NxClinical Software Display VD Tab



NxClinical Software Display VD Tab

The most comprehensive and up-to-date solution for cytogenetics and molecular genetics in one system for analysis and interpretation of all genomic variants from microarray and NGS data.

Product Details


Nexus Copy Number

User-friendly and Powerful Statistical Tools
Product Details

Dr. Karine Hovanes, PhD, FACMG

Vice President of Scientific Advancement and Laboratory Director, Invitae

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.


Dr. Sharon Mexal

Senior Director of Clinical Operations, Ambry Genetics

We were eager to be part of the Early Access program and try out NxClinical. We have now been using NxClinical for many years and each release has features that we find really useful. BioDiscovery has also been very receptive to feedback from us on feature requests and we are happy to see many of those implemented as they make our interpretation process even easier.


Dr. Matthew Breen

Professor, Genomics, Oscar J. Fletcher Distinguished Professor, Comparative Oncology Genetics

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.


Dr. Yajuan Liu

Assistant Professor, Department of Pathology, University of Washington

We have been using Nexus Copy Number and are 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.


Todd Ackely

Manager, Michigan Molecular Genetics Laboratory (MMGL)

My CAP/CLIA clinical lab has used BioDiscovery CNV software since 2012. I have evaluated many CNV analysis software programs and the BioDiscovery software always has been the best choice for my lab. BioDiscovery listens to their customers and utilizes this information to improve and refine their software for clinical laboratories.


Liqiang Song

Be Creative Lab

NxClinical software allows us to comprehensively analyze CNV,LOH and sequence variants together. The local database functionality has provided a lot of valuable experience for us. We can directly access up-to-date integrated database within NxClinical software and add tracks to the genome browser for clinical analysis requirements.


Dr. Sarah Murray

Director of Genomics Technologies, UC San Diego

At the UCSD clinical genetics lab, we are tasked with providing a complete and clinically actionable genomic profile of a patient’s tumor. NxClinical allows us to do this rapidly and comprehensively by allowing us to consider CNV, LOH, and sequence variants together within a single software.


Dr. Rhea Behlmann, PhD, FACMG

Clinical Laboratory Director, Invitae

I have used NxClinical software for analysis and detection of deletions, duplications, and AOH regions from microarray data as well as NGS data for panels, exomes, and genomes. It is easy to transition between NGS and microarray analysis because the NxC platform is intuitive and easy to use and because the user interface is visually consistent regardless of data origin.

Rhea Behlmann (1)

FEATURED Customer Webinar

Copy Number Variant Detection by NGS: Coverage, Uniformity & Resolution


Presented by: Dr. Fen Guo, Ph.D., FACMG, FCCMG, Clinical Laboratory Director, PerkinElmer Genomics

Dr. Fen Guo, PerkinElmer Genomics

Who We Work With

Why BioDiscovery?

Platform Versatility

Able to handle and process data from all commercial platforms and multiple technologies.

Top Notch Support

We pride ourselves on delivering expertise and individual support for all products and services.

Industry-Leading CNV Calling

With 20+ years in the field of genomics, we pride ourselves on reliability and innovation.

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