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).

Get the first look

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.

BLOG

Labs Meeting a Minimum Standard of Data Sharing Identified...

July 20, 2017

How does clustering work in Nexus Copy Number?

June 29, 2017

Recent advances in research: Next generation sequencing...

June 22, 2017

Clinical

N_xClinical

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).

Learn More

Our Clients

BioDiscovery, Inc.
715 North Douglas Street
El Segundo, CA 90245
Tel: (310) 414-8100
Fax: (310) 414-8111

Nexus Copy Number 9.0 is here!

Clinical

A comprehensive genomic software.

Research

Elegant UI & powerful, statistical tools.

Our Clients

Nexus Copy Number provides a tremendously versatile means to integrate and interrogate data derived from multiple formats within a single interface.

Rachael Thomas

The functionality of NxClinical has allowed us to simplify and standardize our interpretation of CNVs across our group of Directors. This significantly reduces the time required to review the 10+ variants identified per genome.

Lawrence Jennings

Nexus Copy Number is a powerful tool in our workflow, allowing direct visualization of data from numerous platforms, with a graphical interface that is as appealing as it is informative.

Matthew Breen

The BioDiscovery support team provides a rapid and informative response to customer questions, which enables us to continually refine our analytical pipelines to meet our evolving needs.

Rachael Thomas

Adoption of the NxClinical software has provided an efficient and secure workflow for our data batch loading and processing at our high volume clinical laboratory.

Karine Hovanes

A key attribute from our perspective is that Nexus Copy Number readily caters for the needs of those working with custom-designed microarray platforms and the genomes of non-traditional species.

Rachael Thomas

We have been using Nexus Copy Number and very happy with it. It allows direct visualization of data from different platforms with informative graphical interfaces. We integrated this powerful tool in our workflow.

Yajuan Liu