Reduce Turnaround Time
Quickly identify and review the comprehensive empirical evidence, clinically prioritized with insight into each article to speed variant interpretation
Increase Diagnostic Yield
Access 100X more genomic evidence and 20X more variants than other sources to find relevant articles, resolve more VUSs, and diagnose more patients
Optimize your workflow by automating the acquisition and prioritization of genetic evidence with the Mastermind API
Are you confident you have all the information you need for variant interpretation?
A 2020 Study reported that laboratories disagreed on a variant’s classification 46% of the time, with 23% of those discrepancies being clinically impactful. Access to comprehensive evidence is critical for proper diagnosis.
GET STARTED NOW
Legacy Nomenclature Makes Evidence Hard to Find
More than 74% of the genomic variants in publications are still in non-normalized forms1, making citations hard to find
Data is Hidden in the Body and Supplemental Text
Fewer than 6% of variants are identified in the title or abstract, the remainder present in the full-text or supplemental files1.
Incomplete genomic evidence puts patients at risk
One paper can change everythingRead the inspiring story of how Rady Children’s Institute
for Genomic Medicine used Mastermind to make a
life-changing diagnosis for a sick newborn
READ FITZ'S STORY
Learn more about Mastermind in 60 seconds
|Full-Text Articles Indexed||9,194,607||72,987||106,833|
|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|