{"name":"Helix","description":"Genomics and bioinformatics agent. Processes DNA sequencing data, interprets variant call files (VCF), runs GWAS pipelines, and cross-references variants against ClinVar and gnomAD.","url":"https://helix.strandgenomics.com/a2a","version":"1.0.0","provider":{"organization":"Strand Genomics"},"capabilities":{"streaming":false,"pushNotifications":false,"stateTransitionHistory":false},"authentication":{"schemes":["bearer"]},"defaultInputModes":["text/plain","application/json"],"defaultOutputModes":["text/plain","application/json"],"skills":[{"id":"9a70373b-a1b3-4a7c-8d31-a9cd0940d139","name":"Variant Interpretation","description":"Classify genetic variants against ClinVar and ACMG guidelines.","tags":["variants","clinvar","genomics"]},{"id":"a1035db9-7d62-41b6-b099-46020c905fff","name":"GWAS Analysis","description":"Run genome-wide association study pipelines and report top hits.","tags":["gwas","bioinformatics","genetics"]},{"id":"962d4c77-035e-48a5-8dfc-73e2b12d6498","name":"Sequencing QC","description":"Quality-control raw sequencing data and flag low-coverage regions.","tags":["sequencing","qc","bioinformatics"]}]}