Comprehensive and up-to-date decision support solution for cytogenomics and molecular genetics to assist with the analysis and interpretation of genomic variants from microarray and NGS data.
With the NₓClinical software, you get:
NₓClinical offers multi-platform integration by:
Bionano is committed to providing:
See how PerkinElmer Genomics uses the power of NₓClinical’s capabilities to call CNVs from NGS.View Webinar
Read more about homologous recombination deficiency and how Bionano NxClinical software provides in-depth analysis of HRD.Read White Paper
Learn how Ambry Genetics used NxClinical software to increase their case review efficiency by 5X.Review Case Study
Schedule a time to review the software to see how it can detect and analyze genome-wide variations.Request a Software Demo