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SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost

机译:Smalf:基于堆叠的AutoEncoder和XGBoost的miRNA-疾病关联预测

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Identifying miRNA and disease associations helps us understand disease mechanisms of action from the molecular level. However, it is usually blind, time-consuming, and small-scale based on biological experiments. Hence, developing computational methods to predict unknown miRNA and disease associations is becoming increasingly important. In this work, we develop a computational framework called SMALF to predict unknown miRNA-disease associations. SMALF first utilizes a stacked autoencoder to learn miRNA latent feature and disease latent feature from the original miRNA-disease association matrix. Then, SMALF obtains the feature vector of representing miRNA-disease by integrating miRNA functional similarity, miRNA latent feature, disease semantic similarity, and disease latent feature. Finally, XGBoost is utilized to predict unknown miRNA-disease associations. We implement cross-validation experiments. Compared with other state-of-the-art methods, SAMLF achieved the best AUC value. We also construct three case studies, including hepatocellular carcinoma, colon cancer, and breast cancer. The results show that 10, 10, and 9 out of the top ten predicted miRNAs are verified in MNDR v3.0 or miRCancer, respectively. The comprehensive experimental results demonstrate that SMALF is effective in identifying unknown miRNA-disease associations.
机译:鉴定miRNA和疾病关联有助于我们了解从分子水平的疾病作用的疾病机制。然而,基于生物实验通常是盲目,耗时和小规模的。因此,制定预测未知miRNA和疾病协会的计算方法变得越来越重要。在这项工作中,我们开发了一种称为Smalf的计算框架,以预测未知的miRNA疾病协会。 Smalf首先利用堆叠的AutoEncoder从原始miRNA-疾病协会基质中学习miRNA潜在特征和疾病潜在特征。然后,通过将MiRNA功能相似性,miRNA潜在,疾病语义相似性和疾病潜在特征集成MiRNA功能相似性,Smalf获得代表miRNA疾病的特征载体。最后,利用XGBoost预测未知的miRNA疾病协会。我们实施交叉验证实验。与其他最先进的方法相比,SAMLF实现了最佳的AUC值。我们还构建了三种案例研究,包括肝细胞癌,结肠癌和乳腺癌。结果表明,在MNDR v3.0或MiRcancer中验证了10,10和9中的前十个预测的miRNA。综合实验结果表明,Smalf在鉴定未知的miRNA疾病关联方面是有效的。

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