a web app that can classify how likely specific mutations in DNA are to cause diseases (variant effect prediction). We will deploy and use the state-of-the-art Evo2 large language model, and use it to predict the pathogenicity of single nucleotide variants (SNVs)
What is the GeneralSubhra/variant-analysis-evo2 GitHub project? Description: " a web app that can classify how likely specific mutations in DNA are to cause diseases (variant effect prediction). We will deploy and use the state-of-the-art Evo2 large language model, and use it to predict the pathogenicity of single nucleotide variants (SNVs)". Written in TypeScript. Explain what it does, its main use cases, key features, and who would benefit from using it.
Question is copied to clipboard — paste it after the AI opens.
Clone via HTTPS
Clone via SSH
Download ZIP
Download master.zipReport bugs or request features on the variant-analysis-evo2 issue tracker:
Open GitHub Issues