The laboratory workhorse for both structural variant verification and whole genome structural variant analysis
The OhmX Analyzer utilizes state of the art electronic nanodetectors to detect tagged high molecular weight DNA molecules with unprecedented precision and speed offering a superior and reliable tool for structural variant analysis.
Ultra-long range genomic information
detection of structural variants as small as 300 bp
Low capital equipment costs
Sample loading port constructed for easy injections allowing for walkaway automation by repeatedly introducing the sample through the microfluidics manifold to the nanodetector throughout the run
Nanodetector carriage precisely aligns the detector with the microfluidic sample introduction path
Waste is automatically collected and software alerts instruct when to remove
Cartridges contain preformatted, ready-to-use reagents for cleaning, washing, and running experiments on the solid-state nanodetectors with volumes automatically managed by software
Precisely tuned electronics eliminate sources of noise increasing throughput of high quality electronically detected tagged HMW DNA molecule data
Entire platform sits within a 30”x 17” space
Our algorithms improve results by using more of the available data to build more accurate consensus maps and make more SV calls
Built in the Google cloud, HCE benefits from the very latest and best encryption and cloud security
There is no limit to the dynamic compute resources that can be allocated to a project bringing analysis times down to a few hours and enabling you to process many samples simultaneously
Our intuitive web-based user interface allows you to upload, run, and analyze results without bioinformatics expertise or support
HCE lives in the cloud so there is no need for expensive hardware or related human resources
60 Clifford Street
Providence, Rhode Island
02903 USA
Phone: 401.276.9100
Fax: 401.276.9122
info@nabsys.com
Advance the understanding of disease, increase diagnostic yield, and improve patient outcomes by enabling routine, accurate, cost-effective analysis of genomic structural variation
