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本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

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AI 根据所提供的论文材料归类:摘要的处理内和跨处理相关筛选属于通用高维方法,未明确涉及时间滞后或经济网络机制,不据相关术语强行归类。

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代码、数据与补充材料

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关注这篇论文的作者
Alfred Hero
Bala Rajaratnam

大规模相关性筛选

研究问题
当变量数量远多于样本量时,如何筛出与其他变量高度相关的变量,并理解阈值降低引发的发现数骤增与假阳性风险?
方法与思路
作者研究单处理、跨处理及持续相关的阈值筛选,推导发现数均值和相变阈值,并在弱依赖条件下给出泊松支配结果。
材料陈述的贡献
摘要称,理论刻画了发现数、相变阈值和假阳性率,并有数值结果支持;基因表达应用展示了跨多个处理保持相关的变量。
阅读关注点
应核对高维渐近设定、弱依赖条件和假阳性的定义,区分筛选变量与估计相关参数,并确认泊松支配而非精确泊松分布。
阅读边界
仅据版本未注明的 OpenAlex 索引摘要。相变公式及适用条件未提供;此处自相关指处理内变量相关,不能据此推断时间序列结论或刊本变化。

原文摘要

This article addresses the problem of screening for variables with high correlations in high-dimensional data in which there can be many fewer samples than variables. We focus on threshold-based correlation screening methods for three related applications: screening for variables with large correlations within a single treatment (autocorrelation screening), screening for variables with large cross-correlations over two treatments (cross-correlation screening), and screening for variables that have persistently large autocorrelations over two treatments (persistent-correlation screening). The novelty of correlation screening is that it identifies a smaller number of variables that are highly correlated with others compared with identifying a number of correlation parameters. Correlation screening suffers from a phase transition phenomenon; as the correlation threshold decreases, the number of discoveries increases abruptly. We obtain asymptotic expressions for the mean number of discoveries and the phase transition thresholds as a function of the number of samples, the number of variables, and the joint sample distribution. We also show that under a weak dependency condition, the number of discoveries is dominated by a Poisson random variable giving an asymptotic expression for the false-positive rate. The correlation screening approach yields tremendous dividends in terms of the type and strength of the asymptotic results that can be obtained. It also overcomes some of the major hurdles faced by existing methods in the literature, because correlation screening is naturally scalable to high dimensions. Numerical results strongly validate the theory presented here. We illustrate the application of the correlation screening methodology on a large-scale gene-expression dataset, revealing a few influential variables that exhibit significant correlation over multiple treatments. This article has supplementary material online.

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