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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.
- My Cases
My Cases - Franklin - Genoox
- Knowledge Base
Knowledge Base - Franklin - Genoox
- Log in to Your Organization
Log in to Your Organization - Franklin - Genoox
- Franklin
Franklin - Franklin - Genoox
- How to Start Using Franklin
Explore variants data in Franklin. Welcome to Franklin by...
- My Cases
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 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.
Genoox is a platform that uses real-world evidence and community data to make genomic data actionable at the point of care. Franklin is the world’s first open genomic community for professionals, created by Genoox.
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.
Franklin is a comprehensive tool for exploring and interpreting variants data in genomic research. Learn how to use Franklin's features, such as collections, filters, annotations, and reports, in this guide.
Franklin is a platform that helps you analyze WES data from SNPs, CNVs, ROHs, and mitochondrial variants. It uses AI, bioinformatic tools, and community knowledge to streamline your case analysis from FASTQ to report.
