Inferring miRNA-disease associations using collaborative filtering and resource allocation on a tripartite graph.

BACKGROUND: Developing efficient and successful computational methods to infer potential miRNA-disease associations is urgently needed and is attracting many computer scientists in recent years. The reason is that miRNAs are involved in many important biological processes and it is tremendously expensive and time-consuming to do biological experiments to verify miRNA-disease associations. METHODS: In this paper, we proposed a new method to infer miRNA-disease associations using collaborative filtering and resource allocation algorithms on a miRNA-disease-lncRNA tripartite graph. It combined the collaborative filtering algorithm in CFNBC model to solve the problem of imbalanced data and the method for association prediction established multiple types of known associations among multiple objects presented in TPGLDA model. RESULTS: The experimental results showed that our proposed method achieved a reliable performance with Area Under Roc Curve (AUC) and Area Under Precision-Recall Curve (AUPR) values of 0.9788 and 0.9373, respectively, under fivefold-cross-validation experiments. It outperformed than some other previous methods such as DCSMDA and TPGLDA. Furthermore, it demonstrated the ability to derive new associations between miRNAs and diseases among 8, 19 and 14 new associations out of top 40 predicted associations in case studies of Prostatic Neoplasms, Heart Failure, and Glioma diseases, respectively. All of these new predicted associations have been confirmed by recent literatures. Besides, it could discover new associations for new diseases (or miRNAs) without any known associations as demonstrated in the case study of Open-angle glaucoma disease. CONCLUSION: With the reliable performance to infer new associations between miRNAs and diseases as well as to discover new associations for new diseases (or miRNAs) without any known associations, our proposed method can be considered as a powerful tool to infer miRNA-disease associations.

A novel solution of using deep learning for left ventricle detection: Enhanced feature extraction.

BACKGROUND AND AIM: deep learning algorithms have not been successfully used for the left ventricle (LV) detection in echocardiographic images due to overfitting and vanishing gradient descent problem. This research aims to increase accuracy and improves the processing time of the left ventricle detection process by reducing the overfitting and vanishing gradient problem. METHODOLOGY: the proposed system consists of an enhanced deep convolutional neural network with an extra convolutional layer, and dropout layer to solve the problem of overfitting and vanishing gradient. Data augmentation was used for increasing the accuracy of feature extraction for left ventricle detection. RESULTS: four pathological groups of datasets were used for training and evaluation of the model: heart failure without infarction, heart failure with infarction, and hypertrophy, and healthy. The proposed model provided an accuracy of 94% in left ventricle detection for all the groups compared to the other current systems. The results showed that the processing time was reduced from 0.45 s to 0.34 s in an average. CONCLUSION: the proposed system enhances accuracy and decreases processing time in the left ventricle detection. This paper solves the issues of overfitting of the data.