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Biometrika· 2026Q1

Saddlepoint approximations for plug-in resampling

Ziang Niu, Zhihan Huang, Jyotishka Ray Choudhury, Eugene Katsevich

Short summary

A new method uses saddlepoint approximations to speed up plug-in resampling statistical tests by up to 250-fold, offering analytical guarantees for accuracy in sparse, large-scale settings.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Introduces saddlepoint approximation as a faster alternative to plug-in resampling for statistical tests.
  • Establishes a finite-sample relative-error bound for the Lugannani–Rice approximation under tractable conditions.
  • Applies the method to statistical genetics and conditional independence testing, providing theoretical guarantees.
  • Achieves up to a 250-fold acceleration in computational speed in simulations and single-cell CRISPR data analysis.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Resampling-based procedures can improve on normal approximations in sparse, large-scale testing problems, but their computational cost can be prohibitive. We recognize that several existing procedures belong to a faster plug-in resampling subclass, fixing fitted nuisance parameters during resampling. When the resampled statistic is a sum of conditionally independent terms, the saddlepoint approximation for the resampling p -value offers further acceleration, replacing resampling with an analytical tail approximation. However, standard Edgeworth-based approximation-error bounds impose regularity conditions that are hard to verify for plug-in resampling laws. We use an alternative approach to establish a finite-sample relative-error bound for the Lugannani–Rice approximation under more tractable conditions, which we apply in two contexts. In statistical genetics, we identify response resampling procedures as the targets of existing saddlepoint approximations and establish guarantees in a representative setting. In conditional independence testing, we introduce a saddlepoint approximation for the distilled conditional randomization test, which has been applied successfully in biology. Our rates quantify the effects of sparsity and signal strength, with matching lower bounds in special cases. We additionally establish asymptotic Type-I error control of the corresponding plug-in resampling procedures under growing sparsity. In simulations and single-cell CRISPR data analysis, our new test closely approximates distilled conditional randomization test p -values and preserves its statistical performance while accelerating computation by up to 250-fold.

The authors' abstract, as published at the source. Biometrika, 2026 · DOI ↗

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Field: Statistics and Probability

Statistics and ProbabilityMathematics