BioDiscovery

NEW – NxClinical 4.0

Bringing together cytogenetics and molecular genetics into one system for analysis and interpretation of all genomic variants from a single NGS assay.

CNV from NGS  |  Virtual gene panels  |  Enhanced filtering schemas
and more…

 

CUSTOMER PUBLICATIONS

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

EVENTS

November 16 – 18, Salt Lake City, UT, Association...

Come see us at the Association for Molecular Pathology (AMP) Meeting! Visit us at booth #1605 to learn...

NEWS

BioDiscovery Inc. Forms Partnership with Be Creative...

BioDiscovery announced today an agreement with Be Creative Lab in Beijing, China to be the exclusive...

WEBINAR RECORDING

Downstream Research Analysis of Copy Number from NGS in Cancer Samples

This webinar is geared towards those working on research projects and want to know what types of advanced analyses can be performed in Nexus Copy Number.

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.

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, and NGS technologies (WES, WGS, targeted panels).

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Our Clients