Hi everyone,
I have performed pathway analyses with the same filtered gene list using different gene sets. The next step is to identify overlapping enriched pathways in the outputs of the databases used, such as IPA, KEGG, Reactome (as I assume they might have different denominations). I'm curious to know if there is any smart way of doing this, or would I have to do this manually?
Thanks!
Thanks for this. You're right, computing the overlap wouldn't really help me.
Having a quick look at the SetRank algorithm on the other hand tells me that it would probably do what I wish to do. However, I want something that I can use on my already generated outputs (if possible). I will keep SetRank in mind for the future as it seems to be a good resource.