BioDiscovery

Nexus Copy Number 9.0 is here!

Get copy number results from whole genome (WGS), whole exome (WES), and targeted panel sequencing data from a new method called BAM (multiscale reference).

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CUSTOMER PUBLICATIONS

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

EVENTS

May 27 - 30, Copenhagen, Denmark, European Human Genetics...

Come see us at Stand #124 at the ESHG European Human Genetics Conference in Copenhagen, Demark! Get an...

NEWS

BioDiscovery releases Nexus Copy Number 9.0 with improved...

The new features in Nexus Copy Number 9.0 really enhance the usability of WES, WGS, targeted panels and...

WEBINAR RECORDING

Challenges and Solutions to Copy Number Estimation from Whole Exome Sequencing in Tumors

Join us as Research Scientist Shawn Anderson discusses how he gets copy number results from low coverage sequencing results (shallow/targeted) and/or from normal coverage WGS/WES results.

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