BioDiscovery

NxClinical 3.0

Sequence Variants & Copy Number Variants Unite

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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

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

NEW WEBINAR

A new method to estimate copy number from NGS for both shallow/targeted sequencing and WGS/WES data

This webinar is geared towards those requiring copy number results from low coverage sequencing results (shallow/targeted) and/or from normal coverage WGS/WES results.

EDUCATIONAL VIDEOS

Data QC

Learn about the different quality measures, how the quality score is calculated, and how to determine what is a good quality score.