Scvi Tools
AnthropicOfficialPublished by Anthropic
- Skill
- Tool integration
- Data and AI
- Apache-2.0
- Low risk
- Has scripts
AutoGineer summary
Written by AutoGineer from the skill’s own files, not by the author
scvi-tools provides a suite of probabilistic models designed for the analysis of single-cell data, including scRNA-seq, scATAC-seq, and multi-modal datasets. It leverages variational autoencoders to handle batch correction, data integration, label transfer, and dimensionality reduction. This skill serves as a guide for utilizing specific models like scVI, scANVI, totalVI, PeakVI, MultiVI, DestVI, and veloVI, offering standardized workflows, CLI scripts for pipeline automation, and best practices for data preparation and model training.
What it does
- Performs batch correction and data integration across different experimental conditions.
- Supports multi-modal analysis for CITE-seq and multiome (RNA+ATAC) data.
- Enables label transfer and reference mapping between query and reference datasets.
- Facilitates spatial transcriptomics deconvolution and RNA velocity estimation.
- Provides modular Python scripts for common analysis pipelines.
- Offers guidance on model selection based on specific data types and research goals.
When to use it
- When integrating multiple single-cell datasets with significant batch effects.
- When analyzing multi-modal data such as CITE-seq or joint RNA+ATAC profiles.
- When performing reference-based label transfer or query-to-reference mapping.
- When conducting deep learning-based dimensionality reduction for clustering and visualization.
- When working with spatial transcriptomics or RNA velocity data.
Advantages
- Standardized approach to complex single-cell deep learning workflows.
- Modular scripts allow for reproducible and scalable analysis pipelines.
- Comprehensive model selection guide for diverse genomic data types.
- Built-in support for advanced tasks like batch correction and multi-modal integration.
- Clear documentation on data preparation requirements for probabilistic models.
Usage examples
- “How do I integrate two scRNA-seq datasets using scVI?”
- The agent provides the workflow for preparing the AnnData objects, selecting highly variable genes, setting up the model with batch keys, and training the scVI model.
- “I have CITE-seq data, which model should I use?”
- The agent identifies totalVI as the appropriate model and directs the user to the corresponding reference file for multi-modal integration.
- “How can I map my new scRNA-seq query data to an existing reference?”
- The agent explains the use of scArches for query-to-reference mapping and provides the necessary steps to configure the model.
- “What are the requirements for input data before training a model?”
- The agent outlines the necessity of raw integer count data, the importance of highly variable gene selection, and how to correctly set up the AnnData object.
Install
Download the skill as a ZIP:
https://mp-staging.autogineer.com/agent-skills/anthropics/scvi-tools/downloadUnzip it into the cross-client skills folder of your project:
mkdir -p .agents/skills && unzip scvi-tools.zip -d .agents/skills
Documentation by Anthropic
scvi-tools Deep Learning Skill
This skill provides guidance for deep learning-based single-cell analysis using scvi-tools, the leading framework for probabilistic models in single-cell genomics.
How to Use This Skill
Identify the appropriate workflow from the model/workflow tables below
Read the corresponding reference file for detailed steps and code
Use scripts in
scripts/to avoid rewriting common codeFor installation or GPU issues, consult
references/environment_setup.mdFor debugging, consult
references/troubleshooting.md
When to Use This Skill
When scvi-tools, scVI, scANVI, or related models are mentioned
When deep learning-based batch correction or integration is needed
When working with multi-modal data (CITE-seq, multiome)
When reference mapping or label transfer is required
When analyzing ATAC-seq or spatial transcriptomics data
When learning latent representations of single-cell data
Model Selection Guide
| Data Type | Model | Primary Use Case |
|---|---|---|
| scRNA-seq | scVI | Unsupervised integration, DE, imputation |
| scRNA-seq + labels | scANVI | Label transfer, semi-supervised integration |
| CITE-seq (RNA+protein) | totalVI | Multi-modal integration, protein denoising |
| scATAC-seq | PeakVI | Chromatin accessibility analysis |
| Multiome (RNA+ATAC) | MultiVI | Joint modality analysis |
| Spatial + scRNA reference | DestVI | Cell type deconvolution |
| RNA velocity | veloVI | Transcriptional dynamics |
| Cross-technology | sysVI | System-level batch correction |
Workflow Reference Files
| Workflow | Reference File | Description |
|---|---|---|
| Environment Setup | references/environment_setup.md | Installation, GPU, version info |
| Data Preparation | references/data_preparation.md | Formatting data for any model |
| scRNA Integration | references/scrna_integration.md | scVI/scANVI batch correction |
| ATAC-seq Analysis | references/atac_peakvi.md | PeakVI for accessibility |
| CITE-seq Analysis | references/citeseq_totalvi.md | totalVI for protein+RNA |
| Multiome Analysis | references/multiome_multivi.md | MultiVI for RNA+ATAC |
| Spatial Deconvolution | references/spatial_deconvolution.md | DestVI spatial analysis |
| Label Transfer | references/label_transfer.md | scANVI reference mapping |
| scArches Mapping | references/scarches_mapping.md | Query-to-reference mapping |
| Batch Correction | references/batch_correction_sysvi.md | Advanced batch methods |
| RNA Velocity | references/rna_velocity_velovi.md | veloVI dynamics |
| Troubleshooting | references/troubleshooting.md | Common issues and solutions |
CLI Scripts
Modular scripts for common workflows. Chain together or modify as needed.
