Webinars
Electronic Genome Mapping for Human Whole Genome Structural Variation Analysis
Explore how Electronic Genome Mapping (EGM) is redefining whole-genome structural variant analysis in this seminar from the 70th Annual Meeting of the Japan Society of Human Genetics.
Featuring experts from Nabsys and Harvard Medical School, this session dives into the science behind EGM, its high-resolution, cost-effective workflow, and real-world applications, ranging from rare disease discovery to repeat expansion analysis and cell line quality control.
See how EGM uncovers critical genomic alterations that traditional methods often miss—and discover why it’s becoming an essential tool for both research and clinical genomics.
To learn more, watch the presentation below!
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Cancer Research
Gain deeper insights and drive breakthroughs in cancer research with the OhmX™ Platform, powered by electronic genome mapping (EGM) and expertly engineered to unravel the complexities of structural variants (SVs) in cancer genomes.
Orthogonal Validation of NGS and LRS
Gain confidence in your genomic discoveries from NGS and long-read sequencing (LRS) platforms with a low-cost solution to verify, clarify, and identify structural variant (SV) calls.
Rare Disease
Unravel complexities and gain critical insights with the OhmX™ Platform, designed to help you push the boundaries of rare disease research.
Cell and Gene Therapy
EGM provides clarity to genomic integrity where other tools can’t.