Abstract

Due to the cost and complexity of biological experiments, many computational methods have been proposed to predict potential miRNA-disease associations by utilizing known miRNA-disease associations and other related information. However, there are some challenges for these computational methods. First, the relationships between miRNAs and diseases are complex. The computational network should consider the local and global influence of neighborhoods from the network. Furthermore, predicting disease-related miRNAs without any known associations is also very important. This study presents a new computational method that constructs a heterogeneous network composed of a miRNA similarity network, disease similarity network, and known miRNA-disease association network. The miRNA similarity considers the miRNAs and their possible families and clusters. The information of each node in heterogeneous network is obtained by aggregating neighborhood information with graph convolutional networks (GCNs), which can pass the information of a node to its intermediate and distant neighbors. Disease-related miRNAs with no known associations can be predicted with the reconstructed heterogeneous matrix. We apply 5-fold cross-validation, leave-one-disease-out cross-validation, and global and local leave-one-out cross-validation to evaluate our method. The corresponding areas under the curves (AUCs) are 0.9616, 0.9946, 0.9656, and 0.9532, confirming that our approach significantly outperforms the state-of-the-art methods. Case studies show that this approach can effectively predict new diseases without any known miRNAs.

Highlights

  • MicroRNAs are a class of short non-coding single-stranded RNA molecules (22 nt) encoded by endogenous genes (Ambros, 2001)

  • Machine learning and matrix completion, we developed a matrix completion method based on graph convolutional networks for miRNA-disease association prediction

  • Considering the uniqueness and limitedness of available miRNA and disease samples, we implemented leave-one-out cross-validation (LOOCV), leave-onedisease-out cross-validation (LODOCV), and 5fold cross-validation to evaluate the performance of our method (Jiao and Du, 2016)

Read more

Summary

Introduction

MicroRNAs (miRNAs) are a class of short non-coding single-stranded RNA molecules (22 nt) encoded by endogenous genes (Ambros, 2001). Studies have shown that miRNAs are involved in the emergence and development of various human diseases (Alvarez-Garcia and Miska, 2005; Jopling et al, 2005). Finding the associations between miRNAs and diseases could contribute to pathological classifications, individualized diagnoses, and disease treatments. Experimental methods for identifying associations between miRNAs and diseases are expensive and timeconsuming. Computational methods have drawn wide attention to reveal potential associations between miRNAs and diseases. Based on the known miRNA-disease associations, a number of computational methods have been proposed to predict candidate miRNAs for diseases. These methods cover three main categories: network algorithms, machine learning, and matrixbased methods

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call