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 3-D genome architectural signals while preserving all the applications and capabilities of whole genome shotgun sequencing data.
A short 3-minute video on a multi-application approach to Library Prep:
Accompanying 6-page Slide Deck:
Omni-C Sample Prep offers genome-wide coverage that is:
- Free of restriction enzyme density bias
- Sample inputs down to 1000 cells
- Compatible with hybrid capture approaches