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Maximal entropy random walk on heterogenous network for MIRNA-disease Association prediction
Ya-Wei Niu1, Hua Liu1, Guang-Hui Wang1
1School of Mathematics, Shandong University, Jinan 250100, China.
Mathematical Biosciences
|October 19, 2018
Summary
This study introduces MERWMDA, a computational model using Maximal Entropy Random Walk on a heterogeneous network to predict microRNA-disease associations. MERWMDA accurately identifies potential links, offering valuable candidates for biomedical research.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- MicroRNAs (miRNAs) play crucial roles in human disease development.
- Predicting disease-miRNA associations is of increasing interest.
- Existing in silico models leverage publicly available miRNA databases.
Purpose of the Study:
- To develop a computational model for predicting potential disease-miRNA associations.
- To integrate diverse biological data into a heterogeneous network for enhanced prediction.
- To validate the model's performance through cross-validation and case studies.
Main Methods:
- Developed the Maximal Entropy Random Walk on heterogeneous network for MiRNA-disease Association prediction (MERWMDA) model.
- Constructed a heterogeneous network integrating known disease-miRNA associations, miRNA functional relations, and disease semantic relations.
- Applied Maximal Entropy Random Walk (MERW) on the network to identify potential associations.
Main Results:
- MERWMDA achieved high performance in cross-validation, with AUCs of 0.8966 (global) and 0.8491 (local).
- Case studies on Esophageal cancer and Prostate cancer showed high confirmation rates (94% and 88%) for top-ranked miRNAs.
- Validation on Lung cancer and Lymphoma demonstrated the model's robustness and predictive power for novel associations.
Conclusions:
- MERWMDA is an effective computational tool for predicting disease-miRNA associations.
- The model provides valuable candidate miRNAs for further experimental validation.
- This approach can aid in understanding disease mechanisms and identifying potential therapeutic targets.
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