Van Belle Werner, Gerits Nancy, Jakobsen Kirsti, Brox Vigdis, Van Ghelue Marijke, Moens Ugo
Department of Microbiology and Virology, Section Virology, Faculty of Medicine, University of Tromsø, Norway.
Gene Regul Syst Bio. 2007 Jul 17;1:57-72.
To perform a quantitative analysis with gene-arrays, one must take into account inaccuracies (experimental variations, biological variations and other measurement errors) which are seldom known. In this paper we investigated amplification and noise propagation related errors by measuring intensity dependent variations. Based on a set of control samples, we create confidence intervals for up and down regulations. We validated our method through a qPCR experiment and compared it to standard analysis methods (including loess normalization and filtering methods based on genetic variability). The results reveal that amplification related errors are a major concern.
要使用基因芯片进行定量分析,必须考虑到那些鲜为人知的不准确性(实验变异、生物变异及其他测量误差)。在本文中,我们通过测量强度依赖性变异来研究与扩增及噪声传播相关的误差。基于一组对照样本,我们为上调和下调创建了置信区间。我们通过定量聚合酶链反应实验验证了我们的方法,并将其与标准分析方法(包括局部加权回归归一化和基于基因变异性的过滤方法)进行了比较。结果表明,与扩增相关的误差是一个主要问题。