HPeak
HPeak identifies genomic regions enriched in Chromatin Immunoprecipitation sequencing (ChIP-seq) data to map protein–DNA interactions using a Hidden Markov Model-based peak-finding algorithm.
Key Features:
- Hidden Markov Model (HMM) peak-finding: HPeak employs an HMM-based algorithm for peak detection in ChIP-seq data.
- Model-based statistical inference: The method assumes probability distributions to perform rigorous, model-based inference of enriched genomic regions.
- Novel weighting scheme: HPeak applies a weighting scheme to sequencing read coverage to improve accuracy in inferring enrichment.
- Motif enrichment validation: Evaluations reported a higher prevalence of expected transcription factor binding motifs in HPeak-enriched sequences versus controls.
- Improved resolution versus ChIP-chip: By leveraging ChIP-seq data, HPeak achieves higher resolution along with enhanced sensitivity and specificity relative to ChIP-chip for binding site detection.
Scientific Applications:
- Protein–DNA interaction mapping: Identification of genomic binding sites for transcription factors and other chromatin-associated proteins from ChIP-seq data.
- Cistroms surveys: Directly surveying the cistroms of transcription factors and chromatin-associated proteins.
- Regulatory network analysis: Supporting studies of genetic regulation and the regulatory networks that govern gene expression.
Methodology:
HPeak applies a Hidden Markov Model for peak finding, uses a novel weighting scheme on sequencing read coverage, and conducts model-based statistical inference by assuming probability distributions to identify enriched genomic regions.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- C++, Perl, Python
- Added:
- 1/13/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Qin ZS, Yu J, Shen J, Maher CA, Hu M, Kalyana-Sundaram S, Yu J, Chinnaiyan AM. HPeak: an HMM-based algorithm for defining read-enriched regions in ChIP-Seq data. BMC Bioinformatics. 2010;11(1). doi:10.1186/1471-2105-11-369. PMID:20598134. PMCID:PMC2912305.