Tian Tianhai
Monash University, Melbourne, Vic, Australia.
Biosystems. 2010 Mar;99(3):192-200. doi: 10.1016/j.biosystems.2009.11.002. Epub 2009 Nov 27.
Microarray expression profiles are inherently noisy and many different sources of variation exist in microarray experiments. It is still a significant challenge to develop stochastic models to realize noise in microarray expression profiles, which has profound influence on the reverse engineering of genetic regulation. Using the target genes of the tumour suppressor gene p53 as the test problem, we developed stochastic differential equation models and established the relationship between the noise strength of stochastic models and parameters of an error model for describing the distribution of the microarray measurements. Numerical results indicate that the simulated variance from stochastic models with a stochastic degradation process can be represented by a monomial in terms of the hybridization intensity and the order of the monomial depends on the type of stochastic process. The developed stochastic models with multiple stochastic processes generated simulations whose variance is consistent with the prediction of the error model. This work also established a general method to develop stochastic models from experimental information.
微阵列表达谱本质上是有噪声的,并且在微阵列实验中存在许多不同的变异来源。开发随机模型以实现微阵列表达谱中的噪声仍然是一项重大挑战,这对基因调控的逆向工程有深远影响。以肿瘤抑制基因p53的靶基因作为测试问题,我们开发了随机微分方程模型,并建立了随机模型的噪声强度与用于描述微阵列测量分布的误差模型参数之间的关系。数值结果表明,具有随机降解过程的随机模型的模拟方差可以用杂交强度的单项式表示,单项式的阶数取决于随机过程的类型。具有多个随机过程的已开发随机模型生成的模拟结果,其方差与误差模型的预测一致。这项工作还建立了一种从实验信息开发随机模型的通用方法。