{"title":"HGATLink: single-cell gene regulatory network inference via the fusion of heterogeneous graph attention networks and transformer.","authors":"Yao Sun, Jing Gao","doi":"10.1186/s12859-025-06071-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Gene regulatory networks (GRNs) involve complex regulatory relationships between genes and play important roles in the study of various biological systems and diseases. The introduction of single-cell sequencing (scRNA-seq) technology has allowed gene regulation studies to be carried out on specific cell types, providing the opportunity to accurately infer gene regulatory networks. However, the sparsity and noise problems of single-cell sequencing data pose challenges for gene regulatory network inference, and although many gene regulatory network inference methods have been proposed, they often fail to eliminate transitive interactions or do not address multilevel relationships and nonlinear features in the graph data well.</p><p><strong>Results: </strong>On the basis of the above limitations, we propose a gene regulatory network inference framework named HGATLink. HGATLink combines the heterogeneous graph attention network and simplified transformer to capture complex interactions effectively between genes in low-dimensional space via matrix decomposition techniques, which not only enhances the ability to model complex heterogeneous graph structures and alleviate transitive interactions, but also effectively captures the long-range dependencies between genes to ensure more accurate prediction.</p><p><strong>Conclusions: </strong>Compared with 10 state-of-the-art GRN inference methods on 14 scRNA-seq datasets under two metrics, AUROC and AUPRC, HGATLink shows good stability and accuracy in gene regulatory network inference tasks.</p>","PeriodicalId":8958,"journal":{"name":"BMC Bioinformatics","volume":"26 1","pages":"49"},"PeriodicalIF":2.9000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12859-025-06071-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Gene regulatory networks (GRNs) involve complex regulatory relationships between genes and play important roles in the study of various biological systems and diseases. The introduction of single-cell sequencing (scRNA-seq) technology has allowed gene regulation studies to be carried out on specific cell types, providing the opportunity to accurately infer gene regulatory networks. However, the sparsity and noise problems of single-cell sequencing data pose challenges for gene regulatory network inference, and although many gene regulatory network inference methods have been proposed, they often fail to eliminate transitive interactions or do not address multilevel relationships and nonlinear features in the graph data well.
Results: On the basis of the above limitations, we propose a gene regulatory network inference framework named HGATLink. HGATLink combines the heterogeneous graph attention network and simplified transformer to capture complex interactions effectively between genes in low-dimensional space via matrix decomposition techniques, which not only enhances the ability to model complex heterogeneous graph structures and alleviate transitive interactions, but also effectively captures the long-range dependencies between genes to ensure more accurate prediction.
Conclusions: Compared with 10 state-of-the-art GRN inference methods on 14 scRNA-seq datasets under two metrics, AUROC and AUPRC, HGATLink shows good stability and accuracy in gene regulatory network inference tasks.
期刊介绍:
BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology.
BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.