MetaGeno: a chromosome-wise multi-task genomic framework for ischaemic stroke risk prediction.
- Publisher:
- Oxford University Press (OUP)
- Publication Type:
- Journal Article
- Citation:
- Brief Bioinform, 2025, 26, (4), pp. bbaf348
- Issue Date:
- 2025-07-02
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, Y | |
dc.contributor.author |
Guo, K |
|
dc.contributor.author | Zhang, Y | |
dc.contributor.author | Fang, Z | |
dc.contributor.author | Lin, H | |
dc.contributor.author | Grosser, M | |
dc.contributor.author | Venter, D | |
dc.contributor.author | Lu, W | |
dc.contributor.author |
Wu, M |
|
dc.contributor.author | Cordato, D | |
dc.contributor.author |
Zhang, G |
|
dc.contributor.author | Lu, J | |
dc.date.accessioned | 2025-07-29T02:30:52Z | |
dc.date.available | 2025-06-16 | |
dc.date.available | 2025-07-29T02:30:52Z | |
dc.date.issued | 2025-07-02 | |
dc.identifier.citation | Brief Bioinform, 2025, 26, (4), pp. bbaf348 | |
dc.identifier.issn | 1467-5463 | |
dc.identifier.issn | 1477-4054 | |
dc.identifier.uri | http://hdl.handle.net/10453/188868 | |
dc.description.abstract | Current genome-wide association studies provide valuable insights into the genetic basis of ischaemic stroke (IS) risk. However, polygenic risk scores, the most widely used method for genetic risk prediction, have notable limitations due to their linear nature and inability to capture complex, nonlinear interactions among genetic variants. While deep neural networks offer advantages in modeling these complex relationships, the multifactorial nature of IS and the influence of modifiable risk factors present additional challenges for genetic risk prediction. To address these challenges, we propose a Chromosome-wise Multi-task Genomic (MetaGeno) framework that utilizes genetic data from IS and five related diseases. The framework includes a chromosome-based embedding layer to model local and global interactions among adjacent variants, enabling a biologically informed approach. Incorporating multi-disease learning further enhances predictive accuracy by leveraging shared genetic information. Among various sequential models tested, the Transformer demonstrated superior performance, and outperformed other machine learning models and PRS baselines, achieving an AUROC of 0.809 on the UK Biobank dataset. Risk stratification identified a two-fold increased stroke risk (HR, 2.14; 95% CI: 1.81-2.46) in the top 1% risk group, with a nearly five-fold increase in those with modifiable risk factors such as atrial fibrillation and hypertension. Finally, the model was validated on the diverse All of Us dataset (AUROC = 0.764), highlighting ancestry and population differences while demonstrating effective generalization. This study introduces a predictive framework that identifies high-risk individuals and informs targeted prevention strategies, offering potential as a clinical decision-support tool. | |
dc.language | eng | |
dc.publisher | Oxford University Press (OUP) | |
dc.relation | http://purl.org/au-research/grants/arc/LP210100414 | |
dc.relation.ispartof | Brief Bioinform | |
dc.relation.isbasedon | 10.1093/bib/bbaf348 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0601 Biochemistry and Cell Biology, 0802 Computation Theory and Mathematics, 0899 Other Information and Computing Sciences | |
dc.subject.classification | Bioinformatics | |
dc.subject.classification | 3101 Biochemistry and cell biology | |
dc.subject.classification | 3102 Bioinformatics and computational biology | |
dc.subject.classification | 3105 Genetics | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Ischemic Stroke | |
dc.subject.mesh | Risk Factors | |
dc.subject.mesh | Genomics | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Genome-Wide Association Study | |
dc.subject.mesh | Machine Learning | |
dc.subject.mesh | Risk Assessment | |
dc.subject.mesh | Stroke | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Ischemic Stroke | |
dc.subject.mesh | Risk Factors | |
dc.subject.mesh | Genomics | |
dc.subject.mesh | Genetic Predisposition to Disease | |
dc.subject.mesh | Genome-Wide Association Study | |
dc.subject.mesh | Machine Learning | |
dc.subject.mesh | Risk Assessment | |
dc.subject.mesh | Stroke | |
dc.subject.mesh | Female | |
dc.title | MetaGeno: a chromosome-wise multi-task genomic framework for ischaemic stroke risk prediction. | |
dc.type | Journal Article | |
utslib.citation.volume | 26 | |
utslib.location.activity | England | |
utslib.for | 0601 Biochemistry and Cell Biology | |
utslib.for | 0802 Computation Theory and Mathematics | |
utslib.for | 0899 Other Information and Computing Sciences | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Computer Science | |
pubs.organisational-group | University of Technology Sydney/UTS Groups | |
pubs.organisational-group | University of Technology Sydney/UTS Groups/Australian Artificial Intelligence Institute (AAII) | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2025-07-29T02:30:51Z | |
pubs.issue | 4 | |
pubs.publication-status | Published | |
pubs.volume | 26 | |
utslib.citation.issue | 4 |
Abstract:
Current genome-wide association studies provide valuable insights into the genetic basis of ischaemic stroke (IS) risk. However, polygenic risk scores, the most widely used method for genetic risk prediction, have notable limitations due to their linear nature and inability to capture complex, nonlinear interactions among genetic variants. While deep neural networks offer advantages in modeling these complex relationships, the multifactorial nature of IS and the influence of modifiable risk factors present additional challenges for genetic risk prediction. To address these challenges, we propose a Chromosome-wise Multi-task Genomic (MetaGeno) framework that utilizes genetic data from IS and five related diseases. The framework includes a chromosome-based embedding layer to model local and global interactions among adjacent variants, enabling a biologically informed approach. Incorporating multi-disease learning further enhances predictive accuracy by leveraging shared genetic information. Among various sequential models tested, the Transformer demonstrated superior performance, and outperformed other machine learning models and PRS baselines, achieving an AUROC of 0.809 on the UK Biobank dataset. Risk stratification identified a two-fold increased stroke risk (HR, 2.14; 95% CI: 1.81-2.46) in the top 1% risk group, with a nearly five-fold increase in those with modifiable risk factors such as atrial fibrillation and hypertension. Finally, the model was validated on the diverse All of Us dataset (AUROC = 0.764), highlighting ancestry and population differences while demonstrating effective generalization. This study introduces a predictive framework that identifies high-risk individuals and informs targeted prevention strategies, offering potential as a clinical decision-support tool.
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