Evidence map›Paper›PMID 38243694›Full record

ArticleBriefings in bioinformatics2023

MHCLMDA: multihypergraph contrastive learning for miRNA-disease association prediction.

Wei Peng, Zhichen He, Wei Dai, Wei Lan

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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  14. MicroRNA Gets a Mighty Award.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
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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

4 authors.

Wei PengFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Kunming, Yunnan 650500, P. R. China and Computer Technology Application Key Lab of Yunnan Province, Kunming University of Science and Technology, Kunming, Yunnan 650500, P. R. China.ORCID 0000-0002-9572-951X
Zhichen HeFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Kunming, Yunnan 650500, P. R. China.
Wei DaiFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Kunming, Yunnan 650500, P. R. China and Computer Technology Application Key Lab of Yunnan Province, Kunming University of Science and Technology, Kunming, Yunnan 650500, P. R. China.
Wei LanGuangxi Key Laboratory of Multimedia Communications and Network Technology, Guangxi University, Nanning 530004, China.ORCID 0000-0001-5839-7504

Funding

National Natural Science Foundation of China 61972185Natural Science Foundation of Yunnan Province of China 2019FA024Yunnan Ten Thousand Talents Plan
6 · The paper itself

Abstract

The correct prediction of disease-associated miRNAs plays an essential role in disease prevention and treatment. Current computational methods to predict disease-associated miRNAs construct different miRNA views and disease views based on various miRNA properties and disease properties and then integrate the multiviews to predict the relationship between miRNAs and diseases. However, most existing methods ignore the information interaction among the views and the consistency of miRNA features (disease features) across multiple views. This study proposes a computational method based on multiple hypergraph contrastive learning (MHCLMDA) to predict miRNA-disease associations. MHCLMDA first constructs multiple miRNA hypergraphs and disease hypergraphs based on various miRNA similarities and disease similarities and performs hypergraph convolution on each hypergraph to capture higher order interactions between nodes, followed by hypergraph contrastive learning to learn the consistent miRNA feature representation and disease feature representation under different views. Then, a variational auto-encoder is employed to extract the miRNA and disease features in known miRNA-disease association relationships. Finally, MHCLMDA fuses the miRNA and disease features from different views to predict miRNA-disease associations. The parameters of the model are optimized in an end-to-end way. We applied MHCLMDA to the prediction of human miRNA-disease association. The experimental results show that our method performs better than several other state-of-the-art methods in terms of the area under the receiver operating characteristic curve and the area under the precision-recall curve.

Indexed as

MicroRNAsAlgorithmsComputational BiologyHumansROC CurveMicroRNAshypergraph contrastive learninghypergraph convolutionMiRNA–disease association predictionmultiomics data fusionmultiview learning

Identifiers

PMID38243694
PMCPMC10796254

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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.