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OhmX Brochure

Revolutionize your structural variant (SV) analysis with the OhmX Platform, powered by Electronic Genome Mapping (EGM). This innovative technology uses solid-state nanodetectors to deliver high-resolution genomic insights, detecting SVs as small as 300 base pairs with unmatched precision. With its compact design, low costs, and user-friendly workflow, OhmX streamlines whole-genome analysis for researchers, eliminating the need for advanced cytogenetics expertise.

Perfect for applications in cancer research, rare disease studies, cell and gene therapy, and personalized medicine, the OhmX Platform offers scalable, cost-effective solutions. Its web-based analytics enable seamless data integration, making it easier than ever to explore genomic variations with accuracy and efficiency. Transform your research today with OhmX. Learn more at nabsys.com/products.

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Research Areas & Applications

Cancer Research
Genomic structural variations (SVs) encompass a diverse array of alterations involving large segments of the genome, such as deletions, duplications, inversions, translocations, and insertions.
Rare Disease
Structural variants are essential for diagnosing many genetic disorders and understanding their inheritance patterns.
Cell and Gene Therapy
In many patients, accurate detection and characterization of SVs are crucial for understanding disease etiology, developing targeted therapies, and designing effective gene delivery vectors.
Functional Genomics Research
DNA structural variations can impact gene expression and function. Identifying SVs is essential for deciphering the functional consequences of genetic variation.

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