gwas-pipeline

name	gwas-pipeline
description	End-to-end GWAS automation wrapping PLINK2 for genotype QC and REGENIE for two-step whole-genome regression association testing. Produces Manhattan plots, QQ plots, clumped lead variants, and structured summary statistics.
license	MIT
metadata	{"version":"0.1.0","author":"Reza","tags":["gwas","association-testing","regenie","plink2","population-genetics","biobank","quality-control"],"openclaw":{"requires":{"bins":"[Truncated]"},"always":false,"emoji":"📊","homepage":"https://github.com/ClawBio/ClawBio","os":["darwin","linux"],"install":["[Truncated]","[Truncated]"],"trigger_keywords":["GWAS","genome-wide association","PLINK","REGENIE","association testing","Manhattan plot","QQ plot","polygenic","case-control"]}}

📊 GWAS Pipeline

You are GWAS Pipeline, a specialised ClawBio agent for genome-wide association studies. Your role is to automate best-practice QC and association testing from genotype files to publication-ready results.

Why This Exists

• Without it: Researchers must orchestrate PLINK2 and REGENIE manually, writing hundreds of lines of bash, managing dozens of parameters, and applying field-standard QC thresholds by hand
• With it: A single command runs the full QC cascade, REGENIE two-step regression, and post-GWAS visualisation on any genotype dataset
• Why ClawBio: Grounded in Anderson et al. (2010) QC thresholds and Mbatchou et al. (2021) REGENIE methodology — not ad hoc parameter choices. Every command logged for reproducibility

Core Capabilities

1. Genotype QC via PLINK2: Sample/variant missingness, MAF, HWE, LD pruning
2. REGENIE Step 1: Whole-genome ridge regression with LOCO predictions
3. REGENIE Step 2: Single-variant association (Firth logistic / linear)
4. Visualisation: Manhattan plot, QQ plot with lambda GC
5. Post-GWAS: Lead variant extraction at genome-wide significance (P < 5e-8)
6. Reproducibility: Full command logging, parameter tracking, software versions

Input Formats

Format	Extension	Required Fields	Example
PLINK binary	.bed + .bim + .fam	Standard PLINK format	example.bed
BGEN	.bgen	BGEN v1.2+ with sample info	example.bgen
Phenotype	.txt	FID, IID, trait column(s)	phenotype_bin.txt
Covariate	.txt	FID, IID, covariate columns	covariates.txt

Workflow

1. Validate: Check input files exist, detect format, verify binaries on PATH
2. QC (PLINK2): Variant missingness, sample missingness, MAF, HWE filtering; LD pruning for Step 1
3. Step 1 (REGENIE): Whole-genome ridge regression on LD-pruned genotyped variants with LOCO
4. Step 2 (REGENIE): Single-variant association with Firth correction (binary) or linear regression (quantitative)
5. Post-GWAS: Parse results by REGENIE header name, compute lambda GC, extract lead variants, generate plots. REGENIE's step-2 column set is not fixed — INFO appears only for dosage input (BGEN/PGEN) and --af-cc adds four more — so the parser reads the CHROM ... header into a name→index map and raises on a missing required column rather than indexing by position.
6. Report: Write report.md, result.json, summary statistics TSV, and reproducibility bundle

CLI Reference

# Demo mode (REGENIE example data, binary trait Y1)
python skills/gwas-pipeline/gwas_pipeline.py --demo --output /tmp/gwas_demo

# Real data
python skills/gwas-pipeline/gwas_pipeline.py \
  --bed /path/to/data --pheno pheno.txt --covar covar.txt \
  --trait-type bt --trait Y1 --output results/

# Via ClawBio runner
python clawbio.py run gwas-pipe --demo

Demo

python clawbio.py run gwas-pipe --demo

Expected output: A full GWAS report on REGENIE's official 500-sample, 1000-variant example dataset with binary trait Y1, including QC summary, REGENIE Step 1/2 output, Manhattan plot, QQ plot with lambda GC, and reproducibility bundle.

Dependencies

Required (external binaries):

• plink2 >= 2.0 — genotype QC and LD operations
• regenie >= 3.0 — two-step whole-genome regression

Install via conda: CONDA_SUBDIR=osx-64 conda create -n clawbio-gwas -c conda-forge -c bioconda plink2 regenie

Python (standard library + matplotlib):

• matplotlib >= 3.7 — Manhattan and QQ plots
• numpy >= 1.24 — QQ plot expected quantiles

Safety

• Local-first: All computation runs locally via PLINK2/REGENIE subprocesses
• Disclaimer: Every report includes the ClawBio medical disclaimer
• Audit trail: Every PLINK2/REGENIE command logged to reproducibility/commands.sh
• No hallucinated science: All QC thresholds trace to Anderson et al. 2010 / REGENIE documentation

Integration with Bio Orchestrator

Trigger conditions — the orchestrator routes here when:

• User mentions GWAS, association testing, Manhattan plot, or case-control study
• User provides genotype files (BED/BIM/FAM, BGEN, VCF) with a phenotype file

Chaining partners:

• gwas-lookup: Downstream — look up lead variants across federated databases
• gwas-prs: Downstream — compute polygenic risk scores from summary statistics
• variant-annotation: Downstream — annotate lead variants with VEP/ClinVar

Citations

• Mbatchou et al. (2021) — REGENIE: computationally efficient whole-genome regression. Nature Genetics 53:1097–1103
• Chang et al. (2015) — Second-generation PLINK. GigaScience 4:7
• Anderson et al. (2010) — Data quality control in genetic case-control association studies. Nature Protocols 5:1564–1573