list_sequences
Discover available reference sequences (chromosomes/contigs) in a variant set to obtain valid reference_name values for region-filtered variant searches and QC/diversity analyses.
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) -- copy the exact string from list_variant_sets / list_content, never assemble one by hand: the middle segment is a numeric project index, not the project's name, and a wrong guess fails with an opaque HTTP 500 rather than a clear error. |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| result | Yes |