Developed at JohnsHopkins, a platform to annotate and prioritize variants and genes in cancer and germline sequencing projects!
🧬 Curious about your genome?
Join our free webinar on OpenCRAVAT to explore and annotate your own data!
📅 July 10 – 1 PM EDT
🎙️ Baker & Karchin (JHU)
🔗 https://tinyurl.com/3ur6vv35
#Genomics #Bioinformatics #OpenScience
#annotator #opencravat #bioinformatics #opensource #webinar #genomes 🖥🧪
🧬 We Want Your Feedback! 🧬
Do you use variant annotation software? We’re gathering insights from the genomics community to improve OpenCRAVAT and understand what features matter most to you.
💡 Take this quick survey (it takes less than 2 minutes!): https://shorturl.at/iOvMt
📌 Your input will help shape better tools for researchers, clinicians, and data scientists.
📸 Scan the QR code below to participate!
🔁 Share with colleagues who use variant annotation tools!
Day 12: “On the twelfth day of OpenCRAVAT, my discovery gave to me…”
🎉 A Genomic Variant Community
Our community is at the heart of everything we do. From researchers to clinicians, your feedback shapes OpenCRAVAT's future. Join us in celebrating our shared journey in variant annotation.
💬 Connect: https://github.com/KarchinLab/open-cravat/discussions
Thank you for being part of our adventure!
⚙️ Day 11: Widgets That Work for You!
Customization is 🔑! OpenCRAVAT’s widgets allow you to visualize variant data in a way that makes sense for your workflow.
🌐 Explore widgets: https://docs.opencravat.org/en/latest/1.-Installation-Instructions.html#installing-viewer-widgets
What’s your favorite widget? Let us know!
