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arXiv 2602.22975stat.ME

permApprox: 一种用于准确置换p值近似的通用框架

permApprox: a general framework for accurate permutation p-value approximation

Stefanie Peschel, Anne-Laure Boulesteix, Erika von Mutius, Christian L. Müller

AI总结:

permApprox通过广义极值分布建模和约束支持,解决置换检验中零p值问题,提供准确且无零的p值近似,适用于高维数据和计算密集型场景。

摘要:

置换检验在假设检验中常用于当对检验统计量的分布假设不成立或未知时。仅使用少量置换时,经验p值会落在较粗的网格上,甚至当观察到的检验统计量超过所有置换值时可能为零。此类零p值在统计上无效,并阻碍多重检验校正。参数尾部建模使用广义极值分布(GPD)已被提出以解决此问题,但现有实现当估计的形状参数为负且拟合分布有有限上界时仍可能产生零p值。我们介绍了一种用于置换检验中准确且无零p值近似的 方法,嵌入在permApprox工作流和R包中。基于GPD尾部建模,该方法在参数估计期间施加支持约束以确保在观察到的统计量之外的正确外推,从而严格避免零p值。工作流进一步整合了稳健的参数估计、数据驱动的阈值选择以及对混合p值的处理,这些p值在主体部分是离散的,在极端尾部是连续的。使用两样本t检验和Wilcoxon秩和检验的广泛模拟显示,permApprox在广泛的样本和效应大小范围内产生准确、稳健且无零的p值近似。应用于单细胞RNA测序和微生物组数据的实验证明了其实际效用:permApprox即使在少量置换时也能产生平滑且可解释的p值分布。通过解决零p值问题的同时保持准确性和计算效率,permApprox在高维和计算密集型设置中实现了可靠的置换推理。

英文摘要:

Permutation procedures are common practice in hypothesis testing when distributional assumptions about the test statistic are not met or unknown. With only few permutations, empirical p-values lie on a coarse grid and may even be zero when the observed test statistic exceeds all permuted values. Such zero p-values are statistically invalid and hinder multiple testing correction. Parametric tail modeling with the Generalized Pareto Distribution (GPD) has been proposed to address this issue, but existing implementations can again yield zero p-values when the estimated shape parameter is negative and the fitted distribution has a finite upper bound. We introduce a method for accurate and zero-free p-value approximation in permutation testing, embedded in the permApprox workflow and R package. Building on GPD tail modeling, the method enforces a support constraint during parameter estimation to ensure valid extrapolation beyond the observed statistic, thereby strictly avoiding zero p-values. The workflow further integrates robust parameter estimation, data-driven threshold selection, and principled handling of hybrid p-values that are discrete in the bulk and continuous in the extreme tail. Extensive simulations using two-sample t-tests and Wilcoxon rank-sum tests show that permApprox produces accurate, robust, and zero-free p-value approximations across a wide range of sample and effect sizes. Applications to single-cell RNA-seq and microbiome data demonstrate its practical utility: permApprox yields smooth and interpretable p-value distributions even with few permutations. By resolving the zero-p-value problem while preserving accuracy and computational efficiency, permApprox enables reliable permutation-based inference in high-dimensional and computationally intensive settings.

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