BioDiscovery 

The Power of One.

Visualize, Analyze,  Interpret, & Report all genomic variants from a single NGS assay.

NxClinical 4.1

Learn More

 

THE LATEST BUZZ

Optimizing and Consolidating Multiple Testing Strategies to Increase Efficiency with Increasing Testing Demand

Clinical Conversation: Dr. Ingrid Simonic, Medical Genetics Laboratories, Cambridge University Hospitals, UK

EVENTS

Aug. 4 -7, Sydney, AUS, Human Genetics Society of Australia...

Come see us at the Human Genetics Society of Australia! We'll be in booth #19!

NEWS

BioDiscovery releases Nexus Copy Number 10.0, a single...

Nexus Copy Number 10.0 is a highly robust, intuitive, and multi-platform software for both copy number...

WEBINAR RECORDING

Speaker: Dr. Sarah Murray

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.

Learn More

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).

Learn More

Our Clients