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本文引用的文献

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Robust estimation of the false discovery rate.错误发现率的稳健估计
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Outlier sums for differential gene expression analysis.差异基因表达分析的异常值总和
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Multidimensional local false discovery rate for microarray studies.微阵列研究的多维局部错误发现率
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Tuberin is a component of lipid rafts and mediates caveolin-1 localization: role of TSC2 in post-Golgi transport.结节性硬化蛋白是脂筏的一个组成部分,并介导小窝蛋白-1的定位:TSC2在高尔基体后运输中的作用。
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用于基因组数据异常值检测的离散非参数算法。

Discrete nonparametric algorithms for outlier detection with genomic data.

作者信息

Ghosh Debashis

机构信息

Department of Statistics, Penn State University, University Park, Pennsylvania, USA.

出版信息

J Biopharm Stat. 2010 Mar;20(2):193-208. doi: 10.1080/10543400903572704.

DOI:10.1080/10543400903572704
PMID:20309754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2845329/
Abstract

In high-throughput studies involving genetic data such as from gene expression microarrays, differential expression analysis between two or more experimental conditions has been a very common analytical task. Much of the resulting literature on multiple comparisons has paid relatively little attention to the choice of test statistic. In this article, we focus on the issue of choice of test statistic based on a special pattern of differential expression. The approach here is based on recasting multiple-comparison procedures for assessing outlying expression values. A major complication is that the resulting p values are discrete; some theoretical properties of sequential testing procedures in this context are explored. We propose the use of q value estimation procedures in this setting. Data from a gene expression profiling experiment in prostate cancer are used to illustrate the methodology.

摘要

在涉及基因数据(如基因表达微阵列数据)的高通量研究中,两个或多个实验条件之间的差异表达分析一直是一项非常常见的分析任务。关于多重比较的大量相关文献相对较少关注检验统计量的选择。在本文中,我们基于一种特殊的差异表达模式,聚焦于检验统计量的选择问题。这里的方法基于重新构建用于评估异常表达值的多重比较程序。一个主要的复杂情况是由此产生的p值是离散的;本文探讨了在此背景下序贯检验程序的一些理论性质。我们建议在这种情况下使用q值估计程序。来自前列腺癌基因表达谱实验的数据用于说明该方法。