Advancing Structural Variant Analysis in Human Genomics, Cytogenetics, and Cell and Gene Therapy
Lunch and Learn
Reserve Your Spot!
Mark your calendars for June 18th, 2025 and join Nabsys at UCSD to explore electronic genome mapping (EGM), a cost-effective and accessible solution for structural variation (SV) analysis using electronic nanodetection technology. EGM makes high-resolution SV analysis available to everyone, empowering researchers to expand the boundaries of their genomics research. Its ability to provide detailed SV mapping and confirmation opens new possibilities in human genomics, cytogenetics, and cell and gene therapy. With accessibility, accuracy and scalability, EGM simplifies SV detection and will help drive your disease research and discovery forward.
Session Details:
Title: Advancing Structural Variant Analysis in Human Genomics, Cytogenetics, and Cell and Gene Therapy
Speaker: Edd Lee, Vice President, Global Sales and Marketing, Nabsys
Date: Wednesday June 18, 2025
Time: 12:00 PM - 1:00 PM PT
Location: UCSD - Leichtag Room 107 at 9500 Gilman Dr. La Jolla, CA 92093
Join us to learn how you can access electronic genome mapping and the OhmX™ in your research! Lunch will be provided for all registered attendees.
The laboratory workhorse for both structural variant verification and whole genome structural variant discovery
Utilizing state-of-the-art electronic nanodetectors, the OhmX platform detects tagged high molecular weight DNA molecules with unprecedented precision and speed offering a superior and reliable tool for structural variant analysis.
How does EGM work?
Watch this video to learn how electronic genome mapping works, including the step-by-step process of identifying structural variants, as well as the comprehensive bioinformatic analysis.
Resources
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OhmX Product Brochure
Overview of electronic genome mapping, how the technology works, product features, the bioinformatics and reporting pipeline, and key application areas.
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Rare Disease Case Study
Orthogonal verification of a tandem duplication suggested by short-read NGS with duplication breakpoints later estimated by optical genome mapping.
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Long Read Sequencing White Paper
This white paper explores how Electronic Genome Mapping (EGM) on the OhmX™ Platform—pioneered by Nabsys—can act as a powerful orthogonal validation tool for SV detection.