Principle
RRBS enriches CpG-rich regions through restriction digestion and fragment selection, followed by bisulfite treatment, amplification and sequencing. It focuses methylation comparisons on covered promoters, CpG islands and other selected regions.
Applications
- Study methylation during differentiation and development
- Compare CpG-rich regions associated with disease or treatment
- Assess drug-related methylation changes within covered regions
Method features
- Single-base resolution within the achieved coverage
- Focuses data on CpG-rich regions
- Project design considers sites jointly covered across samples
Workflow
- 01
Extract and digest DNA
- 02
Select fragments and perform bisulfite conversion
- 03
Amplify, assess and sequence libraries
- 04
Quantify and compare methylation within covered regions
This is a workflow overview. Experimental and analytical details depend on sample conditions and research objectives.