REDUCE TURNAROUND TIME
Quickly identify and review the 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
ACCELERATE YOUR THROUGHPUT
Optimize your workflow by automating the acquisition and prioritization of genetic evidence with the Mastermind API
Trusted by 20,000+ Users in 140+ Countries
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.
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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.
Mastermind Basic Edition is free. No credit card required. Get a free trial of Professional Edition when you sign up.
“How much does the Professional Edition cost?”
Our Mastermind Experts will find the right plan for your team.
Mastermind’s Genomic Language Processing finds all the evidence regardless of nomenclature. No need to guess!
“What if there are too many articles?”
Now that you have all the evidence, see step 3 to refine your search.
Refine your results with comprehensive filters such as ACMG criteria, clinical significance, genetic mechanism, and more.
“How do the filters work?”
Our tutorial videos and Customer Success team are here to help.
View sentence fragments to confirm article relevance. Quickly link out to the evidence for a deeper look.
“How can I be confident my results are comprehensive?”
A recent study showed that Mastermind is the most comprehensive source of published genomic literature. Read the paper.
Mastermind is integrated into your favorite software
I don’t consider a patient’s report complete unless every variant has been researched through Mastermind.
Using Mastermind enhances our ability to provide clinicians at the bedside with important relevant information about known treatments and interventions.
I can say with certainty that without the findings obtained from Mastermind, I would not have been able to provide a diagnosis for my patient.