Integrate comprehensive data into your pipeline
Comprehensive solutions providing insights at the gene and the variant level.
Genomenon Data
Access comprehensive data that includes expertly curated gene and variant-level content with indexed variant-level data.
Utilize to interpret somatic variants and identify the most relevant therapy via efficacy evidence annotations.
Streamline your research workflow with automated evidence collection and real-time updates.
Mastermind FLEX Data
- 9,000 gene-disease relationships across 6,500 genes
- Updated monthly
- Thorough review of external publications, clinical evidence, functional evidence
- Classification and inheritance patterns
- Extensive repository of germline data
- Adheres to ACMG guidelines to facilitate in-depth variant-level analysis
- Access all the necessary information to interpret variants and supporting evidence
Often combined with Curated Gene File
- Highly detailed and sensitive information about genetic variants
- Updated quarterly
- Ensures researchers don't miss crucial information in order to make informed decisions
Cancer Knowledgebase (CKB) FLEX Data
Get the information you need on therapeutic treatments. Easily mine curated content for drugs with clinical and preclinical evidence to gain insights into treatment options and access real-time clinical trial information for oncologists and patients.
You can also view resistance data for targeted therapies to assist with monitoring response, identify clinical areas lacking research evidence, and see the connections to growing data complexity with genomic signatures.
Utilize translational model data to identify the models best suited for research and interrogate clinically actionable genes for gene panel design. With FLEX, users can also interpret data from NGS assays, liquid biopsies, and expression studies, and quickly locate genomic variants with biochemical functional effect.
Indexed Data [API]
The Indexed Data API unlocks article insights, empowering users to:
- Standardize and prioritize variants of interest with ease
- Automate VCF annotation and complex time-based analyses
- Support organizational capabilities, including internal database updates
24,000,000
variants
25,000
genes
15,000
phenotypes
69,000
drug therapies
Standardization, Automation & Variant Prioritization
Automate evidence querying speeding their analyses and enables researchers to only analyze variants of interest.
VUS Reanalysis
Retrieve updated evidence at your cadence intervals and based on specific criteria such as time.
Support Internal Database Updates
Get PMIDs and article metadata after manual curation to support internal databases.
Talk to a Genomenon expert.
