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首页> 外文期刊>EURASIP journal on bioinformatics and systems biology >Using Temporal Correlation in Factor Analysis for Reconstructing Transcription Factor Activities
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Using Temporal Correlation in Factor Analysis for Reconstructing Transcription Factor Activities

机译:使用时间相关性在因子分析中重建转录因子活性

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摘要

Two-level gene regulatory networks consist of the transcription factors (TFs) in the top level and their regulated genes in the second level. The expression profiles of the regulated genes are the observed high-throughput data given by experiments such as microarrays. The activity profiles of the TFs are treated as hidden variables as well as the connectivity matrix that indicates the regulatory relationships of TFs with their regulated genes. Factor analysis (FA) as well as other methods, such as the network component algorithm, has been suggested for reconstructing gene regulatory networks and also for predicting TF activities. They have been applied to E. coli and yeast data with the assumption that these datasets consist of identical and independently distributed samples. Thus, the main drawback of these algorithms is that they ignore any time correlation existing within the TF profiles. In this paper, we extend previously studied FA algorithms to include time correlation within the transcription factors. At the same time, we consider connectivity matrices that are sparse in order to capture the existing sparsity present in gene regulatory networks. The TFs activity profiles obtained by this approach are significantly smoother than profiles from previous FA algorithms. The periodicities in profiles from yeast expression data become prominent in our reconstruction. Moreover, the strength of the correlation between time points is estimated and can be used to assess the suitability of the experimental time interval.
机译:二级基因调控网络由顶层的转录因子(TFs)和二级的调控基因组成。调控基因的表达谱是通过实验例如微阵列观察到的高通量数据。 TF的活性谱被视为隐藏变量以及连通性矩阵,该矩阵指示了TF及其调控基因的调控关系。已建议使用因子分析(FA)以及其他方法(例如网络组件算法)来重建基因调控网络并预测TF活性。假设这些数据集由相同且独立分布的样本组成,则已将它们应用于大肠杆菌和酵母数据。因此,这些算法的主要缺点是它们忽略了TF配置文件中存在的任何时间相关性。在本文中,我们扩展了先前研究的FA算法,以将时间相关性纳入转录因子中。同时,我们考虑了稀疏的连通性矩阵,以捕获基因调控网络中现有的稀疏性。通过这种方法获得的TFs活动概况比以前的FA算法的概况要平滑得多。来自酵母表达数据的概况的周期性在我们的重建中变得突出。此外,可以估计时间点之间的相关强度,并可将其用于评估实验时间间隔的适用性。

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