Open VincentGardeux opened 4 months ago
This goes along with the variant view we discussed already. I can write a script in R or Python to run the PheWAS across all phenotypes for a given variant, and preprocess everything?
Yes, let me know when it's ready
Or maybe call it "Variant", since it will be a variant-centric view? To be defined.
It would make a standard PheWAS plot, aggregating the p-values of a particular variant across all phenotypes. We should be able to search for a variant and get the GWAS results as a standard PheWAS plot
Ideally, the phenotypes should be sorted by category