GreyListChIP

GreyListChIP identifies high-signal regions in ChIP-seq input control samples and filters reads mapping to those regions to reduce spurious peaks during peak calling and improve ChIP-seq data quality.


Key Features:

  • Identification of High-Signal Regions: Detects genomic regions with elevated signal in input control samples (input DNA) that can give rise to spurious peaks in ChIP-seq analyses.
  • Read Filtering Prior to Peak Calling: Removes reads aligning to identified high-signal regions before peak calling to reduce false-positive peaks.
  • Integration with Bioconductor: Implemented as a Bioconductor package in R to interoperate with other Bioconductor packages for downstream genomic analysis.

Scientific Applications:

  • Improved Peak Calling Accuracy: Reduces false-positive peak calls to aid in the identification of true protein-DNA interactions from ChIP-seq data.
  • Enhanced Data Quality in Genomic Studies: Produces cleaner ChIP-seq datasets that improve the reliability of downstream genomic analyses.
  • Integrative Genomic Workflows: Enables preprocessing of ChIP-seq data that can be integrated with other Bioconductor-based genomic workflows.

Methodology:

Operates in the R programming environment, analyzes input control samples to detect regions with disproportionately high signal, filters out reads mapping to those regions prior to peak calling, and integrates with other Bioconductor packages.

Topics

Collections

Details

License:
Artistic-2.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Publications

Huber W, Carey VJ, Gentleman R, Anders S, Carlson M, Carvalho BS, Bravo HC, Davis S, Gatto L, Girke T, Gottardo R, Hahne F, Hansen KD, Irizarry RA, Lawrence M, Love MI, MacDonald J, Obenchain V, Oleś AK, Pagès H, Reyes A, Shannon P, Smyth GK, Tenenbaum D, Waldron L, Morgan M. Orchestrating high-throughput genomic analysis with Bioconductor. Nature Methods. 2015;12(2):115-121. doi:10.1038/nmeth.3252. PMID:25633503. PMCID:PMC4509590.

Documentation

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