Enhanced rare disease research.
Accelerate your rare disease research with Mastermind for genomics professionals.
Find all relevant articles for your specific search criteria, covering every gene, variant, copy number variation (CNV), disease, phenotype, therapy, and categorical keyword.
Updated weekly, you can find hidden data and prioritize your results with intelligent tools that bring the most relevant articles to the top for review.
Search beyond title and abstract into the complete text of every published genomic paper, including supplemental data.
Plans to fit your needs.
Gain immediate insight into millions of full text scientific articles with Mastermind. Whether you’re an academic, or part of a global genetics lab, we’ve got solutions for everyone.
MASTERMIND BASIC EDITION
Ideal for students and always free. Start with a complimentary trial of Mastermind Professional Edition. No credit card required and we’ll email the details to get started.
MASTERMIND PROFESSIONAL EDITION
Dive deeper into the published genomic literature with enhanced features including ACMG/AMP classification, supplemental datasets, CNVs, creating alerts and more.
Mastermind Explores Genomic Associations
Users can find, connect, explore, and understand the links between genomic concepts of interest in Mastermind’s intuitive literature search interface.
Identify every Genomic Association in the medical evidence
Draw informative connections between genomic concepts
Find the most data on rare disease genes and variants
In just 3 years, Mastermind surpassed the two primary sources of genomic literature, and we continue to add new data weekly! Here is a snapshot comparison.
|Full-Text Articles Indexed||8,904,722||72,987||95,007|
|Supplemental Datasets Indexed||3,090,690||N/A||N/A|
|Free Version Content||Up to Date||3 Years Old||Up to Date|
|Interpretation Criteria||ACMG/AMP||Own Criteria||ACMG/AMP|