Overview
About Nabsys
Electronic Genome Mapping
Setting a new standard in structural variant analysis
Nabsys, the pioneer of electronic genome mapping (EGM), uses solid-state nanodetectors to survey long DNA molecules to construct high-density maps with long-range information required to detect structural variants (SVs). Unlike other DNA mapping technologies that rely on the use of expensive optical imaging or fluorescent labels whose resolution is inherently limited by light diffraction, EGM identifies tags in close proximity therebye producing superior resolution. This high-density information makes it possible to identify both balanced and unbalanced SVs as small as 300 bp, in addition to larger chromosomal aberrations and genetic variation missed by next-generation sequencing. EGM involves simple, intuitive workflows eliminating the need for cytogenetics technical expertise, while delivering on the promise of easy-to-use, accurate, low-cost, whole-genome SV analysis.
Visit the new Nabsys: https://nabsys.com/
Meet the OhmX™ Platform: Explore the genome in high-resolution.
From sample prep through analysis, the OhmX end-to-end solution allows you to detect balanced and unbalanced events and a broad range of structural variants with precision.
High Resolution
Detection of SVs as small as 300 bp with >100 kb read lengths
Low Cost
Low instrument and consumable costs compared to other technologies
Small Footprint
Entire platform fits within 30"x17" saving valuable benchtop space
Easy to Operate
Easy sample prep, automated run monitoring & minimal hands-on time
Accessible Analytics
Web-based UI for data mining SVs via Human Chromosome Explorer™ powered by Hitachi High Tech
Setting a new standard in structural variant analysis
Nabsys, the pioneer of electronic genome mapping (EGM), uses solid-state nanodetectors to survey long DNA molecules to construct high-density maps with long-range information required to detect structural variants (SVs). Unlike other DNA mapping technologies that rely on the use of expensive optical imaging or fluorescent labels whose resolution is inherently limited by light diffraction, EGM identifies tags in close proximity therebye producing superior resolution. This high-density information makes it possible to identify both balanced and unbalanced SVs as small as 300 bp, in addition to larger chromosomal aberrations and genetic variation missed by next-generation sequencing. EGM involves simple, intuitive workflows eliminating the need for cytogenetics technical expertise, while delivering on the promise of easy-to-use, accurate, low-cost, whole-genome SV analysis.
Visit the new Nabsys: https://nabsys.com/
Meet the OhmX™ Platform: Explore the genome in high-resolution.
From sample prep through analysis, the OhmX end-to-end solution allows you to detect balanced and unbalanced events and a broad range of structural variants with precision.
High Resolution
Detection of SVs as small as 300 bp with >100 kb read lengths
Low Cost
Low instrument and consumable costs compared to other technologies
Small Footprint
Entire platform fits within 30"x17" saving valuable benchtop space
Easy to Operate
Easy sample prep, automated run monitoring & minimal hands-on time
Accessible Analytics
Web-based UI for data mining SVs via Human Chromosome Explorer™ powered by Hitachi High Tech