Who we serve…
What we do…
MASTERMIND GENOMIC SEARCH ENGINE
Search the full text of genomic publications for any gene, variant or keyword for faster, more comprehensive variant interpretation
PRE-CURATED GENOMIC DATASETS FOR PHARMA
Uncover molecular drivers of your disease pathway for drug development and clinical trials with a comprehensive genomic landscape
Automate your variant interpretation workflow with advanced APIs
via a direct connection to Mastermind
Mastermind provides clinically prioritized genomic searches across millions of scientific articles.
Full Text Indexing
Unlike PubMed which only searches titles and abstracts, Mastermind searches the full text of the entire corpus of genomic literature.
Full text sentence matches for genes, variants, and keywords give you deep insight into each article.
Mastermind simple search interface finds any article for any gene or variant you search.
Highlighted Article Content
Quickly narrow your search by the number of times a gene or variant is found in each article.
Workflow automation for gene and variant curation is a snap with the Mastermind API.
I can say with certainty that without the findings obtained from Genomenon, I would not have been able to provide a diagnosis for this patient.
Genomenon’s methodology improved the efficiency and completeness of our literature review process.
We are world-renowned for the speed of our WGS interpretations, and using Mastermind has been a crucial step in accelerating our progress.
I don’t consider a patient’s report complete unless every variant has been researched through Mastermind
We are able to cast a wider net and pick up the most clinically relevant articles with the full text search capabilities of Mastermind.
We looked for the best tools to accelerate literature curation and found there is no comparable solution in the market like Mastermind
Mastermind is the most exhaustive genomic knowledge base in existence, built by indexing nearly seven million full-text genomic articles and 500,000 supplemental data sets.
(Searching Mastermind by phenotype) will be invaluable in our ongoing work to diagnose and treat babies with rare diseases.