideration paired-sample designs.
Thanks,
Maria
DEX-Seq Estimates exon usage coefficients from the fitted terms of the GLM and may be just what you're looking for.
http://www.bioconductor.org/packages/release/bioc/manuals/DEXSeq/man/DEXSeq.pdf
Thank you for your suggestion! I did not know about DEX-Seq, I am running it now and will compare it with my previous results.
Maria
I have played sleuth. But if I am interested with DE genes but not DE transcripts in downstream analysis, how could I do it with sleuth?
e.g. I got the DE transcripts table with Q<0.05 with associated gene name. But as you know, one gene could have multiple transcripts.
like
target_id Q ext_gene
ENST00000257570 0 OASL
ENST00000339275 1.08823325997074e-138 OASL
ENST00000543677 4.50865532164411e-20 OASL
Could I use it for finding DE genes like edgeR/DESeq? how?
Thank you!
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