Hypothesis Prioritisation in multi-trait Colocalization (HyPrColoc).
Genome-wide association studies (GWAS) have identified thousands of genomic regions affecting complex diseases. The next challenge is to elucidate the causal genes and mechanisms involved. One approach is to use statistical colocalization to assess shared genetic aetiology across multiple related traits (e.g. molecular traits, metabolic pathways and complex diseases) to identify causal pathways, prioritize causal variants and evaluate pleiotropy.
HyPrColoc is an efficient deterministic Bayesian divisive clustering algorithm using GWAS summary statistics that can detect colocalization across vast numbers of traits simultaneously.
Try replacing 3 above with previous package version:
# Note there is no "prior.c" parameter in this version, instead use "prior.2 = 1 - prior.c". Default settings are matched.
Otherwise, on a Windows machine try updating Rtools: remove the previous version of Rtools (probably located C:\Rtools) and download Rtools40 from CRAN [https://cran.r-project.org/bin/windows/Rtools/]
# Regression coefficients and standard errors from ten GWAS studies (Traits 1-5, 6-8 & 9-10 colocalize)
betas <- hyprcoloc::test.betas
head(betas)
ses <- hyprcoloc::test.ses
head(ses)
# Trait names and SNP IDs
traits <- paste0("T", 1:10)
rsid <- rownames(betas)
# Colocalization analysis
hyprcoloc(betas, ses, trait.names=traits, snp.id=rsid)