BioDiscovery

NEW – NxClinical 4.0

Bringing together cytogenetics and molecular genetics into one system for analysis and interpretation of all genomic variants from a single NGS assay.

CNV from NGS  |  Virtual gene panels  |  Enhanced filtering schemas
and more…

 

Why Choose NxClinical?

Demo | Features & Benefits | Resources

NxClinical 4.0 is the first comprehensive case review and reporting system for analysis and interpretation of all genomic variants from a single NGS assay. Powered with the gold-standard CNV calling algorithm for deriving copy number from NGS NxClinical 4.0 allows consolidation of tests to provide CNV, AOH, and Seq Var from a single platform increasing production efficiencies and the diagnostic yield.

The system also handles microarray data and scales and grows as a lab expands its offerings, eliminating the time consuming and costly process of training the staff on multiple software systems, maintaining separate databases, and manually integrating test results for a single sample.

Features & Benefits

Automatically builds a case history of all samples analyzed

Multi-user system with audit trail and global accessibility

database-icon

Maintains data fidelity with a secure, central database

Support for all major instrument vendors for both NGS & microarray

Simultaneous review of sequence variants, AOH, and CNVs

Copy number estimation from NGS using the gold standard in CNV calling

Customized workflows with adherence to ACMG or other guidelines

Single test paradigm – CNV, AOH, and sequence variants from NGS

Increased efficiencies across all areas saves time and money

Request a Personalized Demonstration

Why Choose BioDiscovery?

BioDiscovery provides a full line of modular software packages. These products empower Biologists and Geneticists with sophisticated, yet highly usable tools to analyze and interpret their data and draw meaningful conclusions.

Versatility

Able to handle and process data from all commercial platforms.

Efficiency

Optimum usage of computing.

Acute Sense of Fitness for Purpose

Usefulness to our community of users.

These products empower Biologists and Geneticists with sophisticated, yet highly usable tools to analyze and interpret their data and draw meaningful conclusions.

*This software is designed to assist clinicians and is not intended as a primary diagnostic tool. It is each lab’s responsibility to use the software in accordance with internal policies as well as in compliance with applicable regulations.

*NxClinical uses the Human Phenotype Ontology. Find out more at http://www.human-phenotype-ontology.org.