bioRxivBioinformaticsPreprint
PGCN: Disease gene prioritization by disease and gene embedding through graph convolutional neural networks
Yu LiiD, Hiroyuki KuwaharaiD, Peng YangiD, Le SongiD, Xin GaoiD
Abstract
MotivationProper prioritization of candidate genes is essential to the genome-based diagnostics of a range of genetic diseases. However, it is a highly challenging task involving limited and noisy knowledge of genes, diseases and their associations. While a number of computational methods have been developed for the disease gene prioritization task, their performance is largely limited by manually crafted features, network topology, or pre-defined rules of data fusion. ResultsHere, we propose a novel graph convolutional network-based disease gene prioritization method, PGCN, through the systematic embedding of the heterogeneous network made by genes and diseases, as well as their individual features. The embedding learning model and the association prediction model are trained together in an end-to-end manner. We compared PGCN with five state-of-the-art methods on the Online Mendelian Inheritance in Man (OMIM) dataset for tasks to recover missing associations and discover associations between novel genes and diseases. Results show significant improvements of PGCN over the existing methods. We further demonstrate that our embedding has biological meaning and can capture functional groups of genes. AvailabilityThe main program and the data are available at https://github.com/lykaust15/Disease_gene_prioritization_GCN.
Abstract summary
Claude Opus 5.5 · xhigh effort · 2 Nov 2026 · from the abstract
PGCN jointly trains graph convolutional network embeddings and association prediction on a heterogeneous gene-disease network to prioritize candidate disease genes and recover missing associations in OMIM.
Existing computational methods for prioritizing candidate disease genes from noisy, incomplete association data are constrained by manually engineered features, fixed network topology, or predefined data fusion rules. PGCN overcomes these constraints by jointly learning node embeddings and association predictions end-to-end on a heterogeneous network of genes, diseases, and their individual features.
Key results
ShownPGCN outperforms existing disease gene prioritization methods on both recovering missing associations and predicting associations involving uncharacterized genes and diseases.
Evaluated against 5 competing methods on the Online Mendelian Inheritance in Man (OMIM) dataset (specific evaluation metrics and numerical scores are not stated in the abstract). · Abstract
ShownLearned PGCN node embeddings organize genes into biologically meaningful functional groups.
Qualitative claim of capturing functional gene groups from the heterogeneous network embedding, with no quantitative clustering or enrichment numbers reported in the abstract. · Abstract
Methods, data and reproducibility
PGCN constructs a heterogeneous network combining genes, diseases, and their individual node features, and uses a graph convolutional network to learn low-dimensional embeddings. The embedding module and the gene-disease association predictor are trained jointly end-to-end and evaluated on the Online Mendelian Inheritance in Man (OMIM) dataset against 5 baseline methods.
- Online Mendelian Inheritance in Man (OMIM) gene-disease association dataset · human (inferred from Online Mendelian Inheritance in Man, OMIM)
- Methods & tools
- PGCN, Online Mendelian Inheritance in Man (OMIM)
- Data & accessions
- https://github.com/lykaust15/Disease_gene_prioritization_GCN
- Reproducibility gaps
- Software environment, dependencies, and compute resource requirements are not reported in the abstract.
Limitations (2)
- The abstract does not report quantitative performance numbers, dataset sizes, or the identities of the 5 baseline methods compared on OMIM. · noted in this summary
- Benchmarking described in the abstract is limited to a single database (OMIM). · noted in this summary
Read this if you work on computational disease gene prioritization or gene-disease association prediction and want an end-to-end graph convolutional network approach.
- Citations
- 57
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