bio-workflows-causal-genomics-pipeline

Triangulate causal evidence from GWAS summary statistics using Mendelian randomization and sensitivity analyses.

Updated Aug 27, 2026
One-click install
npx skills add https://github.com/stellaromics/fast-bioinfo --skill bio-workflows-causal-genomics-pipeline
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: bio-workflows-causal-genomics-pipeline
Source: https://github.com/stellaromics/fast-bioinfo/tree/main/.claude/agents/spatial-analysis/skills/bio-workflows-causal-genomics-pipeline
Command: npx skills add https://github.com/stellaromics/fast-bioinfo --skill bio-workflows-causal-genomics-pipeline

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

End-to-end post-GWAS causal inference pipeline that connects GWAS summary statistics to causal effects, enabling researchers to identify exposures, shared variants, and mediating mechanisms through a structured, reproducible workflow.

Core Features & Use Cases

  • Instrument selection and Mendelian randomization analysis (IVW, MR-Egger, weighted median) to triangulate causal effects.
  • Comprehensive sensitivity analyses (MR-PRESSO, Egger intercept, Steiger directionality) to assess pleiotropy and bias.
  • Colocalization and fine-mapping to pinpoint shared causal variants at loci of interest.
  • Mediation analysis via multivariable MR to evaluate indirect pathways and mediators.
  • End-to-end workflow examples for typical post-GWAS questions (e.g., BMI and cardiovascular outcomes).

Quick Start

Run the full causal inference pipeline on your GWAS summary statistics to obtain triangulated causal evidence.

Frequently Asked Questions about bio-workflows-causal-genomics-pipeline

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I perform Mendelian randomization and sensitivity analysis on GWAS summary statistics?

Apply Mendelian randomization to GWAS summary statistics using IVW, MR-Egger, and weighted median methods, then validate results with MR-PRESSO, Egger intercept, and Steiger directionality tests to assess pleiotropy and bias.

Can I run colocalization and fine-mapping to identify shared causal variants from GWAS data?

Run colocalization and fine-mapping on GWAS summary statistics using coloc and susieR to pinpoint shared causal variants at loci of interest, generating robust evidence for shared genetic architecture.

Do I need R and specific packages like TwoSampleMR to run this causal inference pipeline?

You need R installed with key packages including TwoSampleMR, MR-PRESSO, coloc, susieR, and MendelianRandomization, plus access to full summary statistics to produce reproducible causal inference results.

What is the best way to conduct mediation analysis for post-GWAS causal inference?

Conduct mediation analysis for post-GWAS causal inference via multivariable MR to evaluate indirect pathways and identify mediators, applying a structured end-to-end workflow for common post-GWAS questions.

How does instrument selection work in a Mendelian randomization workflow?

Instrument selection in a Mendelian randomization workflow identifies genetic variants strongly associated with the exposure from GWAS summary statistics, serving as proxies to estimate causal effects on outcomes.

When should I use triangulation for causal evidence linking exposures to outcomes?

Use triangulation for causal evidence when you need to integrate multiple methods like Mendelian randomization, colocalization, and sensitivity analyses to robustly confirm that an exposure causally affects an outcome.