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GNN4DM: a graph neural network-based method to identify overlapping functional disease modules.

Authors :
Gézsi A
Antal P
Source :
Bioinformatics (Oxford, England) [Bioinformatics] 2024 Oct 01; Vol. 40 (10).
Publication Year :
2024

Abstract

Motivation: Identifying disease modules within molecular interaction networks is an essential exploratory step in computational biology, offering insights into disease mechanisms and potential therapeutic targets. Traditional methods often struggle with the inherent complexity and overlapping nature of biological networks, and they are limited in effectively leveraging the vast amount of available genomic data and biological knowledge. This limitation underscores the need for more effective, automated approaches to integrate these rich data sources.<br />Results: In this work, we propose GNN4DM, a novel graph neural network-based structured model that automates the discovery of overlapping functional disease modules. GNN4DM effectively integrates network topology with genomic data to learn the representations of the genes corresponding to functional modules and align these with known biological pathways for enhanced interpretability. Following the DREAM benchmark evaluation setting and extending with three independent data sources (GWAS Atlas, FinnGen, and DisGeNET), we show that GNN4DM performs better than several state-of-the-art methods in detecting biologically meaningful modules. Moreover, we demonstrate the method's applicability by discovering two novel multimorbidity modules significantly enriched across a diverse range of seemingly unrelated diseases.<br />Availability and Implementation: Source code, all training data, and all identified disease modules are freely available for download at https://github.com/gezsi/gnn4dm. GNN4DM was implemented in Python.<br /> (© The Author(s) 2024. Published by Oxford University Press.)

Details

Language :
English
ISSN :
1367-4811
Volume :
40
Issue :
10
Database :
MEDLINE
Journal :
Bioinformatics (Oxford, England)
Publication Type :
Academic Journal
Accession number :
39321259
Full Text :
https://doi.org/10.1093/bioinformatics/btae573