Zhao Changyong, Li Xiaoman, Hu Haiyan
Department of Electrical Engineering &Computer Science, University of Central Florida, Orlando, FL, 32816, USA.
Burnett School of Biomedical Science, University of Central Florida, Orlando, FL, 32816, USA.
Sci Rep. 2016 Jul 20;6:30043. doi: 10.1038/srep30043.
The identification of enhancer-target gene (ETG) pairs is vital for the understanding of gene transcriptional regulation. Experimental approaches such as Hi-C have generated valuable resources of ETG pairs. Several computational methods have also been developed to successfully predict ETG interactions. Despite these progresses, high-throughput experimental approaches are still costly and existing computational approaches are still suboptimal and not easy to apply. Here we developed a motif module based approach called PETModule that predicts ETG pairs. Tested on eight human cell types and two mouse cell types, we showed that a large number of our predictions were supported by Hi-C and/or ChIA-PET experiments. Compared with two recently developed approaches for ETG pair prediction, we shown that PETModule had a much better recall, a similar or better F1 score, and a larger area under the receiver operating characteristic curve. The PETModule tool is freely available at http://hulab.ucf.edu/research/projects/PETModule/.
增强子-靶基因(ETG)对的识别对于理解基因转录调控至关重要。诸如Hi-C等实验方法已产生了ETG对的宝贵资源。也已开发了几种计算方法来成功预测ETG相互作用。尽管取得了这些进展,但高通量实验方法仍然成本高昂,并且现有的计算方法仍然不够理想且不易应用。在此,我们开发了一种基于基序模块的方法,称为PETModule,用于预测ETG对。在八种人类细胞类型和两种小鼠细胞类型上进行测试后,我们表明我们的大量预测得到了Hi-C和/或ChIA-PET实验的支持。与最近开发的两种用于ETG对预测的方法相比,我们表明PETModule具有更好的召回率、相似或更好的F1分数以及更大的受试者工作特征曲线下面积。PETModule工具可在http://hulab.ucf.edu/research/projects/PETModule/免费获取。