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EPMDA: Edge Perturbation Based Method for miRNA-Disease Association Prediction

机译:EPMDA:基于边缘扰动的miRNA疾病协会预测方法

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In the recent few years, plenty of research has shown that microRNA (miRNA) is likely to be involved in the formation of many human diseases. So effectively predicting potential associations between miRNAs and diseases helps to understand the development and treatment of diseases. In this study, an edge perturbation based method is proposed for predicting potential miRNA-disease association (EPMDA). Different from the previous studies, we design an feature vector to describe each edge of a graph by structural Hamiltonian information. Moreover, the extracted features are used to train a multi-layer perception model to predict the candidate disease-miRNA associations. The experimental results on the HMDD dataset show that EPMDA achieves the AUC value of 0.9818 through 5-fold cross-validation, which improves the AUC values by approximately 3.5 percent compared to the latest method DeepMDA. For the leave-one-disease-out cross-validation, EPMDA achieves the AUC value of 0.9371, which improves the AUC values by approximately 7.4 percent compared to DeepMDA. In the case study, we verify the prediction performance of EPMDA on three human diseases. As a result, there are 42, 46, and 41 of the top 50 predicted miRNAs for these three diseases which are confirmed by the published experimental discoveries, respectively.
机译:在近年来几年中,大量的研究表明,MicroRNA(miRNA)可能会参与许多人类疾病的形成。因此,有效地预测MiRNA和疾病之间的潜在关联有助于了解疾病的发展和治疗。在该研究中,提出了一种基于边缘扰动的方法,用于预测潜在的miRNA疾病协会(EPMDA)。与以前的研究不同,我们设计了一个特征向量,通过结构哈密顿信息来描述图的每个边缘。此外,提取的特征用于训练多层感知模型以预测候选疾病 - miRNA关联。 HMDD数据集的实验结果表明,EPMDA通过5倍交叉验证实现0.9818的AUC值,与最新方法DeepMDA相比将AUC值提高了约3.5%。对于休假 - 单疾病交叉验证,EPMDA实现了0.9371的AUC值,而与DeepMDA相比将AUC值提高约7.4%。在案例研究中,我们验证了EPMDA对三种人类疾病的预测性能。结果,对于这三种疾病,前50个预测的miRNA的42,46和41分别由公开的实验发现确认。

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