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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

A computer in a clinical lab using Mastermind genomic database software.

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.

Meet Mastermind

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

Meet CKB

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

Cancer Knowledgebase CKB BOOST Demo: Delivering Precision Insights in Oncology

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See how CKB BOOST supports interpretation of complex cancer genomic profiles using expertly curated therapeutic evidence and clinical trial data.

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What you’ll see in this demo
·      Up-to-date, expertly curated therapeutic evidence and clinical trial data
·      How cancer genomic evidence is structured and organized within the platform
·      Advanced search and platform features available exclusively in CKB BOOST

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Complete the form below to view the CKB BOOST demo:

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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
The Most Comprehensive Source of Curated Genomic Evidence + Scientific Experts

We help provide insights into key genetic drivers of diseases and relevant biomarkers. By working together to understand this data, we enable scientists and researchers to make more informed decisions on programs of interest. To learn more about how we can partner together to find your genomic variant solutions, we invite you to click on the link below.

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