Nexus Copy Number 8.0 Has Arrived!

The most comprehensive tool for producing copy number results from whole genome sequencing (WGS), whole exome sequencing (WES), or targeted panel NGS data.

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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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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.

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Our Clients


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


March 9 – 11, Tampa, FL, Annual Clinical Genetics...

Come see us at the Clinical Genetics Meeting, booth #317! You can receive a free portable phone charger...


Product Release: Nexus Copy Number 8.0

With a new version of Nexus Copy Number available, you can now get copy number results from whole genome...

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Detecting CNVs from Whole Exome Sequencing Data Using Nexus Copy Number  – December 8th, 2015

Learn a new way of inferring CNVs from whole exome sequencing data using nexus copy number software, and also see how this method compares to other methods.

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ASCAT Algorithm

Learn what the ASCAT algorithm does and how it accounts for complications of aneuploidy, tumor heterogeneity, and contamination from normal cells in tumor sample analysis.