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Inference on the Limiting False Discovery Rate and the P-value Threshold Parameter Assuming Weak Dependence between Gene Expression Levels within Subject

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  • Heller Glenn

    (Memorial Sloan-Kettering Cancer Center)

  • Qin Jing

    (National Institute of Allergy and Infectious Diseases)

Abstract

An objective of microarray data analysis is to identify gene expressions that are associated with a disease related outcome. For each gene, a test statistic is computed to determine if an association exists, and this statistic generates a marginal p-value. In an effort to pool this information across genes, a p-value density function is derived. The p-value density is modeled as a mixture of a uniform (0,1) density and a scaled ratio of normal densities derived from the asymptotic normality of the test statistic. The p-values are assumed to be weakly dependent and a quasi-likelihood is used to estimate the parameters in the mixture density. The quasi-likelihood and the weak dependence assumption enables estimation and asymptotic inference on the false discovery rate for a given rejection region, and its inverse, the p-value threshold parameter for a fixed false discovery rate. A false discovery rate analysis on a localized prostate cancer data set is used to illustrate the methodology. Simulations are performed to assess the performance of this methodology.

Suggested Citation

  • Heller Glenn & Qin Jing, 2007. "Inference on the Limiting False Discovery Rate and the P-value Threshold Parameter Assuming Weak Dependence between Gene Expression Levels within Subject," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 6(1), pages 1-24, May.
  • Handle: RePEc:bpj:sagmbi:v:6:y:2007:i:1:n:14
    DOI: 10.2202/1544-6115.1285
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    1. Unknown, 2010. "A Compilation of Smart Marketing Articles, January 2008–October 2010," EB Series 121655, Cornell University, Department of Applied Economics and Management.

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