peakcalling_findpeaks

peakcalling_findpeaks identifies enriched genomic regions and transcription factor binding sites from ChIP-Seq aligned-read files to support genome-wide analysis of protein–DNA interactions.


Key Features:

  • Identification of Enrichment Areas: Identifies regions of gene enrichment and transcription factor binding sites within ChIP-Seq data.
  • Estimation of DNA Fragment Size Distributions: Estimates DNA fragment size distributions in enriched areas.
  • Generation of UCSC-Compatible WIG Track Files: Generates WIG track files compatible with the UCSC Genome Browser from aligned-read files produced by short-read sequencing technologies.
  • Platform Independence: Runs on any platform that supports a Java Runtime Environment.
  • Scalability and Resource Requirements: Memory usage scales with the number of sequencing reads, with approximately 4 GB of memory sufficient for processing up to 40 million reads.

Scientific Applications:

  • Regulatory Element Identification: Enables genome-wide identification of regulatory elements through detection of enriched regions in ChIP-Seq data.
  • Transcription Factor Binding Analysis: Supports mapping of transcription factor binding sites to study protein–DNA interactions.
  • Epigenetic and Gene Regulation Studies: Facilitates analysis of chromatin-associated signals relevant to epigenetic modifications and gene regulation.

Methodology:

Processes aligned-read files from short-read sequencing, identifies regions of enrichment and transcription factor binding sites, estimates DNA fragment size distributions in enriched areas, and outputs UCSC-compatible WIG track files.

Topics

Collections

Details

Maturity:
Mature
Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
12/19/2016
Last Updated:
11/25/2024

Operations

Data Inputs & Outputs

Publications

Afgan E, Baker D, van den Beek M, Blankenberg D, Bouvier D, Čech M, Chilton J, Clements D, Coraor N, Eberhard C, Grüning B, Guerler A, Hillman-Jackson J, Von Kuster G, Rasche E, Soranzo N, Turaga N, Taylor J, Nekrutenko A, Goecks J. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. Nucleic Acids Research. 2016;44(W1):W3-W10. doi:10.1093/nar/gkw343. PMID:27137889. PMCID:PMC4987906.

Mareuil F, Doppelt-Azeroual O, Ménager H. A public Galaxy platform at Pasteur used as an execution engine for web services. Unknown Journal. 2017. doi:10.7490/f1000research.1114334.1.

Fejes AP, Robertson G, Bilenky M, Varhol R, Bainbridge M, Jones SJM. FindPeaks 3.1: a tool for identifying areas of enrichment from massively parallel short-read sequencing technology. Bioinformatics. 2008;24(15):1729-1730. doi:10.1093/bioinformatics/btn305. PMID:18599518. PMCID:PMC2638869.

Links