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.