Pipeline Scripts
| Script | Purpose | Usage |
|---|---|---|
prepare_data.py | QC, filter, HVG selection | python scripts/prepare_data.py raw.h5ad prepared.h5ad --batch-key batch |
train_model.py | Train any scvi-tools model | python scripts/train_model.py prepared.h5ad results/ --model scvi |
cluster_embed.py | Neighbors, UMAP, Leiden | python scripts/cluster_embed.py adata.h5ad results/ |
differential_expression.py | DE analysis | python scripts/differential_expression.py model/ adata.h5ad de.csv --groupby leiden |
transfer_labels.py | Label transfer with scANVI | python scripts/transfer_labels.py ref_model/ query.h5ad results/ |
integrate_datasets.py | Multi-dataset integration | python scripts/integrate_datasets.py results/ data1.h5ad data2.h5ad |
validate_adata.py | Check data compatibility | python scripts/validate_adata.py data.h5ad --batch-key batch |
Example Workflow
# 1. Validate input data
python scripts/validate_adata.py raw.h5ad --batch-key batch --suggest
# 2. Prepare data (QC, HVG selection)
python scripts/prepare_data.py raw.h5ad prepared.h5ad --batch-key batch --n-hvgs 2000
# 3. Train model
python scripts/train_model.py prepared.h5ad results/ --model scvi --batch-key batch
# 4. Cluster and visualize
python scripts/cluster_embed.py results/adata_trained.h5ad results/ --resolution 0.8
# 5. Differential expression
python scripts/differential_expression.py results/model results/adata_clustered.h5ad results/de.csv --groupby leidenPython Utilities
The scripts/model_utils.py provides importable functions for custom workflows:
| Function | Purpose |
|---|---|
prepare_adata() | Data preparation (QC, HVG, layer setup) |
train_scvi() | Train scVI or scANVI |
evaluate_integration() | Compute integration metrics |
get_marker_genes() | Extract DE markers |
save_results() | Save model, data, plots |
auto_select_model() | Suggest best model |
quick_clustering() | Neighbors + UMAP + Leiden |
Critical Requirements
Raw counts required: scvi-tools models require integer count data
adata.layers["counts"] = adata.X.copy() # Before normalization scvi.model.SCVI.setup_anndata(adata, layer="counts")HVG selection: Use 2000-4000 highly variable genes
sc.pp.highly_variable_genes(adata, n_top_genes=2000, batch_key="batch", layer="counts", flavor="seurat_v3") adata = adata[:, adata.var['highly_variable']].copy()Batch information: Specify batch_key for integration
scvi.model.SCVI.setup_anndata(adata, layer="counts", batch_key="batch")
Quick Decision Tree
Need to integrate scRNA-seq data?
├── Have cell type labels? → scANVI (references/label_transfer.md)
└── No labels? → scVI (references/scrna_integration.md)
Have multi-modal data?
├── CITE-seq (RNA + protein)? → totalVI (references/citeseq_totalvi.md)
├── Multiome (RNA + ATAC)? → MultiVI (references/multiome_multivi.md)
└── scATAC-seq only? → PeakVI (references/atac_peakvi.md)
Have spatial data?
└── Need cell type deconvolution? → DestVI (references/spatial_deconvolution.md)
Have pre-trained reference model?
└── Map query to reference? → scArches (references/scarches_mapping.md)
Need RNA velocity?
└── veloVI (references/rna_velocity_velovi.md)
Strong cross-technology batch effects?
