Get CNV analysis in Mastermind
Discover copy number variants using Mastermind’s Genomic Search Engine –
Start your free trial of Professional Edition today
Start your free trial of Professional Edition today
Mastermind Genomic Search Engine
FASTEST
Find all relevant articles for your specific search criteria, covering every gene, variant, copy number variation (CNV), disease, phenotype, therapy, and categorical keyword.
SMARTEST
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.
MOST COMPREHENSIVE
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
HOW DOES MASTERMIND COMPARE?
A Side-by-Side Summary
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.
| Mastermind | HGMD | ClinVar | |
|---|---|---|---|
| Genes | 19,346 | 15,493 | 17,213 |
| Variants | 23,705,021 | over 456,000 | 1,818,971 |
| Germline Variants | YES | YES | YES |
| Somatic Variants | YES | NO | YES |
| Journals | 36,305 | 3,100 | 3,792 |
| Full-Text Articles Indexed | 9,342,310 | 72,987 | 108,063 |
| Supplemental Datasets Indexed | 3,182,337 | N/A | N/A |
| Update Schedule | Weekly | Quarterly | Weekly |
| Free Version Content | Up to Date | 3 Years Old | Up to Date |
| Interpretation Criteria | ACMG/AMP | Own Criteria | ACMG/AMP |
| ACMG Gene Curation Parameters | YES | NO | NO |
| Clinical Exome Genes Curated based on ClinGen recommendations | YES | NO | NO |
Sources:
http://www.hgmd.cf.ac.uk/ac/stats.php
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429360/
https://www.oncokb.org/
https://cancer.sanger.ac.uk/cosmic/curation
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323903/
https://www.ncbi.nlm.nih.gov/clinvar/submitters/
ftp://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/
https://www.qiagenbioinformatics.com/products/human-gene-mutation-database/1673-2/