BioDiscovery

NxClinical 3.0

Sequence Variants & Copy Number Variants Unite

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CUSTOMER PUBLICATIONS

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

EVENTS

March 22 – 24, Phoenix, AZ, Annual Clinical Genetics...

Stop by our booth to see a demo of our latest version of NxClinical 3.0.

NEWS

BioDiscovery to announce NxClinical 3.0, a new software...

NxClinical 3.0 will be launched during the ASHG 2016 Meeting, October 18-21 in Vancouver, BC, Canada

WEBINAR RECORDING

Uniting CNV, AOH, and SV events in a Single Software System – NxClinical 3.0

This webinar is geared towards those who are analyzing CNV, AOH, and SV events and would like a single software system to unite them.

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