Jarrett Richard G, Ruggiero Katya
CSIRO Mathematical and Information Sciences, Private Bag 33, Clayton South 3169, Australia.
Biometrics. 2008 Mar;64(1):208-16. doi: 10.1111/j.1541-0420.2007.00835.x. Epub 2007 Jul 25.
Gene expression microarray experiments are intrinsically two-phase experiments. Messenger RNA (mRNA), required for the microarray experiment, must first be derived from plants or animals that are exposed to a set of treatments in a previous experiment (Phase 1). The mRNA is then used in the subsequent laboratory-based microarray experiment (Phase 2) from which gene expression is measured and ultimately analyzed. We show that obtaining a valid test for the effects of treatments on gene expression depends on the design of both the Phase 1 and Phase 2 experiments. Examples show that the multiple dye-swap design at Phase 2 is more robust than the alternating loop design in the absence of prior knowledge of the relative size of variation in the Phase 1 and Phase 2 experiments.
基因表达微阵列实验本质上是两阶段实验。微阵列实验所需的信使核糖核酸(mRNA)必须首先从先前实验(第一阶段)中接受一组处理的植物或动物中获取。然后,mRNA被用于后续基于实验室的微阵列实验(第二阶段),从中测量并最终分析基因表达。我们表明,要获得关于处理对基因表达影响的有效检验,取决于第一阶段和第二阶段实验的设计。实例表明,在对第一阶段和第二阶段实验变异相对大小缺乏先验知识的情况下,第二阶段的多重染料交换设计比交替循环设计更稳健。