Three-Layer Heterogeneous Network Combined With Unbalanced Random Walk for miRNA-Disease Association Prediction

miRNA plays an important role in many biological processes, and increasing evidence shows that miRNAs are closely related to human diseases. Most existing miRNA-disease association prediction methods were only based on data related to miRNAs and diseases and failed to effectively use other existing...

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Veröffentlicht in:Frontiers in genetics 2020-01, Vol.10, p.1316-1316
Hauptverfasser: Yu, Limin, Shen, Xianjun, Zhong, Duo, Yang, Jincai
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Sprache:eng
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Zusammenfassung:miRNA plays an important role in many biological processes, and increasing evidence shows that miRNAs are closely related to human diseases. Most existing miRNA-disease association prediction methods were only based on data related to miRNAs and diseases and failed to effectively use other existing biological data. However, experimentally verified miRNA-disease associations are limited, there are complex correlations between biological data. Therefore, we propose a novel Three-layer heterogeneous network Combined with unbalanced Random Walk for MiRNA-Disease Association prediction algorithm (TCRWMDA), which can effectively integrate multi-source association data. TCRWMDA based not only on the known miRNA-disease associations, also add the new priori information (lncRNA-miRNA and lncRNA-disease associations) to build a three-layer heterogeneous network, lncRNA was added as the transition path of the intermediate point to mine more effective information between networks. The AUC value obtained by the TCRWMDA algorithm on 5-fold cross validation is 0.9209, compared with other models based on the same similarity calculation method, TCRWMDA obtained better results. TCRWMDA was applied to the analysis of four types of cancer, the results proved that TCRWMDA is an effective tool to predict the potential miRNA-disease association. The source code and dataset of TCRWMDA are available at: https://github.com/ylm0505/TCRWMDA.
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2019.01316