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Potential miRNA-disease association prediction based on kernelized Bayesian matrix factorization

机译:基于内核化贝叶斯矩阵分解的潜在miRNA-疾病关联预测

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Many biological experimental studies have confirmed that microRNAs (miRNAs) play a significant role in human complex diseases. Exploring miRNA-disease associations could be conducive to understanding disease pathogenesis at the molecular level and developing disease diagnostic biomarkers. However, since conducting traditional experiments is a costly and time-consuming way, plenty of computational models have been proposed to predict miRNA-disease associations. In this study, we presented a neoteric Bayesian model (KBMFMDA) that combines kernel-based nonlinear dimensionality reduction, matrix factorization and binary classification. The main idea of KBMFMDA is to project miRNAs and diseases into a unified subspace and estimate the association network in that subspace. KBMFMDA obtained the AUCs of 0.9132, 0.8708, 0.9008±0.0044 in global and local leave-one-out and five-fold cross validation. Moreover, KBMFMDA was applied to three important human cancers in three different kinds of case studies and most of the top 50 potential disease-related miRNAs were confirmed by many experimental reports.
机译:许多生物实验研究证实微大RNA(miRNA)在人类复杂疾病中起着重要作用。探索miRNA疾病协会可能有利于在分子水平和发育疾病诊断生物标志物中了解疾病发病机制。然而,由于进行传统实验是一种昂贵且耗时的方式,已经提出了大量的计算模型来预测MiRNA-疾病协会。在这项研究中,我们介绍了一个新的贝叶斯模型(KBMFMDA),它结合了基于内核的非线性维度降低,矩阵分解和二进制分类。 KBMFMDA的主要思想是将MiRNA和疾病预测到统一的子空间中,并估计该子空间中的关联网络。 KBMFMDA获得0.9132,0.8708,0.9008±0.0044的AUC,在全球和地方休假和五倍的交叉验证中。此外,KBMFMDA应用于三种不同的案例研究中的三种重要人类癌症,并且许多实验报告证实了大部分前50个潜在的疾病相关的miRNA。

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