Research and Clinical Genomics Software

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Research and Clinical Genomics Software

BioDiscovery detects CNVs from NGS and/or microarrays, displays them along with SNVs allowing maximum info to guide the best decisions that influence patient outcomes.

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.

Testimonial Invitae

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.

Testimonial Ambry Genetics

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.

Testimonial NC State University

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.

Testimonial University of Washington

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. 

Testimonial University of Michigan

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.

Testimonial Be Creative Lab Bejing

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.

Testimonial UC San Diego

Recent Customer Webinars

The Variant Interpretation Virtual Symposium

Hear from clinical genomic leaders as they present variant interpretation best practices through case studies and real-life validations across a variety of applications that aided in the improvement of their laboratory output.

Who We Work With

Ambry Genetics logo
Invitae logo
Erasmus MC
Lurie Children's Hospital logo
Baylor College of Medicine
be creative colored logo
Addenbrooke's NHS
Children's Mercy Kansas City
UC San Diego
MUSC - Medical University of South Carolina
Universität Zürich
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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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