SICER
SICER identifies broad domains of enrichment from histone modification ChIP-Seq data to map chromatin states relevant to gene regulation and cell identity.
Key Features:
- Domain Identification: Identifies broad domains of histone modification enrichment from ChIP-Seq data rather than focusing on localized peaks.
- Signal Clustering: Employs clustering of signals across neighboring nucleosomes to detect groups of enrichment that are unlikely to occur by chance, pooling adjacent nucleosome information to enhance detection.
- Genomic-Scale Analysis: Performs genome-scale analyses to map epigenetic states across entire genomes.
- Validation and Performance: Validated on loci with known epigenetic states and demonstrates superior sensitivity and specificity for histone modification profiles compared to existing methods.
- Data Normalization: Provides an unbiased approach applicable to data normalization for quantitative comparisons of epigenetic modifications across cell types and growth conditions.
Scientific Applications:
- Epigenetic Research: Enables exploration of chromatin states and their roles in gene regulation by identifying enriched histone modification domains.
- Comparative Genomics: Supports comparative studies of epigenetic landscapes across species at genomic scale.
- Functional Genomics: Facilitates investigation of how epigenetic modifications influence cellular processes and identity.
Methodology:
Aggregates ChIP-Seq signal enrichment across neighboring nucleosomes and uses spatial clustering to identify contiguous domains of histone modification enrichment that are statistically unlikely by chance.
Topics
Details
- Maturity:
- Mature
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- Python
- Added:
- 1/13/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Zang C, Schones DE, Zeng C, Cui K, Zhao K, Peng W. A clustering approach for identification of enriched domains from histone modification ChIP-Seq data. Bioinformatics. 2009;25(15):1952-1958. doi:10.1093/bioinformatics/btp340. PMID:19505939. PMCID:PMC2732366.