BioDiscovery to Announce release of NxClinical 3.0 at ASHG!

Latest Version of NxClinical Coming Soon

BioDiscovery will be releasing a NxClinical 3.0 at the American Society of Human Genetics 2016 Meeting.

With NxClinical you can stop using multiple software systems to analyze and report genomic variants, and start visualizing and interpreting copy number results, sequence variants, and allelic events from arrays and NGS using a single integrated user interface. NxClinical 3.0 will allow you to:

• Store and manage NGS data in addition to array data
• Visualize and interpret Copy Number and Sequence Variants side-by-side
• Expand lab capabilities without investing in additional software
• Replace multiple software pieces with one integrated solution

Attending ASHG and want to get a first look? Register for our lunchtime presentation.

Not attending ASHG but would like to learn more? Get the first look here.