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Main Authors: Oh, Sangkon, McLachlan, Geoffrey J.
Format: Preprint
Published: 2026
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Online Access:https://arxiv.org/abs/2603.01381
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author Oh, Sangkon
McLachlan, Geoffrey J.
author_facet Oh, Sangkon
McLachlan, Geoffrey J.
contents Two-component mixture models are particularly useful for identifying differentially expressed genes, but their performance can deteriorate markedly when the alternative distribution departs from parametric assumptions or symmetry. We propose a semiparametric mixture model in which the null component is standard normal and the alternative follows a skew-normal scale mixture with an unspecified scale mixing distribution. This formulation accommodates skewness and heavy tails, providing a flexible and computationally tractable tool for differential gene-expression analysis without restrictive distributional assumptions. We establish identifiability and consistency of the model and develop an efficient estimation algorithm that incorporates nonparametric maximum likelihood estimation of the scale distribution. Numerical studies show notable improvements over existing parametric and nonparametric approaches for modeling the alternative distribution, and applications to colon cancer and leukemia datasets demonstrate reduced false discovery and false negative rates.
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id arxiv_https___arxiv_org_abs_2603_01381
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Differential gene expression analysis via two-component mixture models with a semiparametric skew-normal scale mixture alternative
Oh, Sangkon
McLachlan, Geoffrey J.
Methodology
Two-component mixture models are particularly useful for identifying differentially expressed genes, but their performance can deteriorate markedly when the alternative distribution departs from parametric assumptions or symmetry. We propose a semiparametric mixture model in which the null component is standard normal and the alternative follows a skew-normal scale mixture with an unspecified scale mixing distribution. This formulation accommodates skewness and heavy tails, providing a flexible and computationally tractable tool for differential gene-expression analysis without restrictive distributional assumptions. We establish identifiability and consistency of the model and develop an efficient estimation algorithm that incorporates nonparametric maximum likelihood estimation of the scale distribution. Numerical studies show notable improvements over existing parametric and nonparametric approaches for modeling the alternative distribution, and applications to colon cancer and leukemia datasets demonstrate reduced false discovery and false negative rates.
title Differential gene expression analysis via two-component mixture models with a semiparametric skew-normal scale mixture alternative
topic Methodology
url https://arxiv.org/abs/2603.01381