4.6 Article

Covariate Adaptive False Discovery Rate Control With Applications to Omics-Wide Multiple Testing

Journal

JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION
Volume 117, Issue 537, Pages 411-427

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/01621459.2020.1783273

Keywords

Covariates; EM-algorithm; False discovery rate; Multiple testing

Funding

  1. NSF [DMS-1811747]
  2. Mayo Clinic Center for Individualized Medicine

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This article introduces an FDR control procedure that can incorporate covariate information in large-scale inference problems. The proposed procedure is implemented using a fast algorithm and has been shown to have asymptotic validity even in cases of misspecified models and weakly dependent p-values. Extensive simulations demonstrate that the method improves upon existing approaches in terms of flexibility, robustness, power, and computational efficiency. The method is applied to omics datasets from genomics studies to identify features associated with clinical and biological phenotypes, and shows superiority, particularly in sparse signal scenarios.
Conventional multiple testing procedures often assume hypotheses for different features are exchangeable. However, in many scientific applications, additional covariate information regarding the patterns of signals and nulls are available. In this article, we introduce an FDR control procedure in large-scale inference problem that can incorporate covariate information. We develop a fast algorithm to implement the proposed procedure and prove its asymptotic validity even when the underlying likelihood ratio model is misspecified and the p-values are weakly dependent (e.g., strong mixing). Extensive simulations are conducted to study the finite sample performance of the proposed method and we demonstrate that the new approach improves over the state-of-the-art approaches by being flexible, robust, powerful, and computationally efficient. We finally apply the method to several omics datasets arising from genomics studies with the aim to identify omics features associated with some clinical and biological phenotypes. We show that the method is overall the most powerful among competing methods, especially when the signal is sparse. The proposed covariate adaptive multiple testing procedure is implemented in the R package CAMT. Supplementary materials for this article are available online.

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