• Media type: E-Article
  • Title: NoPeak: k-mer-based motif discovery in ChIP-Seq data without peak calling
  • Contributor: Menzel, Michael; Hurka, Sabine; Glasenhardt, Stefan; Gogol-Döring, Andreas
  • imprint: Oxford University Press (OUP), 2021
  • Published in: Bioinformatics
  • Language: English
  • DOI: 10.1093/bioinformatics/btaa845
  • ISSN: 1367-4803; 1367-4811
  • Keywords: Computational Mathematics ; Computational Theory and Mathematics ; Computer Science Applications ; Molecular Biology ; Biochemistry ; Statistics and Probability
  • Origination:
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  • Description: <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Motivation</jats:title> <jats:p>The discovery of sequence motifs mediating DNA-protein binding usually implies the determination of binding sites using high-throughput sequencing and peak calling. The determination of peaks, however, depends strongly on data quality and is susceptible to noise.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Here, we present a novel approach to reliably identify transcription factor-binding motifs from ChIP-Seq data without peak detection. By evaluating the distributions of sequencing reads around the different k-mers in the genome, we are able to identify binding motifs in ChIP-Seq data that yield no results in traditional pipelines.</jats:p> </jats:sec> <jats:sec> <jats:title>Availability and implementation</jats:title> <jats:p>NoPeak is published under the GNU General Public License and available as a standalone console-based Java application at https://github.com/menzel/nopeak.</jats:p> </jats:sec> <jats:sec> <jats:title>Supplementary information</jats:title> <jats:p>Supplementary data are available at Bioinformatics online.</jats:p> </jats:sec>
  • Access State: Open Access