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Computational inference of transcriptional regulatory networks from expression profiling and transcription factor binding site identification

机译:从表达谱和转录因子结合位点识别计算转录调控网络的计算推断

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We have developed a computational method for transcriptional regulatory network inference, CARRIE (Computational Ascertainment of Regu latory Relationships Inferred from Expression), which combines microarray and promoter sequence analysis. CARRIE uses sources of data to identify the transcription factors (TFs) that regulate gene expression changes in response to a stimulus and generates testable hypotheses about the regulatory network connecting these TFs to the genes they regulate. The promoter analysis component of CARRIE, ROVER (Relative OVER‐abundance of cis‐elements), is highly accurate at detecting the TFs that regulate the response to a stimulus. ROVER also predicts which genes are regulated by each of these TFs. CARRIE uses these transcriptional interactions to infer a regulatory network. To demonstrate our method, we applied CARRIE to six sets of publicly available DNA microarray experiments on Saccharomyces cerevisiae. The predicted networks were validated with comparisons to literature sources, experimental TF binding data, and gene ontology biological process information.
机译:我们已经开发了一种转录调控网络推论的计算方法,CARRIE(从表达推论的调节关系的计算确定),该方法结合了微阵列和启动子序列分析。 CARRIE利用数据源来识别转录因子(TF),这些因子可调节基因表达以响应刺激,并产生有关将这些TF与它们调控的基因相连的调控网络的可验证假设。 CARRIE的启动子分析组件ROVER(顺式元素相对过量)在检测调节对刺激反应的TF方面非常准确。 ROVER还可以预测每个TF调控哪些基因。 CARRIE使用这些转录相互作用来推断调控网络。为了证明我们的方法,我们将CARRIE应用于啤酒酵母的六组公开可用的DNA微阵列实验。通过与文献来源,实验性TF结合数据以及基因本体生物学过程信息的比较,验证了预测的网络。

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