Multiple testing with false discovery rate (FDR) control has been widely conducted in the "discrete paradigm" where p-values have discrete and heterogeneous null distributions with finitely many discontinuities. However, existing FDR procedures may lose some power when applied to such p-values. We propose a weighted FDR procedure for multiple testing in the discrete paradigm that efficiently adapts to both the heterogeneity and discreteness of p-value distributions. We prove the conservativeness of the weighted FDR procedure and demonstrate that it is more powerful than several other procedures for multiple testing based on p-values of binomial test or Fisher's exact test. The weighted FDR procedure is applied to a drug safety study and a differential methylation study based on discrete data, where it makes more discoveries than the Benjamini-Hochberg procedure at the same FDR level.
翻译:使用假发现率(FDR)控制的多重测试已在“分解范式”中广泛进行,在“分解范式中,p-value ” 中, p-value 具有离散和混杂的全无分布,且不完全不连续;然而,现有的FDR 程序在应用到这种p-value时可能会失去一些力量;我们提议在离散范式中,采用加权FDR 程序进行多重测试,以有效适应p-value 分布的异异性和离异性;我们证明加权FDR 程序的稳妥性,并证明它比其他若干基于二成体测试或Fisherer精确测试的多种程序更强大。加权FDR 程序适用于药物安全研究和基于离散数据的不同甲基化研究,其发现率高于同一FDR级的Benjani-Hochberg程序。