End-to-end GWAS workflow from VCF to association results. Covers PLINK QC, population structure correction, and association testing for case-control or quantitative traits. Use when running genome-wide association studies.
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name
bio-workflows-gwas-pipeline
description
End-to-end GWAS workflow from VCF to association results. Covers PLINK QC, population structure correction, and association testing for case-control or quantitative traits. Use when running genome-wide association studies.
Complete workflow for genome-wide association studies from genotype data to significant associations.
Workflow Overview
VCF/PLINK files
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[1. QC Filtering] ------> Sample and variant QC
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[2. LD Pruning] --------> Independent variants for PCA
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[3. Population Structure] --> PCA for covariates
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[4. Association Testing] --> Logistic/linear regression
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[5. Results] -----------> Manhattan plot, QQ plot
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Significant associations
Step 1: Data Import and QC
Convert VCF to PLINK
# VCF to PLINK binary format
plink2 --vcf input.vcf.gz \
--make-bed \
--out study
# Or with phenotype/covariate files
plink2 --vcf input.vcf.gz \
--pheno phenotypes.txt \
--make-bed \
--out study
Sample QC
# Calculate sample statistics
plink2 --bfile study \
--missing \
--out study_stats
# Remove samples with high missing rate (>5%)
plink2 --bfile study \
--mind 0.05 \
--make-bed \
--out study_sample_qc
# Check for sex discrepancies (if sex chromosome data available)
plink2 --bfile study_sample_qc \
--check-sex \
--out study_sex_check
# Remove related individuals (optional, requires IBD)
plink2 --bfile study_sample_qc \
--king-cutoff 0.0884 \
--make-bed \
--out study_unrelated