rGADEM
rGADEM performs de novo motif discovery and analysis on ChIP-Seq and large-scale genomic sequence datasets to identify co-occurring motifs associated with transcription factor binding.
Key Features:
- Integrated Analysis Pipeline: An R-based pipeline covering data input, peak detection, sequence and motif analysis, visualization, and data export.
- GADEM foundation: Extends the GADEM de novo motif discovery algorithm.
- R implementation: Implemented as an R package for integration with R and Bioconductor workflows.
- Scalability and Performance: Scales to tens of thousands of enriched regions and is optimized for multicore computers.
- Motif Discovery and Analysis: Performs de novo motif discovery and identifies co-occurring motifs with sensitivity to detect motifs aligned with the literature.
- Extensibility: Extensible through incorporation of additional R and Bioconductor packages.
- Visualization and Data Export: Produces sequence and motif visualizations and supports comprehensive data export.
Scientific Applications:
- ChIP-Seq motif discovery: Identification of transcription factor binding motifs from ChIP-Seq datasets and analysis of enriched genomic regions.
- Human transcription factor studies: Demonstrated on human ChIP-Seq datasets for FOXA1, ER, CTCF, and STAT1, recovering motifs consistent with published literature and detecting motifs missed by other methods.
Methodology:
Input of genomic sequence data, peak detection to identify regions of enrichment, sequence and motif analysis for de novo motif discovery and co-occurring motif identification, and generation of visualizations with data export.
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
Mercier E, Droit A, Li L, Robertson G, Zhang X, Gottardo R. An Integrated Pipeline for the Genome-Wide Analysis of Transcription Factor Binding Sites from ChIP-Seq. PLoS ONE. 2011;6(2):e16432. doi:10.1371/journal.pone.0016432. PMID:21358819. PMCID:PMC3040171.