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Genomenon : Announces Enhanced CNV Search Capabilities for Pharma

Genomenon Logo 2020 - stacked tag

Genomenon are excited to announce the launch of Copy Number Variation (CNV) enhanced search, furthering our ability to catalogue a complete dataset of all Genomic Associations supported by medical evidence. This new update to the Mastermind software suite of tools will help Pharma companies accelerate new discoveries in the development of treatments.

 
 
On Thursday, October 15th at 11am EDT, Genomenon co-founders, Chief Science Officer Mark Kiel, MD, PhD and Chief Technology Officer Steve Schwartz will take a use-case approach to highlighting the new CNV capability at the Mastermind Masterclass: CNV Search. Join us for the webinar to see how Genomenon provides genomic intelligence for Pharma.
 
 
 
CONNECT WITH GENOMENON:
 
 
Biomarkers for Rare Non-Oncological Diseases Summit
November 10-11, 2020
 
The 2nd Annual Biomarkers for Rare Non-Oncological Diseases Summit will unite biopharma, diagnostic and healthcare teams to advance the application of precision medicine in rare diseases beyond oncology. Connect with us at BM & Dx 2020 by visiting our virtual booth, or email us to schedule a meeting with our leadership team.
 
 
 
Explore and Discover!
The Genomenon Team
 
 
 
 
Connect With Us
Explore & Discover!
The Genomenon Team
 

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