Identifying High-Dimensional Genomic Factors Modulating Biological Networks Across Multi-Omics Data

Biological traits such as genes, metabolites, and microbial taxa interact within complex networks, yet how genomic factors shape these interactions remains poorly understood. Here, we introduce GFBioNet, a computationally efficient method for identifying factors that modulate direct associations between biological traits within network models. Our two-stage strategy first estimates a baseline network using Gaussian graphical models and then tests whether genomic factors modulate specific network edges (trait-trait relationships), enabling scalable analysis of high-dimensional multi-omics data while explicitly controlling the false discovery rate (FDR). Simulations demonstrate reliable FDR control and high statistical power across a broad range of settings. Applied to multiple datasets, GFBioNet reveals host genetic variants influencing oral microbiome relationships, gut microbial taxa modulating metabolite networks in colorectal cancer, and somatic mutations and copy-number alterations reshaping gene expression networks in lung adenocarcinoma. By expanding network analysis to evaluate modifiers of trait-trait relationships, GFBioNet offers a versatile tool for uncovering the genomic architecture of biological networks across multi-omics studies.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-22
DOI
https://doi.org/10.64898/2025.12.18.695273
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
0.00

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article

Identifying High-Dimensional Genomic Factors Modulating Biological Networks Across Multi-Omics Data

Christian C. Abnet, Samuel Anyaso‐Samuel, Emily Vogtmann, Fei Qin et al.
bioRxiv (Cold Spring Harbor Laboratory)
Bioinformatics and Genomic Networks
article

Identifying High-Dimensional Genomic Factors Modulating Biological Networks Across Multi-Omics Data

Christian C. Abnet, Samuel Anyaso‐Samuel, Emily Vogtmann, Fei Qin, Xing Hua, Paul Albert, Mohammad Jellur Rahman, Xiaohong Yang, Kai Yu, Kevin Brown, Giovanny Herrera-Ossa, Maria Teresa Landi, Tongwu Zhang, Jianxin Shi, Steven Moore, Shilan Li, Bin Zhu, Wei Zhao, Xiaoyu Wang
article en

Abstract

Biological traits such as genes, metabolites, and microbial taxa interact within complex networks, yet how genomic factors shape these interactions remains poorly understood. Here, we introduce GFBioNet, a computationally efficient method for identifying factors that modulate direct associations between biological traits within network models. Our two-stage strategy first estimates a baseline network using Gaussian graphical models and then tests whether genomic factors modulate specific network edges (trait-trait relationships), enabling scalable analysis of high-dimensional multi-omics data while explicitly controlling the false discovery rate (FDR). Simulations demonstrate reliable FDR control and high statistical power across a broad range of settings. Applied to multiple datasets, GFBioNet reveals host genetic variants influencing oral microbiome relationships, gut microbial taxa modulating metabolite networks in colorectal cancer, and somatic mutations and copy-number alterations reshaping gene expression networks in lung adenocarcinoma. By expanding network analysis to evaluate modifiers of trait-trait relationships, GFBioNet offers a versatile tool for uncovering the genomic architecture of biological networks across multi-omics studies.

bioRxiv (Cold Spring Harbor Laboratory)
Johns Hopkins University (US), National Cancer Institute (US), Department of Health and Human Services (US)
National Institutes of Health
Openalex Percentile: Top 37%
Bioinformatics and Genomic Networks
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