Developed at JohnsHopkins, a platform to annotate and prioritize variants and genes in cancer and germline sequencing projects!
Developed at JohnsHopkins, a platform to annotate and prioritize variants and genes in cancer and germline sequencing projects!
Help shape the future of genomic variant annotation! We’re looking for members of the genomics, bioinformatics, and clinical variant interpretation community to help improve OpenCRAVAT. As a community contributor, you could help by: Suggesting or developing new annotators and resources Testing new features Improving documentation and training materials Providing feedback on workflows and usability Sharing OpenCRAVAT in your community Completing this form does not obligate you to contribute — it simply lets us know you’re interested.
🧬 Want to explore your own genome?
Join our free webinar on how to use OpenCRAVAT to annotate & interpret your personal variants.
📅 July 10 | 🕐 1 PM EDT
🎙️ With Jasmine Baker, PhD & Rachel Karchin, PhD
🔗 https://tinyurl.com/3ur6vv35
#Genomics #Bioinformatics #OpenSource #OpenCRAVAT