BioDiscovery

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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Clinical

NxClinical

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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Research

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

CUSTOMER PUBLICATIONS

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

EVENTS

June 22 - 24, Cambridge, UK, Curating the Clinical...

We'll be at the Curating the Clinical Genome - ClinGen/DECIPHER 2016 Meeting in the UK!

NEWS

Ambry Genetics Selects BioDiscovery’s NxClinical...

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

Webinar Recording Now Available

Get copy number results from WES, WGS, and targeted panel NGS with Nexus Copy Number

Learn two methods to obtain copy number results from NGS data and view with sequence variants, with pair matched normals or with pooled normals.

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EDUCATIONAL VIDEOS

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.