Bringing together cytogenetics and molecular genetics into one system for analysis and interpretation of all genomic variants from a single NGS assay.
NxClinical 4.1 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 4.1 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.
Learn more about NxClinical 4.1 here
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.
Able to handle and process data from all commercial platforms.
Optimum usage of computing.
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.