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Computational prediction of transcription factor binding sites based on an integrative approach incorporating genomic and epigenomic features

机译:基于整合了基因组和表观基因组特征的整合方法的转录因子结合位点的计算预测

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Transcription factor binding sites (TFBSs) are often predicted by sequence-based methods that use a position weight matrix or consensus sequences. However, the degeneracy of TFBSs makes the prediction of them very challenging. Recent completion of the encyclopedia of DNA elements project provides many useful additional information enabling researchers to tackle these difficulties from a noble point of view. In this paper we developed an integrative TFBS prediction method incorporating genomic as well as epigenomic features, such as DNA methylation, histone modification and chromatin accessibility. We found that (i) an integration of various features facilitates more accurate TFBS prediction, (ii) the proximity range of -500 to 500 nt relative to the transcription start site of a gene resulted in slightly more accurate prediction than the other ranges, and (iii) the proximity of an epigenomic feature contributes more than the other properties of epigenomic or genomic features to the accurate prediction of TFBSs. This study demonstrates that epigenomic features play a critical role in an integrative approach for predicting TFBSs.
机译:转录因子结合位点(TFBS)通常是通过使用位置权重矩阵或共有序列的基于序列的方法预测的。但是,TFBS的简并性使其预测非常具有挑战性。 DNA元素百科全书项目的最新完成提供了许多有用的附加信息,使研究人员可以从高尚的角度解决这些困难。在本文中,我们开发了一种集成的TFBS预测方法,该方法结合了基因组和表观基因组特征,例如DNA甲基化,组蛋白修饰和染色质可及性。我们发现(i)各种功能的整合有助于更准确的TFBS预测,(ii)相对于基因转录起始位点的-500到500 nt的邻近范围导致比其他范围的预测更加准确,并且(iii)表观基因组特征的邻近性比表观基因组或基因组特征的其他特性对TFBS的准确预测贡献更大。这项研究表明,表观基因组特征在预测TFBS的综合方法中起着至关重要的作用。

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