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MotEvo: integrated Bayesian probabilistic methods for inferring regulatory sites and motifs on multiple alignments of DNA sequences

机译:MotEvo:综合贝叶斯概率方法,用于推断DNA序列多重比对中的调控位点和基序

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摘要

Motivation: Probabilistic approaches for inferring transcription factor binding sites (TFBSs) and regulatory motifs from DNA sequences have been developed for over two decades. Previous work has shown that prediction accuracy can be significantly improved by incorporating features such as the competition of multiple transcription factors (TFs) for binding to nearby sites, the tendency of TFBSs for co-regulated TFs to cluster and form cis-regulatory modules and explicit evolutionary modeling of conservation of TFBSs across orthologous sequences. However, currently available tools only incorporate some of these features, and significant methodological hurdles hampered their synthesis into a single consistent probabilistic framework. Results: We present MotEvo, a integrated suite of Bayesian probabilistic methods for the prediction of TFBSs and inference of regulatory motifs from multiple alignments of phylogenetically related DNA sequences, which incorporates all features just mentioned. In addition, MotEvo incorporates a novel model for detecting unknown functional elements that are under evolutionary constraint, and a new robust model for treating gain and loss of TFBSs along a phylogeny. Rigorous benchmarking tests on ChIP-seq datasets show that MotEvo's novel features significantly improve the accuracy of TFBS prediction, motif inference and enhancer prediction. Availability: Source code, a user manual and files with several example applications are available at www.swissregulon.unibas.ch. Contact: erik.vannimwegen@unibas.ch Supplementary information: Supplementary data are available at Bioinformatics online
机译:动机:从DNA序列推断转录因子结合位点(TFBS)和调控基序的概率方法已经开发了二十多年。先前的工作表明,通过合并多个转录因子(TF)竞争与附近位点的结合,TFBS共同调控的TF聚集并形成顺式调控模块和显性的特征,可以显着提高预测准确性。跨同源序列的TFBS保守性的进化模型。但是,当前可用的工具仅包含这些功能中的一些功能,并且重大的方法障碍阻碍了它们的综合到一个一致的概率框架中。结果:我们提出了MotEvo,这是一种贝叶斯概率方法的集成套件,可用于从系统发育相关的DNA序列的多次比对中预测TFBS并推断调控基序,其中包括了刚才提到的所有功能。此外,MotEvo包含用于检测处于进化约束下的未知功能元件的新型模型,以及用于处理沿系统发育的TFBS的获得和丧失的新的稳健模型。对ChIP-seq数据集的严格基准测试表明,MotEvo的新颖功能显着提高了TFBS预测,基序推断和增强子预测的准确性。可用性:可从www.swissregulon.unibas.ch获得源代码,用户手册以及带有几个示例应用程序的文件。联系人:erik.vannimwegen@unibas.ch补充信息:补充数据可在在线生物信息学中获得

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