We are in the process of trying to get to grips with some eQTL analysis. I have a intuition that we should be correcting for unknown population structure, but I don't seem to be able to find guides for how to do it. I'm sure this also means there are other consdierations we are missing.
Does anyone know of a good best practices guide/tutorial/review for eQTL: not just how to operate the software (which the vignettes are generally good), but what statical considerations and pit-falls to look out for?
One pitfall I can mention is reads mapping to pseudogenes better than genes - if in one genome the gene is different than the reference and the reads are more similar to a pseudogene you will end up with reads mapped to a different location.