Products
NxClinical
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.
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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
Position
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
Position
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
Position
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
Position
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
Position
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
Position
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
Position
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.
Upcoming 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.
Beginning Tuesday, May 18th, 3:00 PM CST
Who We Work With
Featured Updates
December 10, 2020
Increasing the yield of exome sequencing with copy number variant analysis
Read MoreApril 20, 2020
BlogPromising results for a new non-invasive prenatal test that uses single circulating trophoblasts
Read MoreSeptember 10, 2019
pressBioDiscovery Designates Children’s Hospital of Los Angeles as a Center of Excellence for Clinical Genomics
Read MoreApril 18, 2019
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