Python toolkit for fast genotype I/O, ancestry analysis, population-genetics statistics, genotype QC, GWAS, and visualization
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Updated
Sep 10, 2026 - Python
Python toolkit for fast genotype I/O, ancestry analysis, population-genetics statistics, genotype QC, GWAS, and visualization
Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R
Dual-condition genotype imputation benchmark on 1000 Genomes chr20: is Beagle's DR2 calibrated, and does calibration survive an ancestry-mismatched reference panel? plink2 + Beagle 5.5 with abstention analysis, bootstrap CIs, and exact QC accounting.
Reference implementation of the bgen format. Adapted for maintainability from https://github.com/gavinband/bgen
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