Optimal sample size for multiple testing: The case of gene expression microarrays

• 成果类型: Article
• 署名作者: Müller, P; Parmigiani, G; Robert, C; Rousseau, J
• 署名单位: University of Texas System; UTMD Anderson Cancer Center; Johns Hopkins University; Universite PSL; Universite Paris-Dauphine; Institut Polytechnique de Paris; ENSAE Paris; Universite Paris Cite
• 刊物名称: JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION
• ISSN/ISSBN: 0162-1459
• DOI: 10.1198/016214504000001646
• 发表日期: 2004
• 页码: 990-1001
• 关键词: normalization; DESIGN; issues

摘要

We consider the choice of an optimal sample size for multiple-comparison problems. The motivating application is the choice of the number of microarray experiments to be carried out when learning about differential gene expression. However, the approach is valid in any application that involves multiple comparisons in a large number of hypothesis tests. We discuss two decision problems in the context of this setup: the. sample size selection and the decision about the multiple comparisons. We adopt a decision-theoretic approach, using loss functions that combine the competing goals of discovering as many differentially expressed genes as possible, while keeping the number of false discoveries manageable. For consistency, we use the same loss function for both decisions. The decision rule that emerges for the multiple-comparison problem takes the exact form of the rules proposed in the recent literature to control the posterior expected false-discovery rate. For the sample size selection, we combine the expected utility argument with an additional sensitivity analysis, reporting the conditional expected utilities and conditioning on assumed levels of the true differential expression. We recognize the resulting diagnostic as a form of statistical power facilitating interpretation and communication. As a sampling model for observed gene expression densities across genes and arrays, we use a variation of a hierarchical gamma/gamma model. But the discussion of the decision problem is independent of the chosen probability model. The approach is valid for any model that includes positive prior probabilities for the null hypotheses in the multiple comparisons and that allows for efficient marginal and posterior simulation, possibly by dependent Markov chain Monte Carlo simulation.