On the fourth day of OpenCRAVAT, we’re celebrating the power of trusted annotation sources! Annotation is at the heart of variant interpretation, and OpenCRAVAT integrates some of the most reliable and widely used databases to ensure your results are accurate and comprehensive.
Among the many sources available, four stand out for their unique contributions:
- gnomAD4 provides population frequency data, helping you distinguish between common and rare variants.
- dbSNP catalogs known single nucleotide polymorphisms and indels for quick reference.
- ClinVar offers clinical significance classifications, aiding in the identification of pathogenic variants.
- COSMIC focuses on cancer-related mutations, supporting oncological research and interpretation.
Together, these databases empower you to analyze variants with confidence and clarity. By leveraging the latest curated data, you can uncover insights that drive discovery and decision-making. Whether you’re focusing on rare genetic disorders, cancer genomics, or general research, OpenCRAVAT’s comprehensive annotation sources provide the foundation you need.
Explore these trusted sources today and see how OpenCRAVAT transforms your genomic data into meaningful insights!
👉 [Link to annotator list]
