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Stochastic models for inferring genetic regulation from microarray gene expression data

机译:从微阵列基因表达数据推断遗传调控的随机模型

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摘要

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.
机译:微阵列表达谱本质上是嘈杂的,并且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个重大挑战,这对基因调控的逆向工程产生了深远的影响。以抑癌基因p53的靶基因为测试问题,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值分布的误差模型的参数之间的关系。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,并且单项式的顺序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了模拟,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中开发随机模型的通用方法。

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