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Application of Kernel Method to Reveal Subtypes of TF Binding Motifs Causal Analysis of Gene Expression Data

机译:核法揭示TF结合基序亚型基因表达数据的亚型

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Transcription factor binding sites often contain several subtypes of sequences that follow not just one but several different patterns. We developed a novel sensitive method based on kernel estimations that is able to reveal subtypes of TF binding sites. The developed method produces patterns in form of positional weight matrices for the individual subtypes and has been tested on simulated data and compared with several other methods of pattern discovery (Gibbs sampling, MEME, CONSENSUS, MULTTPROFTLER and PROJECTION). The kernel method showed the best performance in terms of how close the revealed weight matrices are to the original ones. We applied the Kernel method to several TFs including nuclear receptors and ligand-activated transcription factors AhR. The revealed patterns were applied to analyze gene expression data. In promoters of differentially expressed genes we found specific combinations of different types of TF binding patterns that correlate with the level of up or down regulation.
机译:转录因子结合位点通常含有几个序列亚型,其不仅仅是一种但几种不同的模式。我们开发了一种基于内核估计的新型敏感方法,能够揭示TF结合站点的亚型。开发方法以各个亚型的位置重量矩阵的形式产生图案,并且已经在模拟数据上测试并与其他几种模式发现方法(GIBBS采样,MEME,共识,多电板和投影相比。内核方法在揭示的权重矩阵对原始矩阵的接近方面表现出最佳性能。我们将内核方法应用于几种TFS,包括核受体和配体活化转录因子AHR。揭示的模式被应用于分析基因表达数据。在差异表达基因的启动子中,我们发现不同类型的TF结合模式的特定组合,其与上下调节的水平相关。

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