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CHARACTERIZING TARGETED CANCER THERAPIES via a COMPREHENSIVE GENE FUSION DATABASE
Who we serve…
PHARMA
Optimize drug discovery and translational targets with a comprehensive biomarker landscape from the literature
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CLINICAL DIAGNOSTIC LABS
Accelerate NGS variant interpretation with rapid search and deep insight into the full-text genomic literature
LIFE SCIENCES
Perform genomic research and Identify evidence-based biomarkers for NGS panel and assay design
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What we do…
MASTERMIND GENOMIC SEARCH ENGINE
Search 30 million papers for associations and get deep insight into the full-text for faster, more comprehensive variant interpretation
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GENOMIC BIOMARKER IDENTIFICATION SERVICE
Identify and prioritize genomic biomarker candidates for drug development and NGS panel design with a comprehensive evidence-based report, powered by Mastermind
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GENOMIC DATA LICENSING
Access Mastermind’s comprehensive database of published genomic biomarkers, including all literature citations for any disease
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API AUTOMATION
Automate your variant interpretation workflow with customized APIs via a direct connection to Mastermind
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See how the Mastermind Genomic Search Engine
finds disease-gene-variant associations by significance from medical sources
Powered by our comprehensive meta-database built from:
Full-text Publications
&
Mastermind Database
Our Partners
Learn More About Mastermind
Faster Searches
Mastermind provides prioritized, clinically relevant searches across millions of genomic articles.
Full Text Indexing
Unlike PubMed which only searches titles and abstracts, Mastermind provides full text indexing.
Deep Insight
Full text sentence matches for gene, variant, and keywords give you deep insight to each article.
More Comprehensive
Mastermind’s simple search interface finds articles for every disease, gene and variant you search.
Highlighted Content
Quickly narrow your search with the number of times a gene or variant is found in each article.
Automation Capabilities
Workflow automation for gene and variant curation is a snap with the Mastermind API.
I can say with certainty that without the findings obtained from Genomenon, I would not have been able to provide a diagnosis for this patient.
Genomenon’s methodology improved the efficiency and completeness of our literature review process.
I don’t consider a patient’s report complete unless every variant has been researched through Mastermind
We are able to cast a wider net and pick up the most clinically relevant articles with the full text search capabilities of Mastermind.
Mastermind Alerts keeps us up to date on every new genomic publication related to reproductive medicine.
We looked for the best tools to accelerate literature curation and found there is no comparable solution in the market like Mastermind
