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CHICAGO (GenomeWeb) – Swiss precision medicine analysis company Saphetor and US-based genomic literature search engine Genomenon have announced a deal to share genomic variant information between their data platforms.

The companies said today that results from the Genomenon Mastermind genomic search engine now include links to Saphetor's VarSome genomic annotation tool. In turn, VarSome, which contains curated data from more than 30 publicly available genomic databases, has Mastermind links to scientific literature related to each variant and gene.

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Sponsored by
Bionano Genomics

This webinar will outline how a team at Radboud University Medical Center is assessing ultra-long read optical mapping on the Bionano Saphyr system to replace classical cytogenetics approaches in routine testing and for the discovery of novel structural variants with potential scientific, prognostic, or therapeutic value that are missed by standard approaches.

Oct
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Sponsored by
Swift Biosciences

This webinar will illustrate how single-cell methylation sequencing can be applied to gain significant insight into epigenetic heterogeneity in disease states, advancing cancer research discoveries. 

Oct
24
Sponsored by
Sunquest

This webinar will tell the story of Versiti’s journey in transforming genetic testing from a manual to a digitized process. It will include detail on how the organization succeeded, pain points along the way, a novel approach to variant assessment, and future plans for the program.