Evidence map›Paper›PMID 38652712›Full record

ArticlePLoS computational biology2024

HGCLAMIR: Hypergraph contrastive learning with attention mechanism and integrated multi-view representation for predicting miRNA-disease associations.

Dong Ouyang, Yong Liang, Jinfeng Wang, Le Li, Ning Ai, Junning Feng, Shanghui Lu, Shuilin Liao, Xiaoying Liu, Shengli Xie

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

10 authors.

Dong OuyangPeng Cheng Laboratory, Shenzhen, China.
Yong LiangPeng Cheng Laboratory, Shenzhen, China.ORCID 0000-0003-2403-1971
Jinfeng WangCollege of Mathematics and Informatics, South China Agricultural University, Guangzhou, China.
Le LiSchool of Computer Science and Engineering, Faculty of Innovation Engineering, Macau University of Science and Technology, Macau, China.
Ning AiSchool of Computer Science and Engineering, Faculty of Innovation Engineering, Macau University of Science and Technology, Macau, China.
Junning FengSchool of Computer Science and Engineering, Faculty of Innovation Engineering, Macau University of Science and Technology, Macau, China.
Shanghui LuSchool of Computer Science and Engineering, Faculty of Innovation Engineering, Macau University of Science and Technology, Macau, China.
Shuilin LiaoSchool of Computer Science and Engineering, Faculty of Innovation Engineering, Macau University of Science and Technology, Macau, China.
Xiaoying LiuComputer Engineering Technical College, Guangdong Polytechnic of Science and Technology, Zhuhai, China.
Shengli XieGuangdong-HongKong-Macao Joint Laboratory for Smart Discrete Manufacturing, Guangzhou, China.

Funding

Mathematics of the National Science Foundation of China 12326604Peng Cheng Laboratory PCL2023A09
6 · The paper itself

Abstract

Existing studies have shown that the abnormal expression of microRNAs (miRNAs) usually leads to the occurrence and development of human diseases. Identifying disease-related miRNAs contributes to studying the pathogenesis of diseases at the molecular level. As traditional biological experiments are time-consuming and expensive, computational methods have been used as an effective complement to infer the potential associations between miRNAs and diseases. However, most of the existing computational methods still face three main challenges: (i) learning of high-order relations; (ii) insufficient representation learning ability; (iii) importance learning and integration of multi-view embedding representation. To this end, we developed a HyperGraph Contrastive Learning with view-aware Attention Mechanism and Integrated multi-view Representation (HGCLAMIR) model to discover potential miRNA-disease associations. First, hypergraph convolutional network (HGCN) was utilized to capture high-order complex relations from hypergraphs related to miRNAs and diseases. Then, we combined HGCN with contrastive learning to improve and enhance the embedded representation learning ability of HGCN. Moreover, we introduced view-aware attention mechanism to adaptively weight the embedded representations of different views, thereby obtaining the importance of multi-view latent representations. Next, we innovatively proposed integrated representation learning to integrate the embedded representation information of multiple views for obtaining more reasonable embedding information. Finally, the integrated representation information was fed into a neural network-based matrix completion method to perform miRNA-disease association prediction. Experimental results on the cross-validation set and independent test set indicated that HGCLAMIR can achieve better prediction performance than other baseline models. Furthermore, the results of case studies and enrichment analysis further demonstrated the accuracy of HGCLAMIR and unconfirmed potential associations had biological significance.

Indexed as

Computational BiologyMicroRNAsAlgorithmsGenetic Predisposition to DiseaseHumansMachine LearningNeural Networks, ComputerMicroRNAs

Identifiers

PMID38652712
PMCPMC11037542

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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.