An order estimation based approach to identify response genes for microarray time course data.

IF 0.8 4区 数学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Statistical Applications in Genetics and Molecular Biology Pub Date : 2012-12-14 DOI:10.1515/1544-6115.1818
Zhiheng K Lu, O Brian Allen, Anthony F Desmond
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引用次数: 2

Abstract

Gene expression profiles from microarray time course experiments provide a unique opportunity to examine genome-wide signal processing and gene responses. A fundamental issue in microarray experiments is that the treatment condition can only be controlled at the cell level rather than at the gene level. The treatment condition does not affect all genes equally. Some genes depend on other genes to detect external changes. The dependency between genes is not fully deterministic and may vary with treatment condition. Thus the expression of each gene is potentially affected by two confounding effects: the treatment effect and the gene context effect arising from the regulatory interactions among genes. This gene context effect is hard to isolate. Neither can it be simply ignored. Instead, this gene context information which may be different under different treatment conditions is of primary biological interest. We introduce an approach which deals with the confounding effects and takes into account the uncontrollable gene context effect. Our method is based on the estimation of the number of hidden states, which, in our development, corresponds to the order of a hidden Markov model (HMM). For each gene, its observed expression is modeled by a gamma distribution determined by the corresponding hidden state at each time point. Those genes showing evidence for more than one hidden state can be categorized as the signalling genes, or in a wider sense, as the response genes which are coordinated by a cell system in reaction to a specific external condition. These response genes can be used in the comparison of different treatment conditions, to investigate the gene context effect under different treatments. Microarray time course data are also analyzed to demonstrate our method.

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基于序估计的微阵列时间过程数据响应基因识别方法。
基因表达谱从微阵列时间过程实验提供了一个独特的机会来检查全基因组的信号处理和基因反应。微阵列实验的一个基本问题是,治疗条件只能在细胞水平而不是在基因水平上进行控制。治疗条件对所有基因的影响并不相同。一些基因依赖其他基因来检测外部变化。基因之间的依赖性不是完全确定的,可能随治疗条件而变化。因此,每个基因的表达都可能受到两种混杂效应的影响:治疗效应和基因间调节相互作用产生的基因背景效应。这种基因背景效应很难分离出来。也不能简单地忽略它。相反,这种基因背景信息在不同的处理条件下可能会有所不同,这是主要的生物学兴趣。我们介绍了一种处理混杂效应并考虑不可控基因环境效应的方法。我们的方法是基于隐状态数的估计,在我们的开发中,隐状态数对应于隐马尔可夫模型(HMM)的阶数。对于每个基因,其观察到的表达由每个时间点对应的隐藏状态确定的gamma分布来建模。那些显示出不止一种隐藏状态证据的基因可以被归类为信号基因,或者在更广泛的意义上,作为响应基因,由细胞系统对特定外部条件的反应进行协调。这些应答基因可用于不同处理条件的比较,探讨不同处理条件下的基因环境效应。微阵列时间过程数据也进行了分析,以证明我们的方法。
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来源期刊
Statistical Applications in Genetics and Molecular Biology
Statistical Applications in Genetics and Molecular Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-MATHEMATICAL & COMPUTATIONAL BIOLOGY
自引率
11.10%
发文量
8
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
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