Zeng Yaohui, Breheny Patrick
Department of Biostatistics, University of Iowa, Iowa City, IA, USA.
Cancer Inform. 2016 Sep 15;15:179-87. doi: 10.4137/CIN.S40043. eCollection 2016.
Discovering important genes that account for the phenotype of interest has long been a challenge in genome-wide expression analysis. Analyses such as gene set enrichment analysis (GSEA) that incorporate pathway information have become widespread in hypothesis testing, but pathway-based approaches have been largely absent from regression methods due to the challenges of dealing with overlapping pathways and the resulting lack of available software. The R package grpreg is widely used to fit group lasso and other group-penalized regression models; in this study, we develop an extension, grpregOverlap, to allow for overlapping group structure using a latent variable approach. We compare this approach to the ordinary lasso and to GSEA using both simulated and real data. We find that incorporation of prior pathway information can substantially improve the accuracy of gene expression classifiers, and we shed light on several ways in which hypothesis-testing approaches such as GSEA differ from regression approaches with respect to the analysis of pathway data.
长期以来,在全基因组表达分析中,发现导致感兴趣表型的重要基因一直是一项挑战。诸如基因集富集分析(GSEA)等纳入通路信息的分析方法在假设检验中已广泛应用,但由于处理重叠通路存在挑战且缺乏可用软件,基于通路的方法在回归方法中基本未被采用。R包grpreg被广泛用于拟合组套索和其他组惩罚回归模型;在本研究中,我们开发了一个扩展包grpregOverlap,通过潜在变量方法允许使用重叠组结构。我们使用模拟数据和真实数据将此方法与普通套索和GSEA进行比较。我们发现纳入先验通路信息可显著提高基因表达分类器的准确性,并且我们阐明了在通路数据分析方面,诸如GSEA等假设检验方法与回归方法不同的几种方式。