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/differential_expression.py
#!/usr/bin/env python3
"""
Differential expression analysis using scvi-tools models.
Uses the trained model's differential_expression method which accounts
for batch effects and uses the generative model for inference.
Usage:
python differential_expression.py model_dir/ adata.h5ad output.csv --groupby leiden
python differential_expression.py model_dir/ adata.h5ad output.csv --groupby cell_type --group1 "T cells" --group2 "B cells"
"""
import argparse
import os
import sys
def run_de_analysis(
model,
adata,
groupby,
group1=None,
group2=None,
n_genes=None
):
"""
Run differential expression analysis.
Parameters
----------
model : scvi model
Trained model with differential_expression method
adata : AnnData
Data used for training
groupby : str
Column in obs to group by
group1 : str, optional
First group (if None, computes for all groups)
group2 : str, optional
Second group (rest if None)
n_genes : int, optional
Limit to top N genes per group
Returns
-------
DataFrame with DE results
"""
import pandas as pd
if group1 is not None:
# Specific comparison
print(f"Comparing {group1} vs {group2 or 'rest'}...")
de_results = model.differential_expression(
groupby=groupby,
group1=group1,
group2=group2
)
# Add comparison info
de_results["comparison"] = f"{group1}_vs_{group2 or 'rest'}"
else:
# All pairwise or one-vs-rest
groups = adata.obs[groupby].unique()
print(f"Computing DE for {len(groups)} groups...")
all_results = []
for group in groups:
print(f" Processing {group}...")
try:
de = model.differential_expression(
groupby=groupby,
group1=group
)
de["group"] = group
all_results.append(de)
except Exception as e:
print(f" Warning: Failed for {group}: {e}")
de_results = pd.concat(all_results, ignore_index=False)
# Filter to significant
if "is_de_fdr_0.05" in de_results.columns:
n_sig = de_results["is_de_fdr_0.05"].sum()
print(f"Found {n_sig} significant DE genes (FDR < 0.05)")
# Limit to top genes if requested
if n_genes is not None and "lfc_mean" in de_results.columns:
if "group" in de_results.columns:
# Top N per group
de_results = de_results.groupby("group").apply(
lambda x: x.nlargest(n_genes, "lfc_mean")
).reset_index(drop=True)
else:
de_results = de_results.nlargest(n_genes, "lfc_mean")
return de_results
def plot_volcano(de_results, output_path, group_name=None):
"""Create volcano plot of DE results."""
import matplotlib.pyplot as plt
import numpy as np
if "lfc_mean" not in de_results.columns:
print("Cannot create volcano plot: missing lfc_mean column")
return
fig, ax = plt.subplots(figsize=(8, 6))
# Get values
lfc = de_results["lfc_mean"].values
if "bayes_factor" in de_results.columns:
y_val = de_results["bayes_factor"].values
y_label = "Bayes Factor"
elif "proba_de" in de_results.columns:
y_val = -np.log10(1 - de_results["proba_de"].values + 1e-10)
y_label = "-log10(1 - P(DE))"
else:
y_val = np.ones(len(lfc))
y_label = ""
# Color by significance
if "is_de_fdr_0.05" in de_results.columns:
sig = de_results["is_de_fdr_0.05"].values
colors = ["red" if s else "gray" for s in sig]
else:
colors = "gray"
ax.scatter(lfc, y_val, c=colors, alpha=0.5, s=10)
ax.axvline(0, color="black", linestyle="--", alpha=0.5)
ax.set_xlabel("Log Fold Change")
ax.set_ylabel(y_label)
title = "Differential Expression"
if group_name:
title += f": {group_name}"
ax.set_title(title)
plt.tight_layout()
plt.savefig(output_path, dpi=150, bbox_inches="tight")
plt.close()
print(f"Volcano plot saved to {output_path}")
def main():
parser = argparse.ArgumentParser(
description="Differential expression with scvi-tools",
formatter_class=argparse.RawDescriptionHelpFormatter,
epilog="""
Examples:
# DE for all clusters (one-vs-rest)
python differential_expression.py model/ adata.h5ad de_results.csv --groupby leiden
# Specific comparison
python differential_expression.py model/ adata.h5ad de_results.csv \\
--groupby cell_type --group1 "T cells" --group2 "B cells"
# Top 50 genes per cluster
python differential_expression.py model/ adata.h5ad de_results.csv \\
--groupby leiden --n-genes 50
"""
)
parser.add_argument("model_dir", help="Directory containing saved model")
parser.add_argument("input", help="Input h5ad file (same as training)")
parser.add_argument("output", help="Output CSV file for DE results")
parser.add_argument("--groupby", required=True, help="Column to group by")
parser.add_argument("--group1", help="First group for comparison")
parser.add_argument("--group2", help="Second group (default: rest)")
parser.add_argument("--n-genes", type=int, help="Limit to top N genes per group")
parser.add_argument("--model-type", choices=["scvi", "scanvi", "totalvi"],
default="scvi", help="Model type (default: scvi)")
parser.add_argument("--plot", action="store_true", help="Generate volcano plot")
args = parser.parse_args()
try:
import scvi
import scanpy as sc
except ImportError:
print("Error: scvi-tools and scanpy required")
sys.exit(1)
# Load data
print(f"Loading {args.input}...")
adata = sc.read_h5ad(args.input)
# Load model
print(f"Loading model from {args.model_dir}...")
if args.model_type == "scvi":
model = scvi.model.SCVI.load(args.model_dir, adata=adata)
elif args.model_type == "scanvi":
model = scvi.model.SCANVI.load(args.model_dir, adata=adata)
elif args.model_type == "totalvi":
model = scvi.model.TOTALVI.load(args.model_dir, adata=adata)
# Run DE
de_results = run_de_analysis(
model,
adata,
groupby=args.groupby,
group1=args.group1,
group2=args.group2,
n_genes=args.n_genes
)
# Save results
de_results.to_csv(args.output)
print(f"DE results saved to {args.output}")
# Plot
if args.plot:
plot_path = args.output.replace(".csv", "_volcano.png")
plot_volcano(de_results, plot_path, args.group1)
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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- Instructions that use the network
- 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