BioDiscovery

New Partnership With Illumina

Illumina Selects NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq™ Assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs

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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.

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Our Clients

CUSTOMER PUBLICATIONS

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

EVENTS

May 19- 20, Toronto, Canada, Great Lakes Cytogenomics...

Come see us at the Great Lakes Cytogenomics Conference (GLCC) 2016!

NEWS

Illumina Selects BioDiscovery’s NxClinical Software...

Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation...

Webinar Recording Now Available

Get copy number results from WES, WGS, and targeted panel NGS with Nexus Copy Number

Learn two methods to obtain copy number results from NGS data and view with sequence variants, with pair matched normals or with pooled normals.

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EDUCATIONAL VIDEOS

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.