RAMPAGE
RAMPAGE profiles genome-wide polymerase III-transcribed Alu elements and integrates matching RNA-seq and epigenomic datasets to identify, quantify, and characterize their expression and potential regulatory roles.
Key Features:
- High-Resolution Data Generation: Generates high-resolution, long-span RAMPAGE genomic data across multiple biosamples to capture polymerase III transcription at Alu elements.
- Integration with RNA-seq Data: Incorporates matching RNA sequencing (RNA-seq) data from 155 biosamples to improve identification and quantification of expressed Alu elements.
- Comprehensive Atlas Creation: Builds an atlas comprising 17,249 polymerase III-transcribed Alu elements to map expression patterns across cell types.
- Multifaceted Integrative Analysis: Integrates ChIP-seq data for ten histone marks, ChIP-seq for hundreds of transcription factors, whole-genome bisulfite sequencing (WGBS) data, ChIA-PET data, and other functional genomic datasets across multiple biosamples.
- Cell-Type-Specific Enhancer Function Identification: Identifies that older, expressed Alu elements can act as cell-type-specific enhancers for nearby protein-coding genes while human-specific Alu elements remain transcriptionally repressed.
Scientific Applications:
- Expression Profiling: Identification and quantification of polymerase III-transcribed Alu elements across diverse biosamples.
- Regulatory Element Discovery: Detection of Alu-derived sequences that function as cell-type-specific enhancers for nearby protein-coding genes.
- Epigenomic Contextualization: Correlation of Alu transcription with histone modification patterns, transcription factor binding, DNA methylation (WGBS), and chromatin interactions (ChIA-PET).
- Repetitive Element-Gene Interaction Studies: Elucidation of interactions between repetitive Alu elements and gene expression regulation across different cell types.
Methodology:
Uses a pipeline to identify expressed Alu elements from high-resolution RAMPAGE data coupled with matching RNA-seq, and integrates diverse epigenomic datasets for contextual analysis.
Topics
Details
- License:
- MIT
- Programming Languages:
- Python
- Added:
- 11/14/2019
- Last Updated:
- 12/11/2020
Operations
Publications
Zhang X, Gingeras TR, Weng Z. Genome-wide analysis of polymerase III–transcribed <i>Alu</i> elements suggests cell-type–specific enhancer function. Genome Research. 2019;29(9):1402-1414. doi:10.1101/gr.249789.119. PMID:31413151. PMCID:PMC6724667.
PMID: 31413151
PMCID: PMC6724667
Funding: - National Institutes of Health: U24-HG009446
- NIH: U54-HG004557