Evidence map›Paper›PMID 39127625›Full record

ArticleBMC bioinformatics2024

BEROLECMI: a novel prediction method to infer circRNA-miRNA interaction from the role definition of molecular attributes and biological networks.

Xin-Fei Wang, Chang-Qing Yu, Zhu-Hong You, Yan Wang, Lan Huang, Yan Qiao, Lei Wang, Zheng-Wei Li

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Xin-Fei WangSchool of Information Engineering, Xijing University, Xi'an, China.
Chang-Qing YuSchool of Information Engineering, Xijing University, Xi'an, China. xaycq@163.com.
Zhu-Hong YouSchool of Computer Science, Northwestern Polytechnical University, Xi'an, China. zhuhongyou@nwpu.edu.cn.
Yan WangKey Laboratory of Symbol Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun, China. wy6868@jlu.edu.cn.
Lan HuangKey Laboratory of Symbol Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun, China.
Yan QiaoCollege of Agriculture and Forestry, Longdong University, Qingyang, China.
Lei WangSchool of Computer Science and Technology, China University of Mining and Technology, Xuzhou, China.
Zheng-Wei LiSchool of Computer Science and Technology, China University of Mining and Technology, Xuzhou, China.

Funding

National Natural Science Foundation of China 62273284
6 · The paper itself

Abstract

Circular RNA (CircRNA)-microRNA (miRNA) interaction (CMI) is an important model for the regulation of biological processes by non-coding RNA (ncRNA), which provides a new perspective for the study of human complex diseases. However, the existing CMI prediction models mainly rely on the nearest neighbor structure in the biological network, ignoring the molecular network topology, so it is difficult to improve the prediction performance. In this paper, we proposed a new CMI prediction method, BEROLECMI, which uses molecular sequence attributes, molecular self-similarity, and biological network topology to define the specific role feature representation for molecules to infer the new CMI. BEROLECMI effectively makes up for the lack of network topology in the CMI prediction model and achieves the highest prediction performance in three commonly used data sets. In the case study, 14 of the 15 pairs of unknown CMIs were correctly predicted.

Indexed as

Computational BiologyMicroRNAsRNA, CircularAlgorithmsGene Regulatory NetworksHumansRNAMicroRNAsRNARNA, CircularAssociation predictionBiomarker discoverycircRNA–miRNA interactionCompeting endogenous RNANetwork embedding

Identifiers

PMID39127625
PMCPMC11316391

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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.