Genomenon’s Mastermind Genomic Search Engine is recognized as a premier research tool in the genetic variant interpretation space. By identifying every genomic association within the existing literature and drawing informative connections between them, Mastermind’s patented algorithms are able to reveal hidden information that could lead to a research discovery or solving a clinical case. As a result, it’s more than just a database – it’s a virtual colleague.

In this presentation, Nisa Esen of Acibadem Labgen and Ariana Gonzalez of Héritas will share real-world cases where use of the Mastermind Genomic Search Engine led to more informed diagnosis and treatment decisions. Armed with combined experiences in rare disease exome sequencing, precision medicine, and diagnostic genetics, these speakers will describe how Mastermind is not only streamlining variant interpretation in their work, but is also driving their shared mission to advance human health outcomes for rare genetic diseases and cancer.

You will learn:

• What challenges both geneticists and clinical decision makers are currently facing surrounding genetic variant interpretation,
• How clinical practitioners are applying Mastermind in their work to streamline their workflow, and
• How both genetic research and clinical diagnostics are impacted by Genomenon’s AI-driven solution.

Introduction from Genomenon Founder and Chief Science Officer, Dr. Mark Kiel.