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Chunk #55 — Methods — Defining the study-wide significant cut-offs for collapsing analyses

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Rare variant contribution to human disease in 281,104 UK Biobank exomes.
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Bonferroni correction for multiple testing was inappropriate to use in this study given the high degree of correlation among the studied phenotypes and the level of similarity among the multiple collapsing models. Thus, we took two approaches to define more appropriate study-wide significance thresholds for the gene-based collapsing PheWAS.