analyze_cnv
Analyze copy number variations (CNVs) in spatial transcriptomics data using a reference cell population to identify genomic alterations.
Instructions
Analyze copy number variations (CNVs) in spatial transcriptomics data.
Args:
data_id: Dataset identifier
params: Required - reference_key, reference_categories, and optional method/thresholds.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| params | Yes | ||
| data_id | Yes |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| method | Yes | ||
| data_id | Yes | ||
| statistics | No | ||
| cnv_score_key | No | ||
| n_chromosomes | Yes | ||
| reference_key | Yes | ||
| n_genes_analyzed | Yes | ||
| reference_categories | Yes | ||
| visualization_available | No |