The Omni-C™ Kit enables NGS library prep that supports multiple whole genome sequencing applications:
- Large structural variant detection
- SNP & InDel genotyping
- Perform genome assembly
- Perform haplotype phasing
- Capture chromatin conformation data
With a single library prep, you can capture epigenetic and 3D genome architectural signals while preserving all the applications and capabilities of whole genome shotgun sequencing data.