In this guided training hosted by Genomenon, we’ll dive into genomic analysis with an expert curator and an experienced variant scientist who will demonstrate how they utilize the Mastermind Genomic Search Engine to rapidly classify variants with all relevant evidence. Driven by common questions from users, we will highlight helpful tips and tricks for navigating the literature with the world’s most comprehensive source of genomic evidence so that you get the most out of your data.
The Mastermind® Genomic Search Engine is the first source for variant interpretation of cancer and germline disease, using an AI-driven approach to connect patient genetic data with relevant evidence from scientific literature. The world’s most comprehensive source for genomic evidence, Mastermind is used by over 1,000 diagnostic labs and integrated into 18 clinical-grade decision support platforms and reference databases across the globe.
You will learn how to:
- Use Mastermind’s powerful Genomic Language Processing (GLP) algorithm to gain actionable insights from all published articles related to your search.
- Reduce turnaround time and increase diagnostic yield with clinical prioritization and in-text evaluation functionalities.
- Scale your caseload with advanced features such as protein-centric searching, genomic associations, ACMG/AMP criteria filtering, and alerts.
If you don’t yet use Mastermind, you’ll want to familiarize yourself before the webinar. Make a free account here and begin exploring on your own—you’ll be glad you did.