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Discovery of miR-mRNA interactions via simultaneous Bayesian inference of gene networks and clusters using sequence-based predictions and expression data

机译:使用基于序列的预测和表达数据的基因网络和集群同时贝叶斯推断发现miR-mRNA相互作用

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Summary MicroRNAs (miRs) are known to interfere with mRNA expression, and much work has been put into predicting and inferring miR-mRNA interactions. Both sequence-based interaction predictions as well as interaction inference based on expression data have been proven somewhat successful; furthermore, models that combine the two methods have had even more success. In this paper, I further refine and enrich the methods of miR-mRNA interaction discovery by integrating a Bayesian clustering algorithm into a model of prediction-enhanced miR-mRNA target inference, creating an algorithm called PEACOAT, which is written in the R language. I show that PEACOAT improves the inference of miR-mRNA target interactions using both simulated data and a data set of microarrays from samples of multiple myeloma patients. In simulated networks of 25 miRs and mRNAs, our methods using clustering can improve inference in roughly two-thirds of cases, and in the multiple myeloma data set, KEGG pathway enrichment was found to be more significant with clustering than without. Our findings are consistent with previous work in clustering of non-miR genetic networks and indicate that there could be a significant advantage to clustering of miR and mRNA expression data as a part of interaction inference.
机译:众所周知MicroRNA(MIRS)会干扰mRNA表达,并且已经进入有很多工作预测和推断miR-mRNA相互作用。基于序列的交互预测以及基于表达数据的交互推断已经证明已经成功了;此外,组合这两种方法的模型也取得了成功。在本文中,我通过将贝叶斯聚类算法集成到预测增强的miR-mRNA目标推断模型中,进一步优化并丰富miR-mRNA交互发现的方法,从而创建一个名为peacoat的算法,该算法以R语言编写。我表明,PeacoAT通过两种骨髓瘤患者的样本改善了使用模拟数据和微阵列的微阵列的数据集的推理。在25 miRS和MRNA的模拟网络中,我们使用聚类的方法可以在大约三分之二的病例中提高推理,并且在多个骨髓瘤数据集中,被发现浓缩群体与聚类更为显着。我们的研究结果与以前的非MIR遗传网络聚类的工作一致,并表明将miR和mRNA表达数据聚类可能是相互作用推理的一部分的显着优势。

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