BioDiscovery 

The Power of One.

Analyze & Interpret of all genomic variants from a single NGS assay.

We can’t wait to share our secret…

NxClinical 4.1 is coming! 

Sign-up for our New Webinar: Dr. Sarah Murray, UCSD

 

THE LATEST BUZZ

ASHG Workshop Customer Presentation Series – Access Videos Here

Featuring: Dr. Ingrid Simonic, Dr. Ben Darbro, & Dr. Daynna Wolff

EVENTS

June 16 - 19, Milan, Italy, European Human Genetics...

Come see us at Stand #430 at the ESHG European Human Genetics Conference in Milan, Italy! Get an in-depth...

NEWS

Thermo Fisher Scientific and BioDiscovery form software...

BioDiscovery, a leader in copy number analysis software, created a new tailored software solution (Nexus...

NEW WEBINAR

Speaker: Dr. Sarah Murray, UCSD

Combined Analysis and interpretation of CNV, AOH, and Seq Var of FFPE cancer samples from a solid tumor NGS panel

This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.

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