Significance analysis by minimizing false discovery rate

Yuanzhe Bei, Pengyu Hong
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引用次数: 1

Abstract

False discovery rate (FDR) control is widely practiced to correct for multiple comparisons in selecting statistically significant features from genome-wide datasets. In this paper, we present an advanced significance analysis method called miFDR that minimizes FDR when the number of the required significant features is fixed. We compared our approach with other well-known significance analysis approaches such as Significance Analysis of Microarrays [1-3], the Benjamini-Hochberg approach [4] and the Storey approach [5]. The results of using both simulated data sets and public microarray data sets demonstrated that miFDR is more powerful.
最小化错误发现率的显著性分析
错误发现率(FDR)控制被广泛应用于从全基因组数据集中选择统计显著特征的多重比较。在本文中,我们提出了一种称为miFDR的高级显著性分析方法,当所需显著特征的数量固定时,该方法可以最小化FDR。我们将我们的方法与其他著名的显著性分析方法进行了比较,如微阵列显著性分析[1-3]、Benjamini-Hochberg方法[4]和Storey方法[5]。使用模拟数据集和公共微阵列数据集的结果表明,miFDR更强大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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