Hello,
I am analyzing RNA-Seq profile. I am surprized that the profile is not regular along the gene (up and down, some regions lots of reads, some a few). For each gene, the profile is the same between different replicates. When I compared between 2 conditions, I found interesting differences, which may have biological meanings, in RNA degradation. I was in auto-scale. Then I changed in log-scale (after an advice of bioinformatician), I could not see the differences anymore, so I was a little dissapointed.
So I would like to know log-scale or auto-scale, which is more precise and when we use each one, what are the differences?
Thank you a lot for your help.
Huong nguyen