Evidence map›Paper›PMID 39623332›Full record

ArticleBMC genomics2024

Disentangled similarity graph attention heterogeneous biological memory network for predicting disease-associated miRNAs.

Yinbo Liu, Qi Wu, Le Zhou, Yuchen Liu, Chao Li, Zhuoyu Wei, Wei Peng, Yi Yue, Xiaolei Zhu

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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Yinbo Liu *School of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China.
Qi Wu *School of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China.
Le ZhouInstitute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Yuchen LiuInstitute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Chao LiInstitute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Zhuoyu WeiSchool of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China.
Wei PengSchool of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China.
Yi YueSchool of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China. yyyue@ahau.edu.cn.
Xiaolei ZhuSchool of Information and Artificial Intelligence, Anhui Agricultural University, Hefei, Anhui, 230036, China. xlzhu_mdl@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe association between MicroRNAs (miRNAs) and diseases is crucial in treating and exploring many diseases or cancers. Although wet-lab methods for predicting miRNA-disease associations (MDAs) are effective, they are often expensive and time-consuming. Significant advancements have been made using Graph Neural Network-based methods (GNN-MDAs) to address these challenges. However, these methods still face limitations, such as not considering nodes' deep-level similarity associations and hierarchical learning patterns. Additionally, current models do not retain the memory of previously learned heterogeneous historical information about miRNAs or diseases, only focusing on parameter learning without the capability to remember heterogeneous associations.

resultsThis study introduces the K-means disentangled high-level biological similarity to utilize potential hierarchical relationships fully and proposes a Graph Attention Heterogeneous Biological Memory Network architecture (DiGAMN) with memory capabilities. Extensive experiments were conducted across four datasets, comparing the DiGAMN model and its disentangling method against ten state-of-the-art non-disentangled methods and six traditional GNNs. DiGAMN excelled, achieving AUC scores of 96.35%, 96.10%, 96.01%, and 95.89% on the Data1 to Data4 datasets, respectively, surpassing all other models. These results confirm the superior performance of DiGAMN and its disentangling method. Additionally, various ablation studies were conducted to validate the contributions of different modules within the framework, and's encoding statuses and memory units of DiGAMN were visualized to explore the utility and functionality of its modules. Case studies confirmed the effectiveness of DiGAMN's predictions, identifying several new disease-associated miRNAs.

conclusionsDiGAMN introduces the use of a disentangled biological similarity approach for the first time and successfully constructs a Disentangled Graph Attention Heterogeneous Biological Memory Network model. This network can learn disentangled representations of similarity information and effectively store the potential biological entanglement information of miRNAs and diseases. By integrating disentangled similarity information with a heterogeneous attention memory network, DiGAMN enhances the model's ability to capture and utilize complex underlying biological data, significantly outperforming many existing models. The concepts used in this method also provide new perspectives for predicting miRNAs associated with diseases.

Indexed as

MicroRNAsAlgorithmsComputational BiologyGenetic Predisposition to DiseaseHumansNeural Networks, ComputerMicroRNAsDisentangled similarityHeterogeneous biological memory networkMDAs predictionMiRNA discovery

Identifiers

PMID39623332
PMCPMC11610307

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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.