Genomics
Interpret genomic variants with ACMG classification, pharmacogenomics, and clinical annotation from ClinVar and gnomAD.
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Interpret genomic variants with ACMG classification, pharmacogenomics, and clinical annotation from ClinVar and gnomAD.
Annotate VCF variants with Ensembl VEP, ClinVar, and gnomAD. Ranks variants by impact (HIGH/MODERATE/LOW/MODIFIER) and generates a reproducible report.
Annotate VCF variants with Ensembl VEP REST, ClinVar significance, gnomAD/population frequency context, and prioritized
Annotate VCF variants with Ensembl VEP, ClinVar, and gnomAD. Ranks variants by impact (HIGH/MODERATE/LOW/MODIFIER) and generates a reproducible report.
Query gnomAD for variant allele frequency across populations. Uses FAVOR to convert rsID→variant_id first, then queries gnomAD.
Agent skill for Data Analyst, ML / AI Engineer, Researcher, published by openai. Project details and file access are provided by the publisher.
Agent skill for Data Analyst, ML / AI Engineer, Researcher, published by Michaelunkai. Project details and file access are provided by the publisher.
Agent skill for Data Analyst, ML / AI Engineer, Researcher, published by ilderaj. Project details and file access are provided by the publisher.
Agent skill for Data Analyst, ML / AI Engineer, Researcher, published by gaos6e. Project details and file access are provided by the publisher.
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