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A Comparison of Methods to Control Type I Errors in Microarray Studies

Chen Jinsong, J. van der Laan Mark, Smith Martyn T. and Hubbard Alan E.
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Chen Jinsong: Lawrence Berkeley National Laboratory
J. van der Laan Mark: University of California, Berkeley
Smith Martyn T.: University of California, Berkeley
Hubbard Alan E.: University of California, Berkeley

Statistical Applications in Genetics and Molecular Biology, 2007, vol. 6, issue 1, 1-19

Abstract: Microarray studies often need to simultaneously examine thousands of genes to determine which are differentially expressed. One main challenge in those studies is to find suitable multiple testing procedures that provide accurate control of the error rates of interest and meanwhile are most powerful, that is, they return the longest list of truly interesting genes among competitors. Many multiple testing methods have been developed recently for microarray data analysis, especially resampling based methods, such as permutation methods, the null-centered and scaled bootstrap (NCSB) method, and the quantile-transformed-bootstrap-distribution (QTBD) method. Each of these methods has its own merits and limitations. Theoretically permutation methods can fail to provide accurate control of Type I errors when the so-called subset pivotality condition is violated. The NCSB method does not suffer from that limitation, but an impractical number of bootstrap samples are often needed to get proper control of Type I errors. The newly developed QTBD method has the virtues of providing accurate control of Type I errors under few restrictions. However, the relative practical performance of the above three types of multiple testing methods remains unresolved. This paper compares the above three resampling based methods according to the control of family wise error rates (FWER) through data simulations. Results show that among the three resampling based methods, the QTBD method provides relatively accurate and powerful control in more general circumstances.

Date: 2007
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DOI: 10.2202/1544-6115.1310

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