Evidence map›Paper›PMID 42056851›Full record

ArticleBMC bioinformatics2026

Multi-granularity transformer contrastive learning and feature reconstruction for prediction of disease-related miRNAs.

Ping Xuan, Zhicheng Guo, Siyuan Lu, Hui Cui, Jian Ding, Tiangang Zhang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. 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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ping XuanSchool of Cyberspace Security, Hainan University, Haikou, 570228, China. pingxuan@hainanu.edu.cn.
Zhicheng GuoDepartment of Computer Science and Technology, Shantou University, Shantou, 515063, China.
Siyuan LuSchool of Computer Science and Technology, Heilongjiang University, Harbin, 150080, China.
Hui CuiDepartment of Computer Science and Information Technology, La Trobe University, Melbourne, 3083, Australia.
Jian DingHarbin Conservatory of Music, Harbin, 150028, China.
Tiangang ZhangSchool of Cyberspace Security, Hainan University, Haikou, 570228, China. zhangtg@hainanu.edu.cn.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2024A1515010176Natural Science Foundation of China 62372282Natural Science Foundation of Heilongjiang Province LH2023F044STU Scientific Research Initiation Grant NTF22032
6 · The paper itself

Abstract

The increasing research confirms the function of microRNAs (miRNAs) play a vital role in the diagnosis, treatment, and prognosis of diseases. Screening the potential candidate miRNAs related to the diseases by the computational methods may be helpful for reducing the experimental cost for discovering the actual disease-miRNA associations. Most of the recent methods exploited the data from multiple sources to infer the association tendencies between miRNAs and diseases. However, these methods did not completely learn the features of the multi-source data from multiple granularities. This paper present an association prediction model based on multi-granularity transformer contrastive learning and feature reconstruction convolution (APMF). First, the strongly correlated node sequences are constructed by random walks, and then the features of the positive and negative node sequences for the target node are learned. Second, the multi-granularity transformer strategy is designed to refine the features of the miRNA, disease, and lncRNA nodes from fine-granularity and coarse-granularity, respectively. Third, the contrastive learning strategy is presented to maximize the consistency among the features of positive samples and the difference among the features of positive samples and negative ones. Finally, the feature reconstruction convolution is constructed to capture the diverse semantics of features and suppress the noises of the data. The experimental results indicate that APMF outperforms several state-of-the-art methods for prediction of disease-related miRNAs. The ablation experiments demonstrate the effectiveness of the multi-granularity transformer contrastive learning and the feature reconstruction convolution. The case analysis over three diseases also shows APMF’s ability in discovering the potential miRNA candidates for the diseases.

Indexed as

Computational BiologyMachine LearningMicroRNAsAlgorithmsHumansRNA, Long NoncodingMicroRNAsRNA, Long NoncodingAttributes of multiple types of nodesDynamic attribute learning of hyperedgesDynamic topology formulation of hypergraphEncoding association characteristics among multiple lncRNAs and diseasesPairwise attribute learning enhanced by gated CNN

Identifiers

PMID42056851
PMCPMC13270722

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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.