Many exploratory experiments such as DNA microarray or brain imaging require simultaneously comparisons of hundreds or thousands of hypotheses. Under such a setting, using the false discovery rate (FDR) as an overall Type I error is recommended (Benjamini and Hochberg in J. R. Stat. Soc. B 57:289-300, 1995). Many FDR controlling procedures have been proposed. However, when evaluating the performance of FDR-controlling procedures, researchers are often focused on the ability of procedures to control the FDR and to achieve high power. Meanwhile, under the multiple hypotheses, it may be also likely to commit a false nondiscovery or fail to claim a true non-significance. In addition, various experimental parameters such as the number of hypotheses, the proportion of the number of true null hypotheses to the number of hypotheses, the samples size and the correlation structure may affect the performance of FDR controlling procedures. The purpose of this paper is to illustrate the performance of some existing FDR controlling procedures in terms of four indices, i.e., the FDR, the false nondiscovery rate, the sensitivity and the specificity. Analytical results of these indices for the FDR controlling procedures are derived. Simulations are also performed to evaluate the performance of controlling procedures in terms of these indices under various experimental parameters. The result can be used to summarize as a guidance for practitioners to properly choose a FDR controlling procedure.
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