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Hidden Markov Models for Microarray Time Course Data in Multiple Biological Conditions

机译:多种生物条件下微阵列时程数据的隐马尔可夫模型

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Among the first microarray experiments were those measuring expression over time, and time course experiments remain common. Most methods to analyze time course data attempt to group genes sharing similar temporal profiles within a single biological condition. However, with time course data in multiple conditions, a main goal is to identify differential expression patterns over time. An intuitive approach to this problem would be to apply at each time point any of the many methods for identifying differentially expressed genes across biological conditions and then somehow combine the results of the repeated marginal analyses. But considering each time point in isolation is inefficient, because it does not use the information contained in the dependence structure of the time course data. This problem is exacerbated in microarray studies, where low sensitivity is a problematic feature of many methods. Furthermore, a gene's expression pattern over time might not be identified by simply combining results from repeated marginal analyses. We propose a hidden Markov modeling approach developed to efficiently identify differentially expressed genes in time course microarray experiments and classify genes based on their temporal expression patterns. Simulation studies demonstrate a substantial increase in sensitivity, with little increase in the false discovery rate, compared with a marginal analysis at each time point. This increase is also observed in data from a case study of the effects of aging on stress response in heart tissue, where a significantly larger number of genes are identified using the proposed approach.
机译:在最初的微阵列实验中,有一些是随时间测量表达的,而时程实验仍然很普遍。分析时程数据的大多数方法都试图对在单个生物学条件下共享相似时间分布的基因进行分组。但是,对于处于多个条件下的时程数据,主要目标是随着时间的推移识别差异表达模式。解决此问题的一种直观方法是在每个时间点应用多种方法来鉴定跨生物学条件的差异表达基因,然后以某种方式组合重复的边际分析结果。但是孤立地考虑每个时间点是无效的,因为它不使用时程数据的依存结构中包含的信息。在微阵列研究中,这个问题更加严重,因为低灵敏度是许多方法的一个有问题的特征。此外,可能无法通过简单地组合重复的边际分析结果来确定基因随时间的表达模式。我们提出了一种隐马尔可夫建模方法,以在时程微阵列实验中有效识别差异表达的基因并根据其时间表达模式对基因进行分类。仿真研究表明,与每个时间点的边际分析相比,灵敏度显着提高,而错误发现率几乎没有提高。在衰老对心脏组织中的应激反应的影响的案例研究中的数据中也观察到了这种增加,其中使用提议的方法鉴定出明显更多的基因。

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