Robust Distance Correlation for Variable Screening.

Stat Pub Date : 2025-09-01 Epub Date: 2025-08-22 DOI:10.1002/sta4.70094
Tianzhou Ma, Fan Yang, Hongjie Ke, Zhao Ren
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Abstract

In modern statistical applications, identifying critical features in high-dimensional data is essential for scientific discoveries. Traditional best subset selection methods face computational challenges, while regularization approaches such as Lasso, SCAD and their variants often exhibit poor performance with ultrahigh-dimensional data. Sure screening methods, widely used for dimensionality reduction, have been developed as popular alternatives, but few target heavy-tailed characteristics in modern big data. This paper introduces a new sure screening method, based on robust distance correlation ('RDC'), designed for heavy-tailed data. The proposed method inherits the benefits of the original model-free distance correlation-based screening while robustly estimating distance correlation in the presence of heavy-tailed data. We further develop an FDR control procedure by incorporating the Reflection via Data Splitting (REDS) method. Extensive simulations demonstrate the method's advantage over existing screening procedures under different scenarios of heavy-tailedness. Its application to high-dimensional heavy-tailed RNA-seq data from The Cancer Genome Atlas (TCGA) pancreatic cancer cohort showcases superior performance in identifying biologically meaningful genes predictive of MAPK1 protein expression critical to pancreatic cancer.

变量筛选的鲁棒距离相关。
在现代统计应用中,识别高维数据中的关键特征对科学发现至关重要。传统的最佳子集选择方法面临计算挑战,而正则化方法如Lasso、SCAD及其变体在超高维数据中往往表现出较差的性能。确定筛选方法广泛用于降维,已成为流行的替代方法,但很少针对现代大数据中的重尾特征。本文介绍了一种基于鲁棒距离相关(RDC)的重尾数据可靠筛选方法。该方法继承了原始的基于无模型距离相关筛选的优点,同时在存在重尾数据的情况下稳健地估计距离相关。我们进一步发展了FDR控制程序,并结合了数据分割反射(REDS)方法。大量的模拟表明,在不同的重尾情况下,该方法优于现有的筛选程序。将其应用于癌症基因组图谱(TCGA)胰腺癌队列的高维重尾RNA-seq数据显示,在识别对胰腺癌至关重要的MAPK1蛋白表达具有生物学意义的预测基因方面具有卓越的性能。
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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