Graph-guided Bayesian SVM with Adaptive Structured Shrinkage Prior for High-dimensional Data.

Wenli Sun, Changgee Chang, Qi Long
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Abstract

Support vector machine (SVM) is a popular classification method for the analysis of a wide range of data including big biomedical data. Many SVM methods with feature selection have been developed under the frequentist regularization or Bayesian shrinkage frameworks. On the other hand, the value of incorporating a priori known biological knowledge, such as those from functional genomics and functional proteomics, into statistical analysis of -omic data has been recognized in recent years. Such biological information is often represented by graphs. We propose a novel method that assigns Laplace priors to the regression coefficients and incorporates the underlying graph information via a hyper-prior for the shrinkage parameters in the Laplace priors. This enables smoothing of shrinkage parameters for connected variables in the graph and conditional independence between shrinkage parameters for disconnected variables. Extensive simulations demonstrate that our proposed methods achieve the best performance compared to the other existing SVM methods in terms of prediction accuracy. The proposed method are also illustrated in analysis of genomic data from cancer studies, demonstrating its advantage in generating biologically meaningful results and identifying potentially important features.

高维数据自适应结构收缩先验的图导贝叶斯支持向量机。
支持向量机(SVM)是一种流行的分类方法,用于分析包括大型生物医学数据在内的广泛数据。在频率正则化或贝叶斯收缩框架下,已经开发了许多具有特征选择的SVM方法。另一方面,近年来,将先验的已知生物学知识,如功能基因组学和功能蛋白质组学的知识,纳入组学数据的统计分析中的价值已得到认可。这种生物信息通常用图表表示。我们提出了一种新的方法,该方法将拉普拉斯先验分配给回归系数,并通过拉普拉斯先验中收缩参数的超先验结合底层图信息。这样可以平滑图中连接变量的收缩参数,并使断开连接的变量收缩参数之间的条件独立性。大量仿真表明,与其他现有的SVM方法相比,我们提出的方法在预测精度方面实现了最佳性能。所提出的方法也在癌症研究的基因组数据分析中得到了说明,证明了其在产生有生物学意义的结果和识别潜在重要特征方面的优势。
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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