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Screening of miRNA target genes in coronary artery disease by variational Bayesian Gaussian mixture model

机译:应用变分贝叶斯高斯混合模型筛选冠心病的miRNA靶基因。

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摘要

Coronary artery disease (CAD) is a leading cause of death, and microRNAs (miRNAs) are widely involved in physiological and pathological processes of CAD. We chose the targetscore method calculated via the variational Bayesian Gaussian mixture model (VB-GMM) as the prediction method of target genes. By observing the density overlap, we selected the thresholds of miRNA-1 and miRNA-155. In total, 18 target genes of miRNA-1, and 19 target genes of miRNA-155 were identified. The threshold of miRNA-146a was selected using the |logFC| value, and 16 target genes were screened out. In this study, our major contribution was to predict the target messenger RNAs (mRNAs) of the chosen miRNAs with the gene expression profiles, which can effectively reduce the workload of screening. Although the validated genes constituted only a small part in the final prediction results, it is a good sign for research in the future. It means that we could provide new research aims for future studies focusing on miRNA regulatory mechanisms.
机译:冠状动脉疾病(CAD)是导致死亡的主要原因,microRNA(miRNA)广泛参与CAD的生理和病理过程。我们选择通过变分贝叶斯高斯混合模型(VB-GMM)计算的targetcore方法作为目标基因的预​​测方法。通过观察密度重叠,我们选择了miRNA-1和miRNA-155的阈值。总共鉴定出18个miRNA-1靶基因和19个miRNA-155靶基因。使用| logFC |选择miRNA-146a的阈值。值,并筛选出16个靶基因。在这项研究中,我们的主要贡献是通过基因表达谱预测所选miRNA的目标信使RNA(mRNA),可以有效减少筛选工作量。尽管经过验证的基因仅占最终预测结果的一小部分,但这是未来研究的一个好兆头。这意味着我们可以为今后针对miRNA调控机制的研究提供新的研究目标。

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