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BAYESIAN SPARSE GRAPHICAL MODELS FOR CLASSIFICATION WITH APPLICATION TO PROTEIN EXPRESSION DATA

机译:贝叶斯稀疏图形模型的分类及其在蛋白质表达数据中的应用

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Reverse-phase protein array (RPPA) analysis is a powerful, relatively new platform that allows for high-throughput, quantitative analysis of protein networks. One of the challenges that currently limit the potential of this technology is the lack of methods that allow for accurate data modeling and identification of related networks and samples. Such models may improve the accuracy of biological sample classification based on patterns of protein network activation and provide insight into the distinct biological relationships underlying different types of cancer. Motivated by RPPA data, we propose a Bayesian sparse graphical modeling approach that uses selection priors on the conditional relationships in the presence of class information. The novelty of our Bayesian model lies in the ability to draw information from the network data as well as from the associated categorical outcome in a unified hierarchical model for classification. In addition, our method allows for intuitive integration of a priori network information directly in the model and allows for posterior inference on the network topologies both within and between classes. Applying our methodology to an RPPA data set generated from panels of human breast cancer and ovarian cancer cell lines, we demonstrate that the model is able to distinguish the different cancer cell types more accurately than several existing models and to identify differential regulation of components of a critical signaling network (the PI3K-AKT pathway) between these two types of cancer. This approach represents a powerful new tool that can be used to improve our understanding of protein networks in cancer.
机译:反相蛋白质阵列(RPPA)分析是功能强大且相对较新的平台,可对蛋白质网络进行高通量的定量分析。当前限制该技术潜力的挑战之一是缺乏允许精确数据建模以及相关网络和样本识别的方法。这样的模型可以基于蛋白质网络激活的模式提高生物样品分类的准确性,并提供对不同类型癌症潜在的独特生物学关系的洞察力。受RPPA数据的启发,我们提出了一种贝叶斯稀疏图形建模方法,该方法在存在类信息的情况下对条件关系使用选择先验。贝叶斯模型的新颖之处在于能够从网络数据以及在用于分类的统一层次模型中从相关的分类结果中提取信息。此外,我们的方法允许直接在模型中直观集成先验网络信息,并允许在类内和类之间对网络拓扑进行后验推断。将我们的方法应用于从人类乳腺癌和卵巢癌细胞系面板生成的RPPA数据集,我们证明该模型比几种现有模型能够更准确地区分不同的癌细胞类型,并能够识别不同成分的调控。这两类癌症之间的关键信号网络(PI3K-AKT途径)。这种方法代表了一种强大的新工具,可用于增进我们对癌症中蛋白质网络的了解。

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