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A Deep Learning Framework for Predicting Disease-gene Associations with Functional Modules and Graph Augmentation

Overview
Publisher Biomed Central
Specialty Biology
Date 2024 Jun 14
PMID 38877401
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Abstract

Background: The exploration of gene-disease associations is crucial for understanding the mechanisms underlying disease onset and progression, with significant implications for prevention and treatment strategies. Advances in high-throughput biotechnology have generated a wealth of data linking diseases to specific genes. While graph representation learning has recently introduced groundbreaking approaches for predicting novel associations, existing studies always overlooked the cumulative impact of functional modules such as protein complexes and the incompletion of some important data such as protein interactions, which limits the detection performance.

Results: Addressing these limitations, here we introduce a deep learning framework called ModulePred for predicting disease-gene associations. ModulePred performs graph augmentation on the protein interaction network using L3 link prediction algorithms. It builds a heterogeneous module network by integrating disease-gene associations, protein complexes and augmented protein interactions, and develops a novel graph embedding for the heterogeneous module network. Subsequently, a graph neural network is constructed to learn node representations by collectively aggregating information from topological structure, and gene prioritization is carried out by the disease and gene embeddings obtained from the graph neural network. Experimental results underscore the superiority of ModulePred, showcasing the effectiveness of incorporating functional modules and graph augmentation in predicting disease-gene associations. This research introduces innovative ideas and directions, enhancing the understanding and prediction of gene-disease relationships.

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References
1.
Ghiassian S, Menche J, Barabasi A . A DIseAse MOdule Detection (DIAMOnD) algorithm derived from a systematic analysis of connectivity patterns of disease proteins in the human interactome. PLoS Comput Biol. 2015; 11(4):e1004120. PMC: 4390154. DOI: 10.1371/journal.pcbi.1004120. View

2.
Stoupa A, Adam F, Kariyawasam D, Strassel C, Gawade S, Szinnai G . TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology. EMBO Mol Med. 2018; 10(12). PMC: 6284387. DOI: 10.15252/emmm.201809569. View

3.
Yoon S, Nguyen H, Yoo Y, Kim J, Baik B, Kim S . Efficient pathway enrichment and network analysis of GWAS summary data using GSA-SNP2. Nucleic Acids Res. 2018; 46(10):e60. PMC: 6007455. DOI: 10.1093/nar/gky175. View

4.
Jowkar G, Mansoori E . Perceptron ensemble of graph-based positive-unlabeled learning for disease gene identification. Comput Biol Chem. 2016; 64:263-270. DOI: 10.1016/j.compbiolchem.2016.07.004. View

5.
Lotfi Shahreza M, Ghadiri N, Mousavi S, Varshosaz J, Green J . A review of network-based approaches to drug repositioning. Brief Bioinform. 2017; 19(5):878-892. DOI: 10.1093/bib/bbx017. View