BioDiscovery NxClinical - Comprehensive and Up-to-date Solution for Cytogenetics and Molecular Genetics
The most comprehensive and up-to-date solution for cytogenetics and molecular genetics in one system for analysis and interpretation of all genomic variants from microarray and NGS data.
- Increase the efficiency of your case review using the new Variant Details Tab
- Integrated automated ACMG CNV interpretation scoreboard
- One-click Uniparental Disomy (UPD) detection, visualization, and reporting
- Create your own bespoke Knowledgebase to store variant and genomic region information
- Build and utilize genome-wide CNV and AOH profiles for different cancer types to assist in tumor diagnosis and interpretation
- Don't leave past data behind - Automatic In-house case history & integrated genetic databases
- Different platforms? NxClinical can do it all
- Multi-user system with audit trail and global accessibility
- Security - Maintains data quality and integrity
- Speed to Decision - Faster TAT with automation, AI, and variant prioritization tools
- Increase clinical utility and diagnostic yield
First step is to detect the CNVs. You can’t diagnose what you can’t see. NxClinical is the gold standard for calling CNVs from NGS and microarray data generated on any platform.
Context is everything! NxClinical provides integrated analysis and raw data visualization of CNV, SeqVar, and AOH simultaneously, on the same screen for each patient sample.
Make the right call in record time. AI driven tools and extensive automation for rapid and accurate interpretation. Active links to the latest databases keep your knowledge base fresh and up-to-date.