Evidence map›Paper›PMID 39154194›Full record

ArticleBriefings in bioinformatics2024

Heterogeneous biomedical entity representation learning for gene-disease association prediction.

Zhaohan Meng, Siwei Liu, Shangsong Liang, Bhautesh Jani, Zaiqiao Meng

Abstract read
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Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zhaohan MengSchool of Computing Science, University of Glasgow, 18 Lilybank Gardens, Glasgow G12 8RZ, UK.
Siwei LiuSchool of Natural and Computing Science, University of Aberdeen King's College, Aberdeen, AB24 3FX, UK.ORCID 0000-0002-7326-2883
Shangsong LiangMachine Learning Department, Mohamed bin Zayed University of Artificial Intelligence, Building 1B, Masdar City, Abu Dhabi 000000, UAE.
Bhautesh JaniSchool of Computing Science, University of Glasgow, 18 Lilybank Gardens, Glasgow G12 8RZ, UK.
Zaiqiao MengSchool of Computing Science, University of Glasgow, 18 Lilybank Gardens, Glasgow G12 8RZ, UK.ORCID 0000-0001-5374-0318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the genetic basis of disease is a fundamental aspect of medical research, as genes are the classic units of heredity and play a crucial role in biological function. Identifying associations between genes and diseases is critical for diagnosis, prevention, prognosis, and drug development. Genes that encode proteins with similar sequences are often implicated in related diseases, as proteins causing identical or similar diseases tend to show limited variation in their sequences. Predicting gene-disease association (GDA) requires time-consuming and expensive experiments on a large number of potential candidate genes. Although methods have been proposed to predict associations between genes and diseases using traditional machine learning algorithms and graph neural networks, these approaches struggle to capture the deep semantic information within the genes and diseases and are dependent on training data. To alleviate this issue, we propose a novel GDA prediction model named FusionGDA, which utilizes a pre-training phase with a fusion module to enrich the gene and disease semantic representations encoded by pre-trained language models. Multi-modal representations are generated by the fusion module, which includes rich semantic information about two heterogeneous biomedical entities: protein sequences and disease descriptions. Subsequently, the pooling aggregation strategy is adopted to compress the dimensions of the multi-modal representation. In addition, FusionGDA employs a pre-training phase leveraging a contrastive learning loss to extract potential gene and disease features by training on a large public GDA dataset. To rigorously evaluate the effectiveness of the FusionGDA model, we conduct comprehensive experiments on five datasets and compare our proposed model with five competitive baseline models on the DisGeNet-Eval dataset. Notably, our case study further demonstrates the ability of FusionGDA to discover hidden associations effectively. The complete code and datasets of our experiments are available at https://github.com/ZhaohanM/FusionGDA.

Indexed as

Machine LearningAlgorithmsComputational BiologyGenetic Association StudiesGenetic Predisposition to DiseaseHumansNeural Networks, ComputerSemanticscontrastive learningdiseasefusion modulegenepre-trained language modelpre-training

Identifiers

PMID39154194
PMCPMC11330343

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.