A statistical physics approach to integrating multi-omics data for disease-module detection

Genes associated with the same disease frequently engage in mutual biological interactions, e.g., perturbation within a specific neighborhood in the molecular interactome, often referred to as the disease module. This has propelled the advancement of network-based approaches toward elucidating the molecular bases of human diseases. Although many computational methods have been developed to integrate the molecular interactome and omics profiles to extract such context-dependent disease modules, approaches that leverage multi-omics for disease-module detection are still lacking. Here, we developed a statistical physics approach based on the random-field O(n) model (RFOnM) to fill this gap. We applied the RFOnM approach to integrate gene-expression data and genome-wide association studies or mRNA data and DNA methylation for several complex diseases with the human interactome. We found that the RFOnM approach outperforms existing single omics methods in most of the complex diseases considered in this study.

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Publication Details

Journal
Cell Reports Methods
Published
2025-09-23
DOI
https://doi.org/10.1016/j.crmeth.2025.101183
Primary Topic
Bioinformatics and Genomic Networks
Type
article
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article

A statistical physics approach to integrating multi-omics data for disease-module detection

Xu‐Wen Wang, Yang‐Yu Liu, Min Hyung Ryu, Craig P. Hersh et al.
Cell Reports Methods
Bioinformatics and Genomic Networks
article

A statistical physics approach to integrating multi-omics data for disease-module detection

Xu‐Wen Wang, Yang‐Yu Liu, Min Hyung Ryu, Craig P. Hersh, Edwin K. Silverman, Michael H. Cho, Peter J. Castaldi
article en

Abstract

Genes associated with the same disease frequently engage in mutual biological interactions, e.g., perturbation within a specific neighborhood in the molecular interactome, often referred to as the disease module. This has propelled the advancement of network-based approaches toward elucidating the molecular bases of human diseases. Although many computational methods have been developed to integrate the molecular interactome and omics profiles to extract such context-dependent disease modules, approaches that leverage multi-omics for disease-module detection are still lacking. Here, we developed a statistical physics approach based on the random-field O(n) model (RFOnM) to fill this gap. We applied the RFOnM approach to integrate gene-expression data and genome-wide association studies or mRNA data and DNA methylation for several complex diseases with the human interactome. We found that the RFOnM approach outperforms existing single omics methods in most of the complex diseases considered in this study.

Cell Reports MethodsVol. 5(10)
Brigham and Women's Hospital (US), Harvard University (US), University of British Columbia (CA)
Openalex Percentile: Top 77%
Bioinformatics and Genomic Networks
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