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

August 7-9, Denver, Colorado, Cancer Genomic Consortium...

Come see us at the Cancer Genomic Consortium Annual Meeting (CGC) 2017!

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

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