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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
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.
A comprehensive, alphabetical list of the databases available to Franklin University users through the library. 154 Databases found. Academic Search Complete. Index, abstracts, and full text for many scholarly publications covering all academic areas of study. ACM Digital Library.
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.
Highlighted Pages. Watch Franklin Exclusive Webinars. How Franklin is organized. Who was Franklin? Franklin's Advanced Filtering System.
Franklin for WGS solution is an end-to-end suite of tools that help you sharpen single and family case analysis by combining AI technology with the richest genetic data available for simple SNPs and complex variants such as CNVs, ROHs, mitochondrial, and even short tandem repeats.