└── sysVI (references/batch_correction_sysvi.md)Key Resources
Files
- ATTRIBUTION.mdAdded by AutoGineer932 B
- LICENSE.txt10.0 KiB
- SKILL.md7.2 KiB
- references/atac_peakvi.md9.3 KiB
- references/batch_correction_sysvi.md10.2 KiB
- references/citeseq_totalvi.md10.1 KiB
- references/data_preparation.md6.2 KiB
- references/environment_setup.md6.3 KiB
- references/label_transfer.md10.2 KiB
- references/multiome_multivi.md8.9 KiB
- references/rna_velocity_velovi.md8.6 KiB
- references/scarches_mapping.md10.8 KiB
- references/scrna_integration.md9.6 KiB
- references/spatial_deconvolution.md11.2 KiB
- references/troubleshooting.md10.8 KiB
- scripts/cluster_embed.pyScript6.3 KiB
- scripts/differential_expression.pyScript6.7 KiB
- scripts/integrate_datasets.pyScript6.9 KiB
- scripts/model_utils.pyScript17.0 KiB
- scripts/prepare_data.pyScript5.1 KiB
- scripts/train_model.pyScript11.3 KiB
- scripts/transfer_labels.pyScript7.2 KiB
- scripts/validate_adata.pyScript11.9 KiB
scripts/transfer_labels.py
#!/usr/bin/env python3
"""
Transfer cell type labels from reference to query using scANVI.
Maps query cells to a pre-trained reference model and predicts cell types.
Usage:
python transfer_labels.py reference_model/ query.h5ad output_dir/
python transfer_labels.py reference_model/ query.h5ad output_dir/ --confidence 0.7
"""
import argparse
import os
import sys
def transfer_labels(
reference_model,
adata_query,
max_epochs=100,
confidence_threshold=0.5
):
"""
Transfer labels from reference to query.
Parameters
----------
reference_model : SCANVI model
Pre-trained scANVI model
adata_query : AnnData
Query data to annotate
max_epochs : int
Fine-tuning epochs
confidence_threshold : float
Minimum confidence for predictions
Returns
-------
AnnData with predictions
"""
import scvi
import numpy as np
# Get reference genes
ref_genes = reference_model.adata.var_names
print(f"Reference genes: {len(ref_genes)}")
# Check gene overlap
query_genes = adata_query.var_names
common = ref_genes.intersection(query_genes)
print(f"Query genes: {len(query_genes)}")
print(f"Common genes: {len(common)} ({len(common)/len(ref_genes)*100:.1f}%)")
if len(common) < len(ref_genes) * 0.5:
print("Warning: Less than 50% gene overlap. Results may be unreliable.")
# Subset query to reference genes
# Missing genes will be filled with zeros
adata_query = adata_query[:, adata_query.var_names.isin(ref_genes)].copy()
# Ensure counts layer
if "counts" not in adata_query.layers:
adata_query.layers["counts"] = adata_query.X.copy()
# Prepare query for mapping
print("Preparing query data...")
scvi.model.SCANVI.prepare_query_anndata(adata_query, reference_model)
# Create query model
print("Creating query model...")
query_model = scvi.model.SCANVI.load_query_data(
adata_query,
reference_model
)
# Fine-tune
print(f"Fine-tuning ({max_epochs} epochs)...")
query_model.train(
max_epochs=max_epochs,
plan_kwargs={"weight_decay": 0.0}
)
# Get predictions
print("Getting predictions...")
predictions = query_model.predict()
soft_predictions = query_model.predict(soft=True)
adata_query.obs["predicted_cell_type"] = predictions
adata_query.obs["prediction_confidence"] = soft_predictions.max(axis=1)
adata_query.obs["confident_prediction"] = adata_query.obs["prediction_confidence"] >= confidence_threshold
# Get latent representation
adata_query.obsm["X_scANVI"] = query_model.get_latent_representation()
# Stats
n_confident = adata_query.obs["confident_prediction"].sum()
print(f"\nPrediction summary:")
print(f" Total cells: {adata_query.n_obs}")
print(f" Confident (>= {confidence_threshold}): {n_confident} ({n_confident/adata_query.n_obs*100:.1f}%)")
print(f" Mean confidence: {adata_query.obs['prediction_confidence'].mean():.3f}")
print("\nPredicted cell types:")
print(adata_query.obs["predicted_cell_type"].value_counts())
return adata_query, query_model
def plot_predictions(adata, output_dir):
"""Plot prediction results."""
