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Mingya Long

Publications and source records attributed to Mingya Long.

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Principled Inference in Dense High-Dimensional Linear Models via Local Conditional Sparsity

High-dimensional inference methods often rely on coefficient sparsity, an assumption that can be restrictive when signals are dense but individually weak. In such settings, valid inference may still be possible if the covariates exhibit sparse conditional dependence. Motivated by this observation, we propose Neighborhood-Localized Nested Regression (NLNR), a framework for coordinatewise inference in high-dimensional linear models with potentially dense coefficients. The central idea is to localize inference for a target coefficient to a low-dimensional working regression determined by a Sparse Conditional Neighborhood (SCN) of the target covariate. Specifically, for a given covariate, we estimate its SCN through nodewise $\ell_1$-penalized regression and then fit a regression using only the target covariate and its estimated neighborhood. Under suitable regularity conditions, we establish consistency and asymptotic normality of the resulting estimator. Building on this inferential reduction principle, we further develop a thresholding-based screening procedure with theoretical guarantees and a boosting variant that augments the working model with additional response-relevant covariates to improve finite-sample performance. Extensive simulations and an application to the CCLE dataset demonstrate favorable empirical performance.

stat.ME

Functional knockoffs selection with applications to functional data analysis in high dimensions

The knockoffs is a recently proposed powerful framework that effectively controls the false discovery rate (FDR) for variable selection. However, none of the existing knockoff solutions are directly suited to handle multivariate or high-dimensional functional data, which has become increasingly prevalent in various scientific applications. In this paper, we propose a novel functional model-X knockoffs selection framework tailored to sparse high-dimensional functional models, and show that our proposal can achieve the effective FDR control for any sample size. Furthermore, we illustrate the proposed functional model-X knockoffs selection procedure along with the associated theoretical guarantees for both FDR control and asymptotic power using examples of commonly adopted functional linear additive regression models and the functional graphical model. In the construction of functional knockoffs, we integrate essential components including the correlation operator matrix, the Karhunen-Lo\`eve expansion, and semidefinite programming, and develop executable algorithms. We demonstrate the superiority of our proposed methods over the competitors through both extensive simulations and the analysis of two brain imaging datasets.

stat.ME

The Cauchy Combination Test under Arbitrary Dependence Structures

Aggregating multiple effects is often encountered in large-scale data analysis where the fraction of significant effects is generally small. Many existing methods cannot handle it effectively because of lack of computational accuracy for small p-values. The Cauchy combination test (abbreviated as CCT) ( J Am Statist Assoc, 2020, 115(529):393-402) is a powerful and computational effective test to aggregate individual $p$-values under arbitrary correlation structures. This work revisits CCT and shows three key contributions including that (i) the tail probability of CCT can be well approximated by a standard Cauchy distribution under much more relaxed conditions placed on individual p-values instead of the original test statistics; (ii) the relaxation conditions are shown to be satisfied for many popular copulas formulating bivariate distributions; (iii) the power of CCT is no less than that of the minimum-type test as the number of tests goes to infinity with some regular conditions. These results further broaden the theories and applications of CCT. The simulation results verify the theoretic results and the performance of CCT is further evaluated with data from a prostate cancer study.

stat.ME