Evidence map›Paper›PMID 40495794›Full record

ArticleBriefings in bioinformatics2025

HGCMLDA: predicting lncRNA-disease associations using hypergraph contrastive learning and multi-scale attentional feature fusion.

Zequn Zhang, Huijun Li, Yuxi Chen, Xiaoli Li, Dongqing Wei, Hongyan Wu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Zequn ZhangShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Huijun LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Yuxi ChenShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Xiaoli LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Dongqing WeiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.
Hongyan WuShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.

Funding

National Natural Science Foundation of China 62273322Natural Science Foundation of Guangdong Province 2024A1515012269Shenzhen Medical Research Fund D2401005
6 · The paper itself

Abstract

Research has consistently indicated that long non-coding RNAs (lncRNAs) significantly influence the development of numerous diseases. Predicting lncRNA-disease associations (LDAs) will contribute to the prevention and treatment of diseases. However, most existing computational models suffer from several challenges: (i) difficulty in capturing complex higher-order relationships among nodes; (ii) limited number of known associations and neglect of consistency of representations across views; (iii) inadequate fusion of multi-view data. In this research, we introduce an innovative end-to-end method named HGCMLDA for LDA prediction. Firstly, HGCMLDA constructs hypergraphs of lncRNAs and diseases based on integrated similarity matrices utilizing Gaussian mixture model and k-nearest neighbor methods and utilizes hypergraph convolutional network to extract high-order representations of lncRNAs and diseases, followed by contrastive learning to capture information interaction between different views that can alleviate the dependence on limited known associations and enhance the node representations in an unsupervised way. Then, HGCMLDA utilizes multi-scale attentional feature fusion, which considers importance weights of different views and aggregates both global and local context to achieve achieve effective and adequate feature fusion. Subsequently, disease features and lncRNA features are also extracted by using variational autoencoder on the association matrix, so that prior knowledge is effectively incorporated for prediction. Finally, the features of these two parts are concatenated, and matrix completion is performed to predict LDA scores. The results of the comparison experiments indicate that HGCMLDA outperforms five state-of-the-art models for LDA prediction. Case studies for specific diseases demonstrate that HGCMLDA can identify novel associations with high accuracy.

Indexed as

Computational BiologyGenetic Predisposition to DiseaseRNA, Long NoncodingAlgorithmsHumansRNA, Long Noncodingcontrastive learninghypergraph convolutional networklncRNA-disease association predictionmulti-scale attentional feature fusion

Identifiers

PMID40495794
PMCPMC12152417

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

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.