NxClinical 3.0 will be launched during the ASHG 2016 Meeting, October 18-21 in Vancouver, BC, Canada
Ambry Genetics selects BioDiscovery’s NxClinical software for analysis, management, and reporting of copy number events in its clinical genomics workflow.
Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq ™ assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs
Nexus Copy Number 8.0 is derivation of copy number from NGS results. BAM (pooled reference), detects copy number from WES, WGS, and targeted NGS panels.
CombiMatrix is now using BioDiscovery’s NxClinical software for analysis, management, and interpretation of copy number events in its clinical workflow.
Recognized leader in research and education, and one of the top pediatric providers in the Midwest recently started using NxClinical.
See how Nexus Copy Number has been used at North Carolina State University to detect copy number changes by CGH analysis in Canines.
A genomics services provider for clinical trials, testing, and research will now be working with BioDiscovery in a co-marketing partnership.
NxClinical 2.0 is a flexible, platform-agnostic database solution for efficient analysis, interpretation, and reporting of variations.
NxClinical focuses on improving efficiency and quality through multi-user collaborative communication, audit-trail features, and automation.