Bayesian Non-Parametric Mixture Model with Application to Modeling Biological Markers

M. K. Peter, L. Mbugua, A. Wanjoya
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引用次数: 0

Abstract

The effect of treatment on patient’s outcome can easily be determined through the impact of the treatment on biological events. Observing the treatment for patients for a certain period of time can help in determining whether there is any change in the biomarker of the patient. It is important to study how the biomarker changes due to treatment and whether for different individuals located in separate centers can be clustered together since they might have different distributions. The study is motivated by a Bayesian non-parametric mixture model, which is more flexible when compared to the Bayesian Parametric models and is capable of borrowing information across different centers allowing them to be grouped together. To this end, this research modeled Biological markers taking into consideration the Surrogate markers. The study employed the nested Dirichlet process prior, which is easily peaceable on different distributions for several centers, with centers from the same Dirichlet process component clustered automatically together. The study sampled from the posterior by use of Markov chain Monte carol algorithm. The model is illustrated using a simulation study to see how it performs on simulated data. Clearly, from the simulation study it was clear that, the model was capable of clustering data into different clusters.
贝叶斯非参数混合模型及其在生物标记建模中的应用
通过治疗对生物事件的影响,可以很容易地确定治疗对患者结局的影响。观察患者的治疗一段时间可以帮助确定患者的生物标志物是否有任何变化。重要的是研究生物标志物如何因治疗而变化,以及位于不同中心的不同个体是否可以聚集在一起,因为它们可能具有不同的分布。这项研究的动机是贝叶斯非参数混合模型,与贝叶斯参数模型相比,该模型更灵活,能够跨不同中心借用信息,从而将它们分组在一起。为此,本研究对生物标记物进行了建模,并考虑了代孕标记物。该研究采用了嵌套的狄利克雷过程先验,它在几个中心的不同分布上很容易和平,来自同一狄利克雷进程组件的中心自动聚集在一起。本研究采用马尔可夫链蒙特卡罗算法从后验样本中抽取样本。通过模拟研究对该模型进行了说明,以了解其在模拟数据上的表现。显然,从模拟研究中可以清楚地看出,该模型能够将数据聚类到不同的聚类中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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