Electrify Your Structural Variant Detection

A comprehensive solution for amplification-free DNA analysis, enabling researchers to progress from sample to genome mapping on the OhmX Platform in a single day.

Analyze up to 30 genes with RepX Analysis for Repeats Expansion Disorders

Structural variants (SVs) are the dominant form of genomic variation and make up over 1% of the human genome. To fully realize the promise of genomics and improve human health, researchers and clinicians must query and understand all forms of SVs.

The OhmX Analyzer is a simple benchtop solution designed to drive SV detection at the whole genome level. With its low cost and minimal set-up requirements, researchers and scientists can now conveniently access SV data, without compromising on sensitivity and accuracy.

Our state-of-the-art, electronic nano-detectors deliver the highest resolution for whole genome structural variant analysis. With the analyzer, you can perform whole genome analysis of SVs down to 300bp in size—enabling insights into previously undetectable DNA variations.