Quick calculation for sample size while controlling false discovery rate with application to microarray analysis

被引:92
作者
Liu, Peng [1 ]
Hwang, J. T. Gene
机构
[1] Cornell Univ, Dept Biol Stat & Computat Biol, Ithaca, NY 14853 USA
[2] Iowa State Univ Sci & Technol, Dept Stat, Ames, IA 50011 USA
[3] Cornell Univ, Dept Math, Ithaca, NY 14853 USA
[4] Cornell Univ, Dept Stat Sci, Ithaca, NY 14853 USA
[5] Natl Cheng Kung Univ, Dept Stat, Tainan 70101, Taiwan
关键词
D O I
10.1093/bioinformatics/btl664
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Sample size calculation is important in experimental design and is even more so in microarray or proteomic experiments since only a few repetitions can be afforded. In the multiple testing problems involving these experiments, it is more powerful and more reasonable to control false discovery rate (FDR) or positive FDR (pFDR) instead of type I error, e.g. family-wise error rate (FWER). When controlling FDR, the traditional approach of estimating sample size by controlling type I error is no longer applicable. Results: Our proposed method applies to controlling FDR. The sample size calculation is straightforward and requires minimal computation, as illustrated with two sample t-tests and F-tests. Based on simulation with the resultant sample size, the power is shown to be achievable by the q-value procedure.
引用
收藏
页码:739 / 746
页数:8
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