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Prediction of Potential miRNA–Disease Associations Through a Novel Unsupervised Deep Learning Framework with Variational Autoencoder

机译:通过具有变分自动编码器的新型无监督深度学习框架预测潜在的miRNA-疾病关联

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摘要

The important role of microRNAs (miRNAs) in the formation, development, diagnosis, and treatment of diseases has attracted much attention among researchers recently. In this study, we present an unsupervised deep learning model of the variational autoencoder for MiRNA–disease association prediction (VAEMDA). Through combining the integrated miRNA similarity and the integrated disease similarity with known miRNA–disease associations, respectively, we constructed two spliced matrices. These matrices were applied to train the variational autoencoder (VAE), respectively. The final predicted association scores between miRNAs and diseases were obtained by integrating the scores from the two trained VAE models. Unlike previous models, VAEMDA can avoid noise introduced by the random selection of negative samples and reveal associations between miRNAs and diseases from the perspective of data distribution. Compared with previous methods, VAEMDA obtained higher area under the receiver operating characteristics curves (AUCs) of 0.9118, 0.8652, and 0.9091 ± 0.0065 in global leave-one-out cross validation (LOOCV), local LOOCV, and five-fold cross validation, respectively. Further, the AUCs of VAEMDA were 0.8250 and 0.8237 in global leave-one-disease-out cross validation (LODOCV), and local LODOCV, respectively. In three different types of case studies on three important diseases, the results showed that most of the top 50 potentially associated miRNAs were verified by databases and the literature.
机译:microRNA(miRNA)在疾病的形成,发展,诊断和治疗中的重要作用最近引起了研究人员的广泛关注。在这项研究中,我们提出了一种用于MiRNA-疾病关联预测(VAEMDA)的变分自动编码器的无监督深度学习模型。通过将整合的miRNA相似性和整合的疾病相似性分别与已知的miRNA-疾病关联相结合,我们构建了两个剪接矩阵。这些矩阵分别用于训练变分自动编码器(VAE)。通过整合来自两个训练有素的VAE模型的分数,可以获得miRNA与疾病之间的最终预测关联分数。与以前的模型不同,VAEMDA可以避免从阴性样本的随机选择中引入噪音,并从数据分布的角度揭示miRNA与疾病之间的关联。与以前的方法相比,VAEMDA在全局留一法交叉验证(LOOCV),局部LOOCV和五重交叉验证中,在接收器工作特性曲线(AUC)为0.9118、0.8652和0.9091±0.0065时获得了更大的面积,分别。此外,VAEMDA的AUC在全球遗留一病出交叉验证(LODOCV)和本地LODOCV中分别为0.8250和0.8237。在对三种重要疾病的三种不同类型的案例研究中,结果表明,数据库和文献均对前50个潜在相关的miRNA中的大多数进行了验证。

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