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.
Quickly find all relevant articles for your specific search criteria, covering every disease, therapy, phenotype, gene, and variant.
Find hidden data and prioritize your results with intelligent tools that bring the most relevant articles to the top for review.
Search beyond title and abstract into the complete text of every published genomic paper, including supplemental data.
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.
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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||9,342,310||72,987||108,063|
|Supplemental Datasets Indexed||3,182,337||N/A||N/A|
|Free Version Content||Up to Date||3 Years Old||Up to Date|
|Interpretation Criteria||ACMG/AMP||Own Criteria||ACMG/AMP|
|ACMG Gene Curation Parameters||YES||NO||NO|
|Clinical Exome Genes Curated based on ClinGen recommendations||YES||NO||NO|