Comprehensive Genomic Intelligence, Unmatched Insights
Experience faster, more accurate variant interpretation with Genomenon's Mastermind. Built by scientists & clinicians, Mastermind streamlines your workflow, boosts diagnostic yield, and accelerates results - empowering researchers and physicians to find disease-causing genes and deliver better patient care.
Discover how Mastermind can transform your curation and variant interpretation today!
Mastermind Genomic Intelligence Platform
Did you know that PubMed misses about 94% of variant citations?
Variant scientists face significant challenges in accessing detailed variant-level information and meaningfully applying ACMG classifications efficiently and effectively. Genomenon's Mastermind PRO enables you to access:
- Gene disease relationship insights
- Literature support for Copy Number Variants
- Curated content on breast cancer panel, cardiac panels, hereditary cancer panels, ACMG secondary findings & more...
- Insights on more than 27 million variants
We analyze over 10 million full-text articles, 3.7 million supplemental articles, giving you comprehensive, in-depth information to speed up diagnosis and improve outcomes.
Reduce Turnaround Time
Quickly identify and review the genetic evidence, clinically prioritized with insight into each genomic article to speed variant interpretation for rare diseases.
Increase Diagnostic Yield
Access 100X more genomic evidence and 20X more variants than other sources to find relevant genomic articles, resolve more VUSs, and diagnose more patients.
Accelerate Throughput
Optimize your workflows by rapidly prioritizing variants of disease-causing genes, simplifying your analysis and enabling a more targeted approach.
Trusted by 20,000+ Users in 140+ Countries
Why is searching for genomic literature so hard?
Legacy Nomenclature Makes Genomic Evidence Hard to Find
More than 74% of the genomic variants in publications are still in non-normalized forms1, making citations hard to find, even in resources like NCBI’s PubMed.
Data is Hidden in the Body and Supplemental Text of Genomic Articles
Fewer than 6% of variants are identified in the title or abstract in NCBI’s PubMed, the remainder present in the full-text or supplemental files1.
Be ready for Rare Disease Day 2025 and learn how Genomenon can help your search.
