Hi,
Upon performing differential expression analysis for my RNA seq data set using DESeq I found that the log2 transformed differential expression values that I get from DESeq are very close to the RT-qPCR values but opposite in sign. I am new in the field and was concerned so as to why this would be happening? Is this something inherent to the way DESeq calculates the diff. values?
Thanks.
Have you tried to swap the "reference" transcriptome? Like you did AxB, if you do BxA, maybe?
Hi,
Ya, I tried that and it would change the signs but was confused whether it was the right thing to do by swapping the reference as I wasn't sure if DESeq was comparing b to a or a to b.The following reply cleared that too. Thanks :)