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Incorporating predictor network in penalized regression with application to microarray data.

机译:将预测因子网络纳入惩罚回归中,并应用于微阵列数据。

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摘要

We consider penalized linear regression, especially for "large p, small n" problems, for which the relationships among predictors are described a priori by a network. A class of motivating examples includes modeling a phenotype through gene expression profiles while accounting for coordinated functioning of genes in the form of biological pathways or networks. To incorporate the prior knowledge of the similar effect sizes of neighboring predictors in a network, we propose a grouped penalty based on the L(gamma)-norm that smoothes the regression coefficients of the predictors over the network. The main feature of the proposed method is its ability to automatically realize grouped variable selection and exploit grouping effects. We also discuss effects of the choices of the gamma and some weights inside the L(gamma)-norm. Simulation studies demonstrate the superior finite-sample performance of the proposed method as compared to Lasso, elastic net, and a recently proposed network-based method. The new method performs best in variable selection across all simulation set-ups considered. For illustration, the method is applied to a microarray dataset to predict survival times for some glioblastoma patients using a gene expression dataset and a gene network compiled from some Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways.
机译:我们考虑惩罚线性回归,特别是对于“大p,小n”问题,通过网络先验地描述了预测变量之间的关系。一类激励性的例子包括通过基因表达谱对表型建模,同时考虑生物途径或网络形式的基因的协调功能。为了合并网络中相邻预测变量的相似影响大小的先验知识,我们提出了基于L(γ)范数的分组惩罚,该惩罚对网络上的预测变量的回归系数进行了平滑处理。该方法的主要特点是能够自动实现分组变量选择和利用分组效果。我们还将讨论选择伽玛的影响以及L(伽玛)范数内的一些权重。仿真研究表明,与套索,弹性网和最近提出的基于网络的方法相比,该方法具有更好的有限样本性能。在考虑的所有模拟设置中,新方法在变量选择方面表现最佳。为了说明,该方法被应用到微阵列数据集上,使用基因表达数据集和从《京都议定书》的基因和基因组百科全书(KEGG)途径汇编的基因网络,预测某些胶质母细胞瘤患者的生存时间。

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