Abstract
Recently, an increasing number of studies have demonstrated that miRNAs are involved in human diseases, indicating that miRNAs might be a potential pathogenic factor for various diseases. Therefore, figuring out the relationship between miRNAs and diseases plays a critical role in not only the development of new drugs, but also the formulation of individualized diagnosis and treatment. As the prediction of miRNA-disease association via biological experiments is expensive and time-consuming, computational methods have a positive effect on revealing the association. In this study, a novel prediction model integrating GCN, CNN and Squeeze-and-Excitation Networks (GCSENet) was constructed for the identification of miRNA-disease association. The model first captured features by GCN based on a heterogeneous graph including diseases, genes and miRNAs. Then, considering the different effects of genes on each type of miRNA and disease, as well as the different effects of the miRNA-gene and disease-gene relationships on miRNA-disease association, a feature weight was set and a combination of miRNA-gene and disease-gene associations was added as feature input for the convolution operation in CNN. Furthermore, the squeeze and excitation blocks of SENet were applied to determine the importance of each feature channel and enhance useful features by means of the attention mechanism, thus achieving a satisfactory prediction of miRNA-disease association. The proposed method was compared against other state-of-the-art methods. It achieved an AUROC score of 95.02% and an AUPR score of 95.55% in a 10-fold cross-validation, which led to the finding that the proposed method is superior to these popular methods on most of the performance evaluation indexes.
Highlights
MicroRNAs are a type of small non-coding RNAs (22~24 nucleotides in length), which function as an important regulator in human body [1]
We have verified the effects of graph convolutional network (GCN) module, feature weights, new feature component and SENet module, and found each component is beneficial to our prediction model, which are described of comparison with different GCSENet components
We evaluate the performance of GCSENet and other five methods (i.e., WBSMDA [8], path-based miRNA-disease association (PBMDA) [9], MDACNN [15], SAEMDA [10], NIMCGCN [16]) on the task of predicting miRNA-disease associations
Summary
MicroRNAs (miRNAs) are a type of small non-coding RNAs (22~24 nucleotides in length), which function as an important regulator in human body [1]. More and more studies have revealed that miRNA is closely related to human diseases, such as Parkinson’s disease [2] and cancer [3]. The identification of association between miRNAs and diseases is of great significance for the study on disease pathogenesis and the development of drugs. It is costly and time-consuming to identify the associations between a pair of miRNA and disease/ phenotype through biological experiment. The basic assumption is that the miRNAs associated with the same or similar diseases are more likely to be functionally related. The existing methods can be roughly divided into two categories: network based methods and machine learning based algorithms
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