Genomenon
Accelerating NGS variant interpretation, this drug discovery software enables rapid exploration of genomic literature, offering insights into over 26 million variants. Researchers can efficiently prioritize variants linked to diseases and therapies, leveraging a robust database and expert curation to streamline analysis and enhance confidence in identifying disease-causing variants, ultimately advancing precision medicine.
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Top Genomenon Features
- Rapid NGS variant interpretation
- Comprehensive genetics view
- Germline and somatic exploration
- 26 million variant articles
- Cancer Knowledgebase integration
- Tailored expert solutions
- Constantly updated genomic database
- Pre-classified variant catalog
- Genomic Intelligence Platform
- Optimized variant prioritization
- Mastermind publication access
- Filterable literature results
- Gene page integration
- Enhanced Evidence page navigation
- AI-driven patient assessments
- Complete genomic data access
- Precision medicine support
- Empirical evidence backing
- Pathogenic variant identification
- Efficient research workflows
