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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.

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

Paper

Estimation of ENPP1 deficiency genetic prevalence using a comprehensive literature review and population databases

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Read the paper here.

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Published in the Orphanet Journal of Rare Diseases, this paper reveals how Mastermind determined the genetic prevalence of ENPP1 deficiency to be 3X the previous estimate.

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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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