Hi,
I am using RunGSEAPreranked and getting some errors called successful with some errors. I am using list of preranked genes with fold change. I am not getting list of pathways with enrichment score and p values.
Second question, how to determine which gene set and chip platform to use for our research questions where we wanted to discover the list of genes and pathways associated with chemical exposure in cord blood RSeq data.
Thank you and looking forward to your valuable suggestions.
Best regards,
Parwez