BioDiscovery

NxClinical 3.0,
Coming Soon

Sequence Variants & Copy Number Variants Unite

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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

Oct. 18-22, Vancouver, CAN, American Society of Human...

Come see us at the American Society of Human Genetics Annual Meeting! We'll be in booth #1419!

NEWS

Ambry Genetics Selects BioDiscovery’s NxClinical...

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

VIEW WEBINAR RECORDING

Gene Prioritization in Regions of Homozygosity

Learn how regions containing genes known to be recessive and associated with the given phenotype can be quickly identified in a sample and how regions of homozygosity in one sample compare to other samples in the database.

EDUCATIONAL VIDEOS

Identification of Common Aberrations

Learn what aberrations are common, and two popular approaches (GISTIC and STAC) used to determine which are statistically significant.