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We had a great time at the Annual Clinical Genetics Meeting in sunny Phoenix, AZ last week!  It was great seeing so many new faces, friends, and colleagues at our booth, where BioDiscovery presented the latest version of NxClinical 3.0.  NxClinical 3.0 is the first comprehensive case review and reporting system that expertly handles both array and NGS generated data in a single repository offering a complete view of a sample under review.IMG_2268.jpg

We also presented a poster, “Seeing the Whole Picture – Integrated View of CNVs, AOH, and Sequence Variants Leads to Improved Results”, which reviews an interesting in case in detail. A complete comprehensive semi-automated workflow is described, which takes us from raw data to a final interpretation report using NxClinical 3.0 for integrated copy number and sequence variant analysis within a proband.

Finally, a big thanks to all attendees for our highly-attended exhibit theater. Dr. Soheil Shams presented an overview of the many functions and capabilities of NxClinical 3.0 and took us through a live review of several samples. The presentation and software were very well received, along with a one-of-a-kind BioDiscovery T-shirt for all attendees.

Looking forward to ACMG 2018 next year!

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