Clinical Research Software For Genomics

Our software detects CNVs and AOH/LOH from NGS and/or microarrays and then displays them along with SNVs.

Products

N_xClinical

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

Dr. Karine Hovanes, PhD, FACMG

Vice President of Scientific Advancement and Laboratory Director, Invitae

Adoption of the N_xClinical 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 N_xClinical. We have now been using N_xClinical 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

N_xClinical 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 N_xClinical 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. N_xClinical 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.