import scanpy as sc
import matplotlib.pyplot as plt
# Compute UMAP if needed
if "X_umap" not in adata.obsm:
sc.pp.neighbors(adata, use_rep="X_scANVI")
sc.tl.umap(adata)
# Plot
fig, axes = plt.subplots(1, 3, figsize=(15, 4))
sc.pl.umap(adata, color="predicted_cell_type", ax=axes[0], show=False,
title="Predicted Cell Type")
sc.pl.umap(adata, color="prediction_confidence", ax=axes[1], show=False,
title="Prediction Confidence", cmap="viridis")
sc.pl.umap(adata, color="confident_prediction", ax=axes[2], show=False,
title="Confident Predictions")
plt.tight_layout()
plot_path = os.path.join(output_dir, "predictions.png")
plt.savefig(plot_path, dpi=150, bbox_inches="tight")
plt.close()
print(f"Prediction plot saved to {plot_path}")
def main():
parser = argparse.ArgumentParser(
description="Transfer cell type labels using scANVI",
formatter_class=argparse.RawDescriptionHelpFormatter,
epilog="""
Examples:
# Basic label transfer
python transfer_labels.py reference_model/ query.h5ad results/
# With confidence threshold
python transfer_labels.py reference_model/ query.h5ad results/ --confidence 0.7
# More fine-tuning
python transfer_labels.py reference_model/ query.h5ad results/ --max-epochs 200
"""
)
parser.add_argument("model_dir", help="Directory containing reference scANVI model")
parser.add_argument("query", help="Query h5ad file to annotate")
parser.add_argument("output_dir", help="Output directory")
parser.add_argument("--reference-adata", help="Reference adata used for training (if not saved with model)")
parser.add_argument("--max-epochs", type=int, default=100,
help="Fine-tuning epochs (default: 100)")
parser.add_argument("--confidence", type=float, default=0.5,
help="Confidence threshold (default: 0.5)")
args = parser.parse_args()
try:
import scvi
import scanpy as sc
except ImportError:
print("Error: scvi-tools and scanpy required")
sys.exit(1)
# Create output directory
os.makedirs(args.output_dir, exist_ok=True)
# Load query data
print(f"Loading query data: {args.query}")
adata_query = sc.read_h5ad(args.query)
print(f"Query: {adata_query.shape}")
# Load reference model
print(f"Loading reference model: {args.model_dir}")
if args.reference_adata:
ref_adata = sc.read_h5ad(args.reference_adata)
reference_model = scvi.model.SCANVI.load(args.model_dir, adata=ref_adata)
else:
# Try loading without adata (works if model was saved with adata)
try:
reference_model = scvi.model.SCANVI.load(args.model_dir)
except ValueError as e:
if "no saved anndata" in str(e).lower():
print("Error: Model was saved without adata. Please provide --reference-adata")
sys.exit(1)
raise
print(f"Reference: {reference_model.adata.shape}")
# Transfer labels
adata_annotated, query_model = transfer_labels(
reference_model,
adata_query,
max_epochs=args.max_epochs,
confidence_threshold=args.confidence
)
# Save results
adata_path = os.path.join(args.output_dir, "query_annotated.h5ad")
adata_annotated.write_h5ad(adata_path)
print(f"\nAnnotated data saved to {adata_path}")
# Save query model
model_path = os.path.join(args.output_dir, "query_model")
query_model.save(model_path)
print(f"Query model saved to {model_path}")
# Save predictions CSV
pred_df = adata_annotated.obs[["predicted_cell_type", "prediction_confidence", "confident_prediction"]]
pred_path = os.path.join(args.output_dir, "predictions.csv")
pred_df.to_csv(pred_path)
print(f"Predictions saved to {pred_path}")
# Plot
plot_predictions(adata_annotated, args.output_dir)
print("\nDone!")
if __name__ == "__main__":
main()
Requirements and compatibility
Written for: Claude Code, Claude apps
Works with: Claude Code, Claude apps, OpenAI Codex, GitHub Copilot, Cursor, Gemini CLI, Kiro, OpenCode, Goose, Amp, Roo Code, JetBrains Junie, Factory Droid, Devin (ex-Windsurf), Mistral Vibe, OpenHands, Letta
“Works with” means the tool reads the open Agent Skills format; a skill written for one tool may use features others lack.
Needs: Needs Python
Security
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- Scripts that your agent may run
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Attribution and licence
- Published by
- Anthropic
- Publisher
- Anthropic (Official)
- Source
- anthropics/knowledge-work-plugins · bio-research/skills/scvi-tools · commit e050c2e
- Licence
- Apache License 2.0 (redistribution allowed)
- ATTRIBUTION.md (written by AutoGineer)
- Synced
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Download ZIP
The ZIP holds the skill’s files, its licence files and an ATTRIBUTION.md. Download scvi-tools.zip