ATAC-seq
Recommended Analysis Workflow
Primary Recommendation: nf-core/atacseq + atacreportR
For ATAC-seq projects, we recommend using nf-core/atacseq for initial processing followed by our atacreportR application for differential accessibility analysis and comprehensive reporting.
Workflow Overview:
- Raw data processing → Run nf-core/atacseq on HiperGator using SLURM configuration
- Differential analysis & reporting → Use atacreportR to generate comprehensive differential accessibility reports
- Interactive exploration → Review results through atacreportR’s downloadable reports
Important Access Notes:
- atacreportR is a private application accessible only on the UF network
- Contact our team for access to the required HiperGator data location to run the application
- VPN connection required for off-campus access
Alternative R-based Analysis
For users preferring traditional R workflows, we recommend:
- DiffBind for differential binding analysis
- ChIPseeker for peak annotation
- Access via RStudio Server on HiperGator
Best Practices & Considerations
Experimental Design:
- Plan for adequate biological replicates (minimum 3 per condition)
- Include appropriate input/background controls
- Consider cell type purity and sample quality
Data Quality:
- Evaluate fragment size distribution and TSS enrichment from nf-core/atacseq output
- Check for proper peak calling and reproducibility between replicates
- Assess library complexity and duplication rates
Analysis Strategy:
- Define appropriate peak calling parameters for your cell type
- Consider motif enrichment analysis for biological interpretation
- Plan integration with RNA-seq data when available
Computational Resources:
- Use HiperGator’s SLURM scheduler for nf-core/atacseq processing
- Allocate sufficient memory for peak calling (depends on genome size)
- Plan storage for large BAM files and peak call outputs
Getting Started
Submit a support request to discuss your ATAC-seq project design, analysis needs, and to obtain access to atacreportR.