How it works
ATAC-seq uses Tn5 transposase to fragment accessible chromatin and insert sequencing adapters, producing a genome-wide map of open regions. Comparing cells, tissues or treatments can reveal changes in accessibility; integration with RNA-seq and ChIP-seq helps connect these changes to gene regulation.
Applications
- Compare accessible chromatin between treatment and control groups
- Identify regulatory regions for follow-up and analyze enriched motifs
- Relate accessibility changes to gene expression and develop regulatory hypotheses
Key features
- A streamlined workflow, with low-input options assessed for the sample type
- Genome-wide profiling of chromatin accessibility
- Supports integration with transcriptomic and protein-DNA interaction data
Workflow
- 01
Prepare cells or nuclei and assess sample quality
- 02
Perform Tn5 tagmentation to insert sequencing adapters
- 03
Amplify, assess and sequence libraries
- 04
Identify accessible regions and analyze differential accessibility and regulatory features
We tailor the experimental workflow and analysis to your samples and study objectives.