list_sequences
List the reference sequences (chromosomes/contigs) in a variant set to obtain valid reference names for downstream variant queries and analysis.
Instructions
List the reference sequences (chromosomes/contigs) available in a variant set.
Use this to discover valid reference_name values for the region filters on
count_variants / search_variants / the QC & diversity tools.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| variant_set_db_id | Yes | BrAPI variantSetDbId identifying the run (MODULE§project§run); from list_variant_sets / list_content. |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| result | Yes |