★ 592 · Updated 2026-10-08
Access gene-drug interactions, clinical guidelines, allele functions, variants, annotations, drug labels, and pharmacogenomic pathways.
Browse skills that share this tag.
★ 592 · Updated 2026-10-08
Access gene-drug interactions, clinical guidelines, allele functions, variants, annotations, drug labels, and pharmacogenomic pathways.
★ 31,836 · Updated 2026-10-06
Query the NHGRI-EBI GWAS Catalog for SNP-trait associations, variants, study metadata, p-values, and summary statistics.
★ 1 · Updated 2026-09-19
Query gene annotations, sequences, variants, orthologs, VEP predictions, and assembly mappings across 250+ species via Ensembl REST API.
★ 399 · Updated 2026-06-15
Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences for NGS pipelines
★ 14 · Updated 2026-06-15
Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences for NGS data
★ 0 · Updated 2026-03-25
Build reusable components using Surface primitives, CVA variants, and design tokens