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
Learn More about Omni-C™

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