The Next Evolution of Genomics

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.

Nabsys has partnered with Hitachi High Tech to develop and release the Human Chromosome Explorer™ (HCE), a suite of secondary analytical software tools that seamlessly assembles genomes and identifies SVs according to custom parameters. The Human Chromosome Explorer puts actionable SV data at your fingertips.