Welcome to the 12 Days of OpenCRAVAT! 🎄 Each day, we’ll explore a different feature or tool that makes OpenCRAVAT an essential platform for genomic variant analysis. Whether you’re a seasoned researcher or just beginning your journey, our adventurer’s guide will help you unlock the full potential of OpenCRAVAT.
On Day 1, we’re spotlighting the Single Variant Tool—a quick and powerful feature for annotating one variant at a time. Perfect for small-scale queries or rapid testing, this tool delivers fast, reliable results to help you understand the impact and context of a single variant. It’s intuitive, efficient, and now more accessible than ever through our updated website. Start your analysis today with the Single Variant Tool!
This tool is especially useful for those working on clinical or exploratory research, where rapid answers about variant significance can make a big difference. With just a few clicks, you can uncover detailed information about pathogenicity, population frequency, and more, all presented in an easy-to-read report.
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