analyze_cnv
Identify copy number variations in spatial transcriptomics data by comparing test cells to reference cell types, revealing chromosomal alterations in tissue.
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 | ||
| warnings | No | Non-fatal conditions that may affect result interpretation. | |
| cnv_score_key | No | ||
| n_chromosomes | Yes | ||
| reference_key | Yes | ||
| n_genes_analyzed | Yes | ||
| reference_categories | Yes | ||
| visualization_available | No |