Deep matrix factorization improves prediction of human circRNA-disease associations

In recent years, more and more evidence indicates that circular RNAs (circRNAs) with covalently closed loop play various roles in biological processes. Dysregulation and mutation of circRNAs may be implicated in diseases. Due to its stable structure and resistance to degradation, circRNAs provide great potential to be diagnostic biomarkers. Therefore, predicting circRNA-disease associations is helpful in disease diagnosis. However, there are few experimentally validated associations between circRNAs and diseases. Although several computational methods have been proposed, precisely representing underlying features and grasping the complex structures of data are still challenging. In this paper, we design a new method, called DMFCDA (Deep Matrix Factorization CircRNA-Disease association), to infer potential circRNA-disease associations. DMFCDA takes both explicit and implicit feedback into account. Then, it uses a projection layer to automatically learn latent representations of circRNAs and diseases. With multi-layer neural networks, DMFCDA can model the non-linear associations to grasp the complex structure of data. We assess the performance of DMFCDA using leave-one cross-validation and 5-fold cross-validation on two datasets. Computational results show that DMFCDA efficiently infers circRNA-disease associations according to AUC values, the percentage of precisely retrieved associations in various top ranks, and statistical comparison. We also conduct case studies to evaluate DMFCDA. All results show that DMFCDA provides accurate predictions.