Hi everyone,
I have a problem to represent my RNAseq data. I have a list of DE genes as output of DEseq2. So I would like to make an heatmap of these genes across all my conditions (3 conditions, and 3 samples per condition)
Problems starts here because I don't really know which values I have to take in input of DEseq2. Can I sort my DE gene-list and perform my heatmap with the values provided by the rlog function of DEseq2?
Sorry for the naive question, maybe i'm totally wrong. Thanks
Dear Nicolas, Hi
Please have a look at this Trinity page for "Automatically Partitioning Genes into Expression Clusters" and "Interactive analysis of DE features using MeV".
Maybe that could help.
~ Best
Hello :) Thanks for the answer, I will have a look on it. Best ;)