Evidence map›Paper›PMID 41307874›Full record

ArticleInterdisciplinary sciences, computational life sciences2026

DSGCNLDA: A Multi-view Learning Model with DualScope Attention for lncRNA-Disease Association Prediction.

Dengju Yao, Zhanhe Li, Xiaojuan Zhan, Bo Zhang, Xiangkui Li

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Article in Interdisciplinary sciences, computational life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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5 · Who and what money

Authors and funding

5 authors.

Dengju YaoSchool of Computer Science and Technology, Harbin University of Science and Technology, Harbin, 150080, China. ydkvictory@hrbust.edu.cn.ORCID http://orcid.org/0000-0002-4974-3054
Zhanhe LiSchool of Computer Science and Technology, Harbin University of Science and Technology, Harbin, 150080, China.
Xiaojuan ZhanCollege of Computer Science and Technology, Heilongjiang Institute of Technology, Harbin, 150050, China.
Bo ZhangSchool of Modern Industry and Health Management, Jinzhou Medical University, Jinzhou, 121001, China.
Xiangkui LiSchool of Computer Science and Technology, Harbin University of Science and Technology, Harbin, 150080, China.

Funding

National Natural Science Foundation of China Grant No. 62172128
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) play key regulatory roles in biological activities, making it crucial to accurately predict lncRNA-disease relationships for understanding disease pathophysiology and developing effective prevention and treatment strategies. Nevertheless, existing computational prediction methods are often limited by data sparsity and incompleteness, as well as the inadequate representation of node information. To mitigate these issues, a novel prediction model, termed DSGCNLDA, is proposed to enhance predictive performance. The proposed model integrates biological similarity features from multiple perspectives into a comprehensive similarity matrix using multi-view fusion learning. Utilizing this similarity matrix in conjunction with the adjacency matrix, a heterogeneous network of lncRNA-disease associations is constructed. Subsequently, feature extraction is conducted on the randomly masked heterogeneous network. During this process, a graph convolutional network (GCN) is employed as the encoder, and our proposed DualScope attention mechanism is introduced to more effectively capture complex topological relationships between nodes, thereby obtaining a comprehensive representation of the nodes. Finally, association prediction is made via a multi-layer perceptron (MLP). Experimental results on multiple public datasets show that DSGCNLDA performs strongly in lncRNA-disease association prediction. Ablation studies confirm its novelty, while case studies and generalization evaluations demonstrate its effectiveness in biomedical prediction tasks.

Indexed as

Computational BiologyGenetic Predisposition to DiseaseRNA, Long NoncodingAlgorithmsGraph Neural NetworksHumansMultilayer PerceptronsPrediction AlgorithmsPredictive Learning ModelsRNA, Long NoncodingDeep learningGraph attention mechanismlncRNA–disease associationMulti-view learning

Identifiers

PMID41307874

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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 Socratic graph.