Tests for differentiation in gene expression using a data-driven order or weights for hypotheses

被引:17
|
作者
Hommel, G [1 ]
Kropf, S
机构
[1] Johannes Gutenberg Univ Mainz, Inst Med Biomet Epidemiol & Informat, D-6500 Mainz, Germany
[2] Univ Magdeburg, Inst Biomet & Med Informat, D-39106 Magdeburg, Germany
关键词
multiple tests; closure test; familywise error rate; data-driven order for hypotheses; data-driven weights for hypotheses; gene expression;
D O I
10.1002/bimj.200410118
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the analysis of gene expression by microarrays there are usually few subjects, but high-dimensional data. By means of techniques, such as the theory of spherical tests or with suitable permutation tests, it is possible to sort the endpoints or to give weights to them according to specific criteria determined by the data while controlling the multiple type I error rate. The procedures developed so far are based on a sequential analysis of weighted p-values (corresponding to the endpoints), including the most extreme situation of weighting leading to a complete order of p-values. When the data for the endpoints have approximately equal variances, these procedures show good power properties. In this paper, we consider an alternative procedure, which is based on completely sorting the endpoints, but smoothed in the sense that some perturbations in the sequence of the p-values are allowed. The procedure is relatively easy to perform, but has high power under the same restrictions as for the weight-based procedures.
引用
收藏
页码:554 / 562
页数:9
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