NoPeak: k-mer-based motif discovery in ChIP-Seq data without peak calling.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32991679.
- Also identified by DOI 10.1093/bioinformatics/btaa845.
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Abstract
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. 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. NoPeak is published under the GNU General Public License and available as a standalone console-based Java application at https://github.com/menzel/nopeak. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Chromatin Immunoprecipitation Sequencing
- High-Throughput Nucleotide Sequencing