Electrify Your Structural Variant Detection
Making advanced genomics accessible, affordable, and impactful for every lab.
%20(1)%20(1).avif)
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.
.svg)
Repeat Expansion Detection and Confirmation
Detect and confirm complex repeat expansions with the OhmX™ Platform, delivering accurate sizing and structural insight beyond the limits of PCR and traditional sequencing methods.
