hypRcoloc with 1500 phenotypes across 200 loci
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More of a question than an issue, but here we go:
I have run hypRcoloc on a dataset with ~1500 phenotypes measured on the same individuals. There are ~200 loci where at least 1 phenotype has genome-wide significant P-value < 5e-8. To make computations easier (/not crash my PC), for each loci, I extracted all phenotype with at least a suggestive P-value < 1e-6 and ran hypRcoloc with default parameters.
Results look pretty good, but I'm wondering about the priors: In the preprint, you run hyprcoloc in predefined LD-blocks. In my case, I run hypRcoloc at loci where I know at least one phenotype has significant signal.
Should I change prior.1 or prior.2 to something other than defaults in this case?
Hi Malte,
I think the default priors should be okay in your situation. @cnfoley anything to add here?
Best wishes,
James