Evidence map›Paper›PMID 40757912›Full record

ArticleBioinformatics (Oxford, England)2025

Double optimal transport for differential gene regulatory network inference with unpaired samples.

Mengyu Li, Bencong Zhu, Cheng Meng, Xiaodan Fan

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Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mengyu LiInstitute of Statistics and Big Data, Renmin University of China, Beijing 100872, China.ORCID 0000-0002-5286-7525
Bencong ZhuDepartment of Statistics, The Chinese University of Hong Kong, Hong Kong 999077, China.
Cheng MengCenter for Applied Statistics, Institute of Statistics and Big Data, Renmin University of China, Beijing 100872, China.
Xiaodan FanDepartment of Statistics, The Chinese University of Hong Kong, Hong Kong 999077, China.ORCID 0000-0002-2744-9030

Funding

Beijing Municipal Natural Science Foundation 1232019Renmin University of China Research Fund Program for Young ScholarsResearch Grants Council of Hong Kong SAR C7015-23G
6 · The paper itself

Abstract

motivationInferring differential gene regulatory networks (GRNs) between different conditions from gene expression profiles remains a significant challenge. Current GRN inference approaches are limited by either scalability in large networks or accuracy in high-dimensional scenarios. Furthermore, most existing methods require paired samples for comparative GRN analyses.

resultsTo overcome these challenges, we model gene regulation as a distribution transportation problem and propose an efficient and effective method, called double optimal transport (OT), for reconstructing differential GRNs from the perspective of optimal transport theory, applicable to unpaired samples. Double OT is a novel two-level OT framework. It first aligns unpaired samples by solving a partial OT problem at the sample level, and then infers GRNs from the aligned samples by solving a robust OT problem at the gene level. Comprehensive simulation studies demonstrate the superior efficiency and efficacy of double OT in different scales of networks compared to state-of-the-art methods. We also apply the proposed method to a gastric cancer dataset, identifying the proto-oncogene MET as a central node in the gastric cancer GRN. Its crucial role in early oncogenesis and potential as a therapeutic target further validate our approach and enhance our understanding of the regulatory mechanisms of gastric cancer. AVAILABILITY AND IMPLEMENTATION: A Python library that implements the proposed method is available at https://github.com/Mengyu8042/ot-grn.

Indexed as

Computational BiologyGene Regulatory NetworksAlgorithmsGene Expression ProfilingHumansProto-Oncogene MasStomach NeoplasmsMAS1 protein, humanProto-Oncogene Mas

Identifiers

PMID40757912
PMCPMC12342166

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