Mastermind uses AI-driven genomics to accelerate variant interpretation, providing immediate insight into the full text of millions of scientific articles. Mastermind prioritizes your search results by clinical relevance and finds what you are looking for 5-10 times faster.
REDUCE TURNAROUND TIME
Quickly identify and review the empirical evidence, clinically prioritized with insight into each article to speed variant interpretation
INCREASE DIAGNOSTIC YIELD
Mastermind has 100X more genomic evidence and 20X more variants than other sources to help you find relevant articles and upgrade VUS calls
Scale your caseload and reduce the risk of missing a patient diagnosis —save 60-90 minutes per VUS search on average with Mastermind
Rady Children’s Institute for Genomic Medicine uses Mastermind
Read the inspiring story of how this world-class institute used Mastermind to make a life-changing diagnosis for a sick newborn.
READ THE MASTERMIND STORY
Mastermind identifies every Genomic Association in the medical evidence, drawing informative connections between genes, variants, diseases, phenotypes, therapies, copy number variations (CNVs), and categorical keywords to inform both clinical care and drug discovery. Users can find, connect, explore, and understand the links between genomic concepts of interest in Mastermind’s intuitive literature search interface.
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In just 3 years, Mastermind surpassed the two primary sources of genomic literature, and we continue to add new data weekly! Here is a snapshot comparison.
|Full-Text Articles Indexed||8,337,455||86,000||86,756||28,175|
|Supplemental Datasets Indexed||3,017,170||N/A||N/A||N/A|
|Free Version Content||Up to Date||3 Years Old||Up to Date||Up to Date|
|Interpretation Criteria||ACMG/AMP||Own Criteria||ACMG/AMP||AMP|