Powering Evidence-Based Genomics


Home of Mastermind
The World’s Most Comprehensive Source of Genomic Evidence

Powering Evidence-Based Genomics

Powering Evidence-Based Genomics


Home of Mastermind
The World’s Most Comprehensive Source of Genomic Evidence

Powering Evidence-Based Genomics

Who we serve…

PHARMA & BIOPHARMA

Optimize drug discovery and clinical trial target selections with acomprehensive genomic landscape for any disease

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CLINICAL DIAGNOSTIC LABS

Accelerate NGS variant interpretation with rapid search and insight into the full text of the genomic literature

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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
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PRE-CURATED GENOMIC DATASETS FOR PHARMA

Uncover molecular drivers of your disease pathway for drug development and clinical trials with a comprehensive genomic landscape
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API AUTOMATION

Automate your variant interpretation workflow with advanced APIs via a direct connection to Mastermind
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Faster Searches

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.

Deep Insight

Full text sentence matches for genes, variants, and keywords give you deep insight into each article.

Comprehensive

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

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.


Lipika Ray, PhD, Rare Genomics Institute
Lipika Ray, PhD, Rare Genomics Institute

Genomenon’s methodology improved the efficiency and completeness of our literature review process.


Alastair Garfield, PhD, Vice President, Translational Research & Development (TRAD), Rhythm Pharmaceuticals
Alastair Garfield, PhD, Vice President, Translational Research & Development (TRAD), Rhythm Pharmaceuticals

We are world-renowned for the speed of our WGS interpretations, and using Mastermind has been a crucial step in accelerating our progress.


Shareef Nahas, Senior Director, Clinical Operations, Rady Children's Institute for Genomic Medicine
Shareef Nahas, Senior Director, Clinical Operations, Rady Children’s Institute for Genomic Medicine

I don’t consider a patient’s report complete unless every variant has been researched through Mastermind


Dr. Nikoletta Sidiropoulos, Medical Director of Genomic Medicine, University of Vermont Health Network
Dr. Nikoletta Sidiropoulos, Medical Director of Genomic Medicine, University of Vermont Health Network

We are able to cast a wider net and pick up the most clinically relevant articles with the full text search capabilities of Mastermind.


Sam Globus, PhD, Director of Scientific Operations, Celmatix
Sam Globus, PhD, Director of Scientific Operations, Celmatix

We looked for the best tools to accelerate literature curation and found there is no comparable solution in the market like Mastermind


James Hirmas, CEO, GenomeNext
James Hirmas, CEO, GenomeNext

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.


Bio-IT World
Bio-IT World

(Searching Mastermind by phenotype) will be invaluable in our ongoing work to diagnose and treat babies with rare diseases.


Shareef Nahas, Senior Director, Clinical Operations, Rady Children's Institute for Genomic Medicine
Shareef Nahas, Senior Director, Clinical Operations, Rady Children’s Institute for Genomic Medicine

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