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Real World Evidence

Unlock literature-driven real-world evidence to accelerate development, expand disease insights, optimize trials, and bring precision therapies to patients.

Real World Evidence

Genetic Disease Sponsorship

Provide clinicians and researchers open access to curated genetic evidence, reducing diagnostic barriers while advancing awareness, recognition, and scientific understanding.

Genetic Disease Sponsorship

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Software Solutions

Explore our platforms for germline and somatic variant interpretation.

Access article information on more than 26 million variants, as well as curated germline variant content.

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Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials.

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Services

Partner with our team of experts to create Tailored Solutions for your unique needs

Clinical Diagnostic Services

Data

Gain access to an expansive, constantly updated database of curated genomic information

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Video Tutorial

Welcome to Mastermind CORE powered by Genomenon

Welcome to Mastermind CORE powered by Genomenon. – the world’s most comprehensive genomic intelligence platform, trusted by researchers and scientists worldwide! In this video you will learn how you can leverage Mastermind CORE to connect you directly to the most relevant, actionable insights for patient diagnosis, precision therapeutics and drug discovery.In this video, you will learn to:

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🔎 Effortlessly search by gene, variant across nomenclatures

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🧬 Access expertly curated gene-disease relationships, provisional variant classifications, articles for copy number variants and more…

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📄 Explore indexed content from peer reviewed literatureWhether you are a clinical geneticist or a pharmaceutical scientist, Mastermind empowers you to leverage genomic data to enhance your diagnosis and accelerate the future of precision medicine.

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The World’s Most Comprehensive Source of Genomic Evidence

Mastermind accelerates variant interpretation with immediate insight into the full text of millions of scientific articles. Prioritize your search results by clinical relevance and find what you are looking for 5-10 times faster

Explore Mastermind CORE
Every Missing Genetic Variant is a Patient Your Label Doesn't Reach
  • Rare disease and precision oncology programs rely on evidence fragmented across millions of published articles and supplemental datasets.
  • Genomenon builds the custom real-world evidence your program needs.
  • AI-powered search. Expert scientific curation.
  • The result: a broader label, more eligible patients, and a regulatory filing your team can defend.
Request a custom evidence build for your program
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