Evidence map›Paper›PMID 40346538›Full record

ArticleBMC biology2025

Leveraging explainable multi-scale features for fine-grained circRNA-miRNA interaction prediction.

Li Peng, Wang Wang, Zongyi Yang, Xiangzheng Fu, Wei Liang, Dongsheng Cao

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

6 authors.

Li PengSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, 411100, China. plpeng@hnu.edu.cn.
Wang WangSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, 411100, China.
Zongyi YangSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, 411100, China.
Xiangzheng FuCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, 410012, Hunan, China. fxz326@hnu.edu.cn.
Wei LiangSchool of Computer Science and Engineering, Hunan University of Science and Technology, Xiangtan, 411100, China.
Dongsheng CaoXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410003, Hunan, China.

Funding

National Natural Science Foundation of China Nos. 62372158, 62402533Natural Science Foundation of Hunan province No.2023JJ30264Scientific Research Project of Hunan Education Department Nos.22A0350, 23B0237,22C0267
6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs) and microRNAs (miRNAs) interactions have essential implications in various biological processes and diseases. Computational science approaches have emerged as powerful tools for studying and predicting these intricate molecular interactions, garnering considerable attention. Current methods face two significant limitations: the lack of precise interpretable models and insufficient representation of homogeneous and heterogeneous molecules.

resultsWe propose a novel method, MFERL, that addresses both limitations through multi-scale representation learning and an explainable fine-grained model for predicting circRNA-miRNA interactions (CMI). MFERL learns multi-scale representations by aggregating homogeneous node features and interacting with heterogeneous node features, as well as through novel dual-convolution attention mechanisms and contrastive learning to enhance features.

conclusionsWe utilize a manifold-based method to examine model performance in detail, revealing that MFERL exhibits robust generalization, robustness, and interpretability. Extensive experiments show that MFERL outperforms state-of-the-art models and offers a promising direction for understanding CMI intrinsic mechanisms.

Indexed as

Computational BiologyMicroRNAsRNA, CircularHumansMicroRNAsRNA, CircularcircRNAExplainabilitymiRNAMulti-scale featureRepresentation learning

Identifiers

PMID40346538
PMCPMC12065178

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.