Evidence map›Paper›PMID 35903359›Full record

ArticleFrontiers in genetics2022

Application of Bidirectional Generative Adversarial Networks to Predict Potential miRNAs Associated With Diseases.

Long Xu, Xiaokun Li, Qiang Yang, Long Tan, Qingyuan Liu, Yong Liu

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In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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5 · Who and what money

Authors and funding

6 authors.

Long XuSchool of Computer Science and Technology, Heilongjiang University, Harbin, China.
Xiaokun LiSchool of Computer Science and Technology, Heilongjiang University, Harbin, China.
Qiang YangSchool of Electronic Engineering, Heilongjiang University, Harbin, China.
Long TanSchool of Computer Science and Technology, Heilongjiang University, Harbin, China.
Qingyuan LiuPostdoctoral Program of Heilongjiang Hengxun Technology Co., Ltd., Heilongjiang University, Harbin, China.
Yong LiuSchool of Computer Science and Technology, Heilongjiang University, Harbin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Substantial evidence has shown that microRNAs are crucial for biological processes within complex human diseases. Identifying the association of miRNA-disease pairs will contribute to accelerating the discovery of potential biomarkers and pathogenesis. Researchers began to focus on constructing computational models to facilitate the progress of disease pathology and clinical medicine by identifying the potential disease-related miRNAs. However, most existing computational methods are expensive, and their use is limited to unobserved relationships for unknown miRNAs (diseases) without association information. In this manuscript, we proposed a creatively semi-supervised model named bidirectional generative adversarial network for miRNA-disease association prediction (BGANMDA). First, we constructed a microRNA similarity network, a disease similarity network, and Gaussian interaction profile kernel similarity based on the known miRNA-disease association and comprehensive similarity of miRNAs (diseases). Next, an integrated similarity feature network with the full underlying relationships of miRNA-disease pairwise was obtained. Then, the similarity feature network was fed into the BGANMDA model to learn advanced traits in latent space. Finally, we ranked an association score list and predicted the associations between miRNA and disease. In our experiment, a five-fold cross validation was applied to estimate BGANMDA's performance, and an area under the curve (AUC) of 0.9319 and a standard deviation of 0.00021 were obtained. At the same time, in the global and local leave-one-out cross validation (LOOCV), the AUC value and standard deviation of BGANMDA were 0.9116 ± 0.0025 and 0.8928 ± 0.0022, respectively. Furthermore, BGANMDA was employed in three different case studies to validate its prediction capability and accuracy. The experimental results of the case studies showed that 46, 46, and 48 of the top 50 prediction lists had been identified in previous studies.

Indexed as

bidirectional generative adversarial networkcomplex diseasemicroRNAsMiRNA–disease association predictionsimilarity network

Identifiers

PMID35903359
PMCPMC9314862

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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 Socratic graph.