mendelian-randomisation

Community

Analyze genetic association using Mendelian Randomization

AuthorMubasherMohammed
Version1.0.0
Installs0

System Documentation

What problem does it solve?

This Skill simplifies and automates Mendelian Randomization analysis for causal inference, saving users the need to manually handle complex calculations and statistical diagnostics.

Core Features & Use Cases

  • Estimation Methods: Supports multiple Mendelian Randomization estimators (IVW, MR-Egger, weighted median/mode, full sensitivity analysis).
  • Causal Inference: Determines potential causal relationships between genetic markers and diseases/traits.
  • Use Case: A user wants to explore if a particular gene variant is associated with an increased risk of a certain disease. They would input their genetic and disease outcome data, and this skill would output the causal effect estimate along with sensitivity analysis.

Quick Start

Run Mendelian Randomization analysis for genetic association by inputting the genetic instrument file 'instruments.json' and specify the output directory 'output'.

Dependency Matrix

Required Modules

numpyscipymatplotlib

Components

scriptsreferencesassets

💻 Claude Code Installation

Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.

Please help me install this Skill:
Name: mendelian-randomisation
Download link: https://github.com/MubasherMohammed/opencode-BioInfo/archive/main.zip#mendelian-randomisation

Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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