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Franklin - The Future of Variant Interpretation. The most advanced way for variant classification, a FREE comprehensive interpretation tool by Genoox. Try it - search any variant
Franklin allows genomic professionals to spend less time pinpointing evidence, and more time drilling down into insights and actionability. We are building the largest, most diverse real-world evidence dataset – answering any genomic question through the power of the community, data and insights.
Search Our Databases. Databases will assist you in locating needed information to successfully complete your research and assignments. They provide access to reliable, scholarly, historically relevant, and diverse information. You can search for specific databases by name, by major, or by type.
Franklin's Publication engine Explore Franklin's rich and comprehensive genomic literature database for SNP and CNV interpretation. External Sources and Databases. Data sources Updated list of databases and tools integrated into the Franklin platform.
Our indication agnostic data platform delivers accurate insights driven by our community of clinical users, Franklin. The real-world evidence we produce enhances clinical decision-making, fine-tunes care pathways and enables more targeted therapies.
Explore variants data in Franklin. Welcome to Franklin by Genoox! The purpose of this guide is to help you take your first steps using Franklin.
The Library's FRANKLIN database provides access to 2,000 fully-cataloged public domain photographs from the collections of the Roosevelt Library. Additional images will be added to FRANKLIN on an ongoing basis throughout the coming years.
