The biological genome is one of mankind’s most exciting and largely undiscovered frontiers. With NGS technologies and bioinformatics capabilities having delivered thousands of new genome sequences over the last two decades and adding more every day, the door to this complex and fascinating world has been cast wide open! Take a giant leap into the vast landscape of genotype and variant analysis with the Inscripta® Onyx platform, your most powerful tool in the next phase of Genome Discovery.
Uncovering novel phenotypes needs no longer to be tied to random mutagenesis approaches or simple knock-out libraries. The Onyx CRISPR-based benchtop digital genome engineering platform delivers a high-throughput and precise gene editing capability genome-wide to dramatically kickstart or massively accelerate your most important Genomic Discovery programs.
Take a deeper dive into the genes, pathways, and networks you care about most. Or probe the entire genome for something new and undiscovered. The Genome Discovery frontier is
yours to explore.
Learn more by browsing our sample applications below.
Complex phenotypes like tolerance often have complex genetic foundations. Interested in unearthing the genes underpinning cellular behavior? Learn how genome-wide libraries were used to probe osmotic stress response in E. coli
Adaptive laboratory evolution (ALE) is a powerful genomic discovery approach. If you don’t mind the time commitment. What if you could compress your discovery and validation timelines dramatically?
Have you ever wanted to explore an interesting locus in its native genomic context? See how the Onyx technology was used to survey the entire mutational space of four essential E. coli genes to map functionality
Contact us to learn more about how your lab’s Genome Discovery efforts can benefit from the Onyx benchtop genome engineering platform and barcode analysis tools.
Want to learn more about the Onxy platform and what we’ve been up to? Check out our latest videos, webinars, and presentations and get answers to our FAQs on the Resource & Support page.
