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Deep belief network–Based Matrix Factorization Model for MicroRNA-Disease Associations Prediction

机译:基于深度信仰网络的MicroRNA-疾病关联预测矩阵分解模型

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MicroRNAs (miRNAs) are small single-stranded noncoding RNAs that have shown to play a critical role in regulating gene expression. In past decades, cumulative experimental studies have verified that miRNAs are implicated in many complex human diseases and might be potential biomarkers for various types of diseases. With the increase of miRNA-related data and the development of analysis methodologies, some computational methods have been developed for predicting miRNA-disease associations, which are more economical and time-saving than traditional biological experimental approaches. In this study, a novel computational model, deep belief network (DBN)-based matrix factorization (DBN-MF), is proposed for miRNA-disease association prediction. First, the raw interaction features of miRNAs and diseases were obtained from the miRNA-disease adjacent matrix. Second, 2 DBNs were used for unsupervised learning of the features of miRNAs and diseases, respectively, based on the raw interaction features. Finally, a classifier consisting of 2 DBNs and a cosine score function was trained with the initial weights of DBN from the last step. During the training, the miRNA-disease adjacent matrix was factorized into 2 feature matrices for the representation of miRNAs and diseases, and the final prediction label was obtained according to the feature matrices. The experimental results show that the proposed model outperforms the state-of-the-art approaches in miRNA-disease association prediction based on the 10-fold crossvalidation. Besides, the effectiveness of our model was further demonstrated by case studies.
机译:MicroRNAs(miRNA)是小单链非致rNA,其显示在调节基因表达中起着关键作用。在过去的几十年中,累积的实验研究已经证实,miRNA涉及许多复杂的人类疾病,并且可能是各种类型的疾病的潜在生物标志物。随着MiRNA相关数据的增加和分析方法的发展,已经开发了一些用于预测MiRNA疾病关联的计算方法,这比传统的生物实验方法更经济和节省时间。在该研究中,提出了一种新的计算模型,基于基质分解(DBN-MF)的深度信念网络(DBN-MF),用于miRNA疾病关联预测。首先,从miRNA疾病相邻基质中获得miRNA和疾病的原始相互作用特征。其次,基于原始交互特征,分别用于分别用于分别为麦芽群和疾病特征的无监督学习。最后,由2个DBN和余弦分数函数组成的分类器,从最后一步中训练了DBN的初始权重。在训练期间,将相邻基质的miRNA-疾病被修理为2个特征基质,用于表示miRNA和疾病的表示,并且根据特征基质获得最终预测标签。实验结果表明,基于10倍的交叉验光,所提出的模型优于MiRNA疾病关联预测中的最先进方法。此外,通过案例研究进一步证明了我们模型的有效性。

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