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AI 根据所提供的论文材料归类:摘要研究高维协变量联合检验的通用计算方法,遗传关联应用未明确对应所列经济学模型或计量细分方向。

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关注这篇论文的作者
Yaowu Liu
Jun Xie

通过高斯近似高效准确计算 p 值:一种蒙特卡洛方法

研究问题
在协变量相关、响应非高斯且有效信号稀疏时,如何准确计算多种联合检验的 p 值,同时降低大量置换检验的计算成本?
方法与思路
作者提出基于蒙特卡洛方案的高斯近似,处理最小 p 值、高阶批判和 Berk–Jones 检验,并推导非渐近近似误差界。
材料陈述的贡献
摘要称,该方法比置换更高效且精度相近;误差界在协变量数远大于样本量时仍可能趋零,并以遗传数据模拟和实例比较。
阅读关注点
应核对高斯近似对象、相关结构估计与误差界条件,以及维数增长限制、蒙特卡洛误差和与置换比较时的精度与成本口径。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明,不能推断刊本变化;误差界的具体条件和性能数值未说明,不能认定所有高维场景均准确。

原文摘要

It is of fundamental interest in statistics to test the significance of a set of covariates. For example, in genome-wide association studies, a joint null hypothesis of no genetic effect is tested for a set of multiple genetic variants. The minimum p-value method, higher criticism, and Berk–Jones tests are particularly effective when the covariates with nonzero effects are sparse. However, the correlations among covariates and the nonGaussian distribution of the response pose a great challenge toward the p-value calculation of the three tests. In practice, permutation is commonly used to obtain accurate p-values, but it is computationally very intensive, especially when we need to conduct a large amount of hypothesis testing. In this paper, we propose a Gaussian approximation method based on a Monte Carlo scheme, which is computationally more efficient than permutation while still achieving similar accuracy. We derive nonasymptotic approximation error bounds that could vanish in the limit even if the number of covariates is much larger than the sample size. Through real-genotype-based simulations and data analysis of a genome-wide association study of Crohn’s disease, we compare the accuracy and computation cost of our proposed method, of permutation, and of the method based on asymptotic distribution. Supplementary materials for this article are available online.

笔记与分组