ChIP-seq Analysis

Overview

Chromatin immunoprecipitation sequencing (ChIP-seq) is used to analyze protein interactions with DNA. It combines chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to identify the binding sites of DNA-associated proteins.

parse2wig

parse2wig is a tool for converting aligned read files to wiggle format, which is useful for visualization in genome browsers.

3. Peak Calling

Peak calling is a crucial step in ChIP-seq analysis, identifying regions of the genome where proteins of interest are bound. Several tools are available:

Tool Description Source
MACS2[^1] Model-based Analysis of ChIP-Seq. Captures local biases in sequencing data and models peak shape to improve accuracy. GitHub
IDR[^2] Irreproducible Discovery Rate. Assesses reproducibility of findings across replicates. GitHub
phantompeakqualtools[^3] A package for ChIP-seq quality control metrics, including strand cross-correlation. GitHub

4. Visualization and Analysis

DROMPA

DROMPA (DRaw and Observe Multiple enrichment Profiles and Annotation) is a comprehensive tool for easy-to-handle peak calling and visualization in ChIP-seq data analysis[^4].

Key features:

  • Peak calling
  • Visualization of enrichment profiles
  • Annotation of peaks
  • Computational analysis and validation of ChIP-seq data
Feature Description
Peak Calling Identifies significant binding sites using a sliding window approach
Visualization Generates publication-quality figures of ChIP-seq enrichment profiles
Annotation Associates peaks with genomic features (e.g., promoters, genes)
Comparative Analysis Allows comparison of multiple ChIP-seq datasets

References

[^1]: Zhang Y, Liu T, Meyer CA, et al. Model-based Analysis of ChIP-Seq (MACS). Genome Biol. 2008;9(9):R137. PMID: 18798982

[^2]: Li Q, Brown JB, Huang H, Bickel PJ. Measuring reproducibility of high-throughput experiments. Ann Appl Stat. 2011;5(3):1752-1779. DOI: 10.1214/11-AOAS466

[^3]: Landt SG, Marinov GK, Kundaje A, et al. ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. Genome Res. 2012;22(9):1813-1831. PMID: 22955991

[^4]: Nakato R, Itoh T, Shirahige K. DROMPA: easy-to-handle peak calling and visualization software for the computational analysis and validation of ChIP-seq data. Genes Cells. 2013;18(7):589-601. PMID: 23672187

Created by Ryan D. Najac for the Palomero Lab at the Institute for Cancer Genetics.
Page last updated on 2024-10-17.