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. Author manuscript; available in PMC: 2021 Feb 25.
Published in final edited form as: Nat Genet. 2020 Mar 30;52(4):437–447. doi: 10.1038/s41588-020-0594-5

Extended Data Fig. 6 ∣. Out-of-sample prediction in PGC cohorts.

Extended Data Fig. 6 ∣

a, This figure shows the Nagelkerke’s r2 of polygenic risk scores (PRS) calculated for each definition of depression in UK Biobank and MDD status indicated in 19 PGC29-MDD cohorts, while controlling for cohort specific effects. PRS were calculated using effect sizes at independent (LD r2 < 0.1) SNPs passing P-value thresholds 10−4, 0.001, 0.01, 0.05, 0.01, 0.2, 0.5 and 1 respectively, in GWAS performed on all definitions of depression in UK Biobank. b, This figure shows the same analysis performed on down-sampled data (7,500 cases, 42,500 controls) for each definition of depression.