具有高维协变量的惩罚性变量选择的错误发现控制。

IF 0.9 4区 数学 Q3 Mathematics
Kevin He, Xiang Zhou, Hui Jiang, Xiaoquan Wen, Yi Li
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引用次数: 0

摘要

现代生物技术产生了大量的高通量数据,预测因子的数量远远超过了样本量。惩罚性变量选择已成为一种强大而高效的降维工具。然而,在惩罚性高维变量选择中控制错误发现(即包含无关变量)是一项严峻的挑战。为了有效控制惩罚性变量选择的错误发现率,我们提出了一种错误发现控制程序。所提出的方法具有通用性和灵活性,可用于多种变量选择算法,不仅适用于线性回归,还适用于广义线性模型和生存分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

False discovery control for penalized variable selections with high-dimensional covariates.

False discovery control for penalized variable selections with high-dimensional covariates.

False discovery control for penalized variable selections with high-dimensional covariates.

False discovery control for penalized variable selections with high-dimensional covariates.

Modern bio-technologies have produced a vast amount of high-throughput data with the number of predictors much exceeding the sample size. Penalized variable selection has emerged as a powerful and efficient dimension reduction tool. However, control of false discoveries (i.e. inclusion of irrelevant variables) for penalized high-dimensional variable selection presents serious challenges. To effectively control the fraction of false discoveries for penalized variable selections, we propose a false discovery controlling procedure. The proposed method is general and flexible, and can work with a broad class of variable selection algorithms, not only for linear regressions, but also for generalized linear models and survival analysis.

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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
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