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.

Documentation