Classification of Trends in Dose-Response Microarray Experiments Using Information Theory Selection Methods~!2009-02-24~!2009-07-09~!2009-12-23~!

Dan Lin, Z. Shkedy, T. Burzykowski, M. Aerts, Hinrich W. H. Göhlmann, A. Bondt, Tim Perera, T. Geerts, I. V. D. Wyngaert, L. Bijnens
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引用次数: 7

Abstract

Dose-response microarray experiments consist of monitoring expression levels of thousands of genes with respect to increasing dose of the treatment under investigation. The primary goal of such an experiment is to establish a dose-response relationship, while the secondary goals are to determine the minimum effective dose level and to identify the shape of the dose-response curve. Recently, Lin et al. (1) discussed several testing procedures to test for monotone trend based on isotonic regression of the observed means (2,3). Once a monotone relationship between the gene expression and dose is established, there is a set of R possible monotone models that can be fitted to the data. A selection of the best model from this set allows us to identify both the shape of dose-response curve and the minimum effective dose level. In this paper we focus on classification of dose-response curve shapes using the information theory model selection. In particular, the Order Restricted Information Criterion (ORIC) is discussed for the inference under order restriction. The posterior probability of the model is calculated using information criteria that take into account both the goodness-of-fit and the complexity of the models. The method is applied to a dose-response microarray experiment with 12 arrays (for three samples at each of the four dose levels) with 16,998 genes.
用信息论选择方法对剂量-反应微阵列实验趋势进行分类
剂量-反应微阵列实验包括监测数千个基因的表达水平,与所研究的治疗剂量增加有关。该实验的首要目标是建立剂量-反应关系,次要目标是确定最小有效剂量水平和确定剂量-反应曲线形状。最近,Lin等人(1)讨论了几种基于观测均值等压回归的单调趋势检验方法(2,3)。一旦建立了基因表达与剂量之间的单调关系,就有一组R个可能的单调模型可以拟合数据。从这组模型中选择最佳模型使我们能够确定剂量-反应曲线的形状和最小有效剂量水平。本文重点研究了利用信息论模型选择方法对剂量-反应曲线形状进行分类。特别地,讨论了订单限制信息准则(Order Restricted Information Criterion, ORIC)在订单限制下的推理。模型的后验概率是使用信息准则计算的,该信息准则考虑了模型的拟合优度和复杂性。该方法应用于一个剂量-反应微阵列实验,该实验有12个阵列(在4个剂量水平中每个有3个样本),包含16,998个基因。
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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