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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
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Franklin is a network of genomic professionals who share and access real-world evidence data to answer genomic questions and improve patient care. Franklin is powered by Genoox, a platform that connects clinicians, genetic counselors, and healthcare organizations with AI-based variant interpretation and insights.
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
Genoox is a data platform that uses real-world evidence and community input to create genomic insights for clinical decision-making. Franklin is the world’s first open genomic community for professionals, where users can share and access data across the genomic value chain.
Franklin is a platform that uses artificial intelligence to analyze and interpret variant data in case analysis. It integrates evidence from various sources, such as databases, literature, and community data, to prioritize and classify variants according to ACMG/AMP guidelines.
Franklin is a suite of tools that helps you process and interpret whole genome sequencing data from SNPs to complex variants. It uses AI technology, comprehensive databases, and customizable reports to streamline your genome case analysis.
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Learn how to use Franklin, a genomic data analysis platform by Genoox, for various applications and scenarios. Find articles, videos, FAQs, and webinars on Franklin features, functions, and updates.