bio-causal-genomics-colocalization-analysis
byfreedomintelligence· 44 skills
Test whether two traits share a causal variant at a genomic locus using Bayesian colocalization with coloc. Computes posterior probabilities for shared vs distinct causal variants between GWAS and eQTL signals. Use when determining if a GWAS signal and an eQTL share the same causal variant.
How to install bio-causal-genomics-colocalization-analysis?
freedomintelligence/openclaw-medical-skills/bio-causal-genomics-colocalization-analysis
$npx -y skills add freedomintelligence/openclaw-medical-skills --skill bio-causal-genomics-colocalization-analysisInstalls into the current project.
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Run `npx skills use "https://github.com/freedomintelligence/openclaw-medical-skills" --skill "freedomintelligence/openclaw-medical-skills/bio-causal-genomics-colocalization-analysis"` and follow the generated skill instructions now. Read its complete output, redirecting it to a temporary file first if necessary. Resolve relative paths from the supporting-files directory it provides.
Use the skills in "https://github.com/freedomintelligence/openclaw-medical-skills" that are relevant to the current task. Run `npx skills add "https://github.com/freedomintelligence/openclaw-medical-skills"` and select the relevant skills, then follow their instructions.
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