Controlling FDR in selecting group-level simultaneous signals from multiple data sources with application to the National Covid Collaborative Cohort data
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One challenge in exploratory association studies using observational data is that the signals are potentially weak and the features have complex correlation structures. False discovery rate (FDR) controlling procedures can provide important statistical guarantees for replicability in risk factor identification in exploratory research. In the recently established National COVID Collaborative Cohort (N3C), electronic health record (EHR) data on the same set of candidate features are independently collected in multiple different sites, offering opportunities to identify signals by combining information from different sources. This paper presents a general knockoff-based variable selection algorithm to identify mutual signals from unions of group-level conditional independence tests with exact FDR control guarantees under finite sample settings. This algorithm can work with general regression settings, allowing heterogeneity of both the predictors and the outcomes across multiple data sources. We demonstrate the performance of this method with extensive numerical studies and an application to the N3C data.
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