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Built for the Needs of Your Industry
Be 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.
Reduce Turnaround Time
Explore our continually growing catalog of pre-classified variants, designed to facilitate the rapid uncovering and interpretation of novel genetic variations.
Access valuable gene and variant summary information to streamline your analysis and deepen your insights.
Increase Diagnostic Yield
Gain confidence in identifying more disease-causing variants leveraging our Genomic Intelligence Platform.
Our genomic language processing technology empowers you to uncover more disease-causing variants with precision.
Accelerate Throughput
Optimize your workflows by rapidly prioritizing variants of disease-causing genes.
This efficient process reduces resources, simplifying your analysis and enabling a more targeted approach.
The Mastermind Genomic Intelligence Platform
Mastermind gives you access to all the information that's available on your disease of interest already curated and ready to go.
You can search by variant, gene, disease, therapy, and more. Mastermind contains the full text of more than 9.5 million publications, which are easily searchable by gene, variant, disease, and other key terms.
Save Time and Minimize Expenses
Expedite your research workflow with instant access to the entirety of genomic research, pre-annotated by gene, variant, disease, and therapeutic.
Accelerate Trial Eligibility Decisions
Get the information you need to make an educated decision faster through an easy-to-use search interface that returns prioritized, filterable literature results for identified variants.
Characterize and Prioritize Targets and Programs
Accelerate research on potential targets and programs through prioritized and filterable literature results for the gene and/or disease of interest.
Thousands of labs are using Mastermind to increase diagnostic yield.
Start searching the world's most comprehensive source of genomic evidence. Create your free account today.
Features
Gene Profile Page
The Gene page allows users to access essential information from a variety of sources like ClinVar, ClinGen, DECIPHER, and gnomAD. Researchers can enhance their productivity by accessing details about {manually curated} gene-disease relationships, variant types, pathogenicity, and gene summaries all in one place.
From the gene page, users can seamlessly go to article searches and access data from Genomenon’s curated content and public sources like ClinVar.
Variant Evidence Page
Discover our enhanced Evidence page designed to streamline information, allowing users to efficiently prioritize, navigate, and explore insights on search parameters of interest.
Mastermind makes it easy by including sentence fragments where the search terms were found in the article. With improved speed and workflow, researchers can effortlessly access and search through articles and curated content.
FAQ
Find answers to all of your pressing Mastermind questions here.
Mastermind Plans
Interested in a somatic variant knowledgebase?
CKB is the standard in evidence-based interpretation of complex cancer genomic profiles.
Learn more about Mastermind's capabilities for clinical diagnostics and precision therapeutics.
