Whitepapers

Nabsys HD-Mapping™ System

The Nabsys HD-Mapping™ platform offers groundbreaking capabilities for high-definition whole-genome structural variation (SV) analysis. By employing electronic rather than optical detection, it captures both balanced and unbalanced SVs with unparalleled resolution, enabling detection of variations as small as 300 base pairs. The system’s innovative solid-state nanochannel technology minimizes costs while maintaining a compact, desktop-sized footprint, making it a cost-effective alternative to traditional cytogenetic techniques and long-read sequencing.

With features like real-time processing, a streamlined workflow, and integration with the Human Chromosome Explorer™ (HCE), HD-Mapping delivers comprehensive insights into genomic variations. It bridges the gap between short-read sequencing and optical genome mapping, providing researchers with a powerful tool for understanding complex genomic alterations across a wide range of applications, from constitutional disease to cancer research. Learn more at nabsys.com/learn/electronic-genome-mapping.

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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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