Date/Time: March 5, 2019 • 9am PDT | 12pm EDT
Learn about VERG, a novel high-throughput cell platform for characterizing genes and proteins of interest. VERG enables organisations to rapidly understand the effects of coding variations on their genes/proteins of interest as it relates to biology, drug development and synthetic biology. Helping to power VERG is VariantFind™, a patent pending technology for building DNA variant libraries. VariantFind’s three-step (design, build and validate) workflow helps organizations build scanning and combinatorial libraries in a powerful and flexible manner.
The webinar features VERG experts from Ranomics, an innovative biotechnology company that helps organizations enable transformative discoveries using genomics.
Join this webinar to learn about:
- How exploiting genetic variations can help you build and engineer better life sciences products
- How to find genetic variations, for example, that are in proximity to exon-intron junctions, therefore having a high chance of perturbing gene function, and which could result in disease causation.
- How VERG technology can help you measure binding interactions across thousands of protein variants in a single workflow.
- …and more.
Presenter: Nikko Torres, Ph.D.
Research Scientist, Ranomics
Nikko Torres, Ph.D. is a research scientist at Ranomics, where he develops highly parallel cell-based functional assays and generates DNA variant libraries. Nikko is a cell biologist and data analyst with over a decade of experience in developing high-throughput methods to ask macro-level questions in microbiology.