Literature DB >> 22334039

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

Phil Arnold1, Ionas Erb, Mikhail Pachkov, Nacho Molina, Erik van Nimwegen.   

Abstract

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.

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Year:  2012        PMID: 22334039     DOI: 10.1093/bioinformatics/btr695

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  41 in total

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7.  oPOSSUM-3: advanced analysis of regulatory motif over-representation across genes or ChIP-Seq datasets.

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8.  Use of ChIP-Seq data for the design of a multiple promoter-alignment method.

Authors:  Ionas Erb; Juan R González-Vallinas; Giovanni Bussotti; Enrique Blanco; Eduardo Eyras; Cédric Notredame
Journal:  Nucleic Acids Res       Date:  2012-01-09       Impact factor: 16.971

9.  Skeletal muscle PGC-1α modulates systemic ketone body homeostasis and ameliorates diabetic hyperketonemia in mice.

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Journal:  FASEB J       Date:  2016-02-05       Impact factor: 5.191

10.  Transcriptional network analysis in muscle reveals AP-1 as a partner of PGC-1α in the regulation of the hypoxic gene program.

Authors:  Mario Baresic; Silvia Salatino; Barbara Kupr; Erik van Nimwegen; Christoph Handschin
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