Ambry Genetics Selects NxClinical Software

Ambry Genetics® has migrated its data management, analysis and interpretation of copy number changes to NxClinical software.

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A comprehensive genomic software.

It is the world’s most comprehensive tool for genetic data analysis and management for clinical labs, designed to improve both productivity and patient care.

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Nexus Copy Number

Elegant UI & powerful, statistical tools.

Nexus Copy Number software offers simple yet powerful tools for copy number (CNV) and sequence variation analysis and visualization from aCGH, SNP array.

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Our Clients


Find educational research publications provided by our customers, or submit your own.


August 8-10, Denver, CO, Cancer Genomics Consortium...

We'll be attending the Cancer Genomics Consortium (CGC) 2016 and we hope to see you there!


Ambry Genetics Selects BioDiscovery’s NxClinical...

Ambry Genetics selects BioDiscovery’s NxClinical software for analysis, management, and reporting of...

Webinar Recording

Integrated analysis of copy number, sequence variant and gene expression data in cancer cohort

Learn about analyzing DNA copy number variants and sequence variants, as well as the option to integrate associated RNA expression results on both the aggregate and single sample levels.


ASCAT Algorithm

Learn what the ASCAT algorithm does and how it accounts for complications of aneuploidy, tumor heterogeneity, and contamination from normal cells in tumor sample analysis.