The OhmX™ Platform: A Novel System for Whole-Genome Structural Variant Analysis

Structural variants (SVs) are a major source of genetic variation, influencing disease, gene expression, and genomic function. Despite decades of innovation, many SVs still go undetected due to the limitations of karyotyping, FISH, microarrays, and sequencing.

The OhmX™ Platform, powered by electronic genome mapping (EGM), delivers high-resolution, whole-genome SV detection that overcomes these challenges. With 300 bp resolution and desktop-sized instrumentation, OhmX provides scalable, cost-effective insights into the full spectrum of genomic variation.

In this poster, you’ll discover:

• How the OhmX™ Platform captures SVs across the genome, from insertions to inversions
• Direct comparisons of OhmX to cytogenetics, NGS, and long-read sequencing
• Genome-wide concordance with PacBio HiFi and ONT datasets
• A streamlined workflow supporting fresh or frozen cells, blood, and bone marrow
• Affordable, scalable SV detection — up to 130 genomes per year

By combining broad length-scale detection with orthogonal validation, the OhmX™ Platform complements sequencing technologies and delivers unprecedented clarity in genome analysis.

Download the poster now and see how OhmX is redefining whole-genome structural variant detection.