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Fig. 1 | Genome Medicine

Fig. 1

From: Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

Fig. 1

Study design and imputation pipelines. The study design has four groups: a pipeline validation data set and b technical concordance cohort, diverse ancestry data set, and clinical cohort. The imputation pipeline for each group is depicted. hcWGS, high coverage whole genome sequencing; lcWGS, low coverage whole genome sequencing; HWE, Hardy-Weinberg equilibrium; GPS, genome-wide polygenic score; CAD, coronary artery disease; BC, breast cancer; AF, atrial fibrillation

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