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. Author manuscript; available in PMC: 2018 Apr 1.
Published in final edited form as: Genet Epidemiol. 2017 Jan 15;41(3):251–258. doi: 10.1002/gepi.22029

Table 2.

Generalization testing results from a set of analyses based on a HCHS/SOL GWAS as the discovery study, and GLGC GWAS as the follow-up study. For each selection rule we report the number of SNPs selected for follow-up testing, and the number of loci containing these SNPs. For combinations of selection rules and multiple testing adjustment method we report the number of generalized loci, and the number of generalized loci that did not contain any SNP with p-value< 5 × 10−8 in the GLGC GWAS.

Selection rule selected SNPs loci adjustment gen SNPs gen loci # loci not sig Willer
Selection rule 1 - one-sided 1,662 89 FDRg r-values 1,352 27 5
Selection rule 1 - two-sided 1,208 51 FDRg r-values 1,076 21 1
10−6 742 18 FDRg r-values 706 17 0
10−6 742 18 FWERg r-values 583 17 0
Selection rule 2 - one-sided 627 17 FWERg r-values 583 17 0
Selection rule 2 - two-sided 574 16 FWERg r-values 538 16 0
5 × 10−8 546 15 FWERg r-values 514 15 0