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PerkinElmer Genomics

Selects NxClinical Software

for Newborn Screening & Genomic Testing Services.

Los angeles

SoCal Region Cytogenetics & Molecular Genetics Meeting

Save the Date! 

January 9, 2019  |  City of Hope

More information to come...

Gold Standard

Gold Standard

Nexus Copy Number

Simple yet powerful tools for copy number (CNV) and sequence variation analysis and visualization from aCGH, SNP array, and NGS technologies (WES, WGS, targeted panels).

Nexus Copy Number Hero

The Power of One

NxClinical

A comprehensive software system for genetic data analysis and management for clinical labs, designed to improve productivity and patient care.

BioDiscovery Research and Clinical Software

Innovative genomic software tools to empower clinical & research labs to make the world a healthier place.

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Browse Our Range of Software Products

BioDiscovery provides the most comprehensive solutions for visualizing and interpreting genomic data for clinical labs as well as provides a complete set of user-friendly yet sophisticated analytical products for genomic research.

Customer Testimonials

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. Karine Hovanes, PhD, FACMG, Vice President of Scientific Advancement and Laboratory Director, Invitae
Dr. Karine Hovanes

Customer Testimonials

We were eager to be part of the Early Access program and try out NxClinical 4.1 Beta. We have 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 in version 4.1 as they make our interpretation process even easier.

- Dr. Sharon Mexal, Senior Director of Clinical Operations, Ambry Genetics
Dr. Sharon Mexal

Customer Testimonials

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. Matthew Breen, Professor, Genomics, Oscar J. Fletcher Distinguished Professor, Comparative Oncology Genetics
Dr. Matthew Breen, NCSU

Customer Testimonials

We have been using Nexus Copy Number and 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.

- Dr. Yajuan Liu, Assistant Professor, Department of Pathology, University of Washington
Dr. Yajuan Liu

Customer Testimonials

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. I have watched the progression of their software development from Nexus Copy number to NxClinical 4.1 and have always been satisfied with their improvements. BioDiscovery listens to their customers and utilizes this information to improve and refine their software for clinical laboratories. NxClinical 4.1 continues to be intuitive to use, has a searchable database, and has new desirable features. I now use NxClinical 4.1 to analyze CNV data from the CytoScan XON array. I am able to define gene panels and only analyze the genes from a targeted list. Also, I like that NxClinical can be used to analyze NGS data to make CNV calls and I am in the process of evaluating this new feature.

- Todd Ackely, Manager, Michigan Molecular Genetics Laboratory (MMGL)
Todd Ackely

Customer Testimonials

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. The combined analysis facilitates interpretation in particular with double hit events while allowing us to save resources. In addition, the ability of NxClinical to call CNVs from NGS is an added bonus that will allow us to replace multiple assays with a single NGS assay for interrogation of all genomic variants.

- Dr. Sarah Murray, Director of Genomics Technologies, UC San Diego
Dr. Sarah Murray

Customer Testimonials

The functionality of NxClinical has allowed us to simplify and standardize our interpretation of CNVs across our group of Directors. This significantly reduces the time required to review the 10+ variants identified per genome.

- Dr. Lawrence Jennings, MD, PhD, Director, HLA and Molecular Diagnostic Labs at Northwestern Medicine
Dr. Larry Jennings

Who We Work With

Ambry Genetics logo
MD Anderson
Baylor College of Medicine
NIH colored logo

Why BioDiscovery?

Versatility

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

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Top Notch Support

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

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Gold Standard for CNV Calling

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

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Featured Updates

blog-icon-e1489010952596

November 5, 2018

press
BioDiscovery’s NxClinical software augments PerkinElmer Genomics newborn screening and genomic testing services in labs around the world
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blog-icon-e1489010952596

October 25, 2018

blog
ASHG 2018 Wrap-up
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seattle

April 2-6, 2019

Events
April 2 – 6, Seattle, WA, Annual Clinical Genetics Meeting (ACMG) 2019
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blog-icon-e1489010952596

July 27, 2018

blog
Southern California Regional Cytogenetics & Molecular Genetics Meeting Proves to be Big Success
Read More