Knowledgebase.
In a world of incredible researchers and clinicians, we’ve created the world’s most clinically robust, intelligent
knowledgebase to connect them.
Fueled by expert content curation, an extensive rules engine, and machine learning, we are here to serve the
most current and diverse clinical genomics data in a way that helps you focus on what matters most, providing
world-class patient care.
Curated to transform precision medicine.
Current Data
With real-time publishing of medical interpretations from our customer-based network of peers and weekly updates to therapy guidelines and clinical trials, our Knowledgebase contains the most up-to-date, clinically actionable information for NGS.
Diverse Data
Content includes curated genomic data, clinical practice guidelines, drug labels, published results of clinical research, and information on clinical trials recruiting closest to your patients.
Relevant Data
The Knowledgebase is built on top of a powerful rules engine that intelligently considers global content and accurately delivers the richest set of rationalized medical interpretations.
A comprehensive approach to sourcing.
With unique relationships to a wide range of data sources, the Velsera Knowledgebase puts a full ecosystem of information at your disposal.
Individual biomarker associations with clinical evidence
- FDA and EMA-approved labels
- NCCN, ASCO, and ESMO guidelines
- PubMed literature
- Active, recruiting trials from clinicaltrials.gov and EUCT
- Clinical evidence synthesized into high-quality, ready-to-use interpretations
Public data sources
- Human genome builds
- Gene-RNA-protein models
- gnomAD
- COSMIC, TCGA, ClinVar, dbNSFP
- PubMed literature search engine
Real-world medical content
- Medically signed-out interpretations and classifications from our Interpretation Services and partner sites
Individual biomarker associations with clinical evidence
- FDA and EMA-approved labels
- NCCN, ASCO, and ESMO guidelines
- PubMed literature
- Active, recruiting trials from clinicaltrials.gov and EUCT
- Clinical evidence synthesized into high-quality, ready-to-use interpretations
Public data sources
- Human genome builds
- Gene-RNA-protein models
- gnomAD
- COSMIC, TCGA, ClinVar, dbNSFP
- PubMed literature search engine
Real-world medical content
- Medically signed-out interpretations and classifications from our Interpretation Services and partner sites