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scvi-tools

scvi-tools

github.com/crazymsnData & databases2336 installsUpdated 22w ago
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About scvi-tools

scvi-tools is a Python framework for probabilistic modeling of single-cell genomics data, aimed at researchers analyzing varied assay modalities. Its unified model interface supports deep generative analysis, batch integration, and uncertainty-aware statistical tasks across these data types.

Key features

  1. 01Model single-cell RNA-seq data
  2. 02Analyze chromatin accessibility data
  3. 03Integrate multimodal and multi-omics data
  4. 04Analyze spatial transcriptomics
  5. 05Perform differential expression analysis
  6. 06Annotate cell types and transfer labels

Use cases

  1. 01Correct batches across single-cell studies
  2. 02Integrate paired or unpaired multi-omics
  3. 03Map cell types in spatial data
  4. 04Detect RNA velocity or doublets

Install

Copy the command and run it in a terminal.

$npx skills add https://github.com/crazymsn/academic-skills --skill scvi-tools

After installing, type/scvi-toolsin Claude Code to confirm it loaded.

Bundled files

References and scripts installed along with SKILL.md.

references/
differential-expression.md
models-atac-seq.md
models-multimodal.md
models-scrna-seq.md
models-spatial.md
models-specialized.md
theoretical-foundations.md
workflows.md

Details

From the project README

scvi-tools

Overview

scvi-tools is a comprehensive Python framework for probabilistic models in single-cell genomics. Built on PyTorch and PyTorch Lightning, it provides deep generative models using variational inference for analyzing diverse single-cell data modalities.

When to Use This Skill

Use this skill when:

  • Analyzing single-cell RNA-seq data (dimensionality reduction, batch correction, integration)
  • Working with single-cell ATAC-seq or chromatin accessibility data
  • Integrating multimodal data (CITE-seq, multiome, paired/unpaired datasets)
  • Analyzing spatial transcriptomics data (deconvolution, spatial mapping)
  • Performing differential expression analysis on single-cell data
  • Conducting cell type annotation or transfer learning tasks
  • Working with specialized single-cell modalities (methylation, cytometry, RNA velocity)
  • Building custom probabilistic models for single-cell analysis

Core Capabilities

scvi-tools provides models organized by data modality:

1. Single-Cell RNA-seq Analysis

Core models for expression analysis, batch correction, and integration. See references/models-scrna-seq.md for:

  • scVI: Unsupervised dimensionality reduction and batch correction
  • scANVI: Semi-supervised cell type annotation and integration
  • AUTOZI: Zero-inflation detection and modeling
  • VeloVI: RNA velocity analysis
  • contrastiveVI: Perturbation effect isolation
2. Chromatin Accessibility (ATAC-seq)

Models for analyzing single-cell chromatin data. See references/models-atac-seq.md for:

  • PeakVI: Peak-based ATAC-seq analysis and integration
  • PoissonVI: Quantitative fragment count modeling
  • scBasset: Deep learning approach with motif analysis
3. Multimodal & Multi-omics Integration

Joint analysis of multiple data types. See references/models-multimodal.md for:

  • totalVI: CITE-seq protein and RNA joint modeling
  • MultiVI: Paired and unpaired multi-omic integration
  • MrVI: Multi-resolution cross-sample analysis
4. Spatial Transcriptomics

Spatially-resolved transcriptomics analysis. See references/models-spatial.md for:

  • DestVI: Multi-resolution spatial deconvolution
  • Stereoscope: Cell type deconvolution
  • Tangram: Spatial mapping and integration
  • scVIVA: Cell-environment relationship analysis
5. Specialized Modalities

Additional specialized analysis tools. See references/models-specialized.md for:

  • MethylVI/MethylANVI: Single-cell methylation analysis
  • CytoVI: Flow/mass cytometry batch correction
  • Solo: Doublet detection
  • CellAssign: Marker-based cell type annotation

Typical Workflow

All scvi-tools models follow a consistent API pattern:

# 1. Load and preprocess data (AnnData format)
import scvi
import scanpy as sc

adata = scvi.data.heart_cell_atlas_subsampled()
sc.pp.filter_genes(adata, min_counts=3)
sc.pp.highly_variable_genes(adata, n_top_genes=1200)

# 2. Register data with model (specify layers, covariates)
scvi.model.SCVI.setup_anndata(
    adata,
    layer="counts",  # Use raw counts, not log-normalized
    batch_key="batch",
    categorical_covariate_keys=["donor"],
    continuous_covariate_keys=["percent_mito"]
)

# 3. Create and train model
model = scvi.model.SCVI(adata)
model.train()

# 4. Extract latent representations and normalized values
latent = model.get_latent_representation()
normalized = model.get_normalized_expression(library_size=1e4)

# 5. Store in AnnData for downstream analysis
adata.obsm["X_scVI"] = latent
adata.layers["scvi_normalized"] = normalized

# 6. Downstream analysis with scanpy
sc.pp.neighbors(adata, use_rep="X_scVI")
sc.tl.umap(adata)
sc.tl.leiden(adata)

Key Design Principles:

  • Raw counts required: Models expect unnormalized count data for optimal performance
  • Unified API: Consistent interface across all models (setup → train → extract)
  • AnnData-centric: Seamless integration with the scanpy ecosystem
  • GPU acceleration: Automatic utilization of available GPUs
  • Batch correction: Handle technical variation through covariate registration

Common Analysis Tasks

Differential Expression

Probabilistic DE analysis using the learned generative models:

de_results = model.differential_expression(
    groupby="cell_type",
    group1="TypeA",
    group2="TypeB",
    mode="change",  # Use composite hypothesis testing
    delta=0.25      # Minimum effect size threshold
)

See references/differential-expression.md for detailed methodology and interpretation.

Model Persistence

Save and load trained models:

# Save model
model.save("./model_directory", overwrite=True)

# Load model
model = scvi.model.SCVI.load("./model_directory", adata=adata)
Batch Correction and Integration

Integrate datasets across batches or studies:

# Register batch information
scvi.model.SCVI.setup_anndata(adata, batch_key="study")

# Model automatically learns batch-corrected representations
model = scvi.model.SCVI(adata)
model.train()
latent = model.get_latent_representation()  # Batch-corrected

Theoretical Foundations

scvi-tools is built on:

  • Variational inference: Approximate posterior distributions for scalable Bayesian inference
  • Deep generative models: VAE architectures that learn complex data distributions
  • Amortized inference: Shared neural networks for efficient learning across cells
  • Probabilistic modeling: Principled uncertainty quantification and statistical testing

See references/theoretical-foundations.md for detailed background on the mathematical framework.

Additional Resources

Installation

uv pip install scvi-tools
# For GPU support
uv pip install scvi-tools[cuda]

Best Practices

  1. Use raw counts: Always provide unnormalized count data to models
  2. Filter genes: Remove low-count genes before analysis (e.g., min_counts=3)
  3. Register covariates: Include known technical factors (batch, donor, etc.) in setup_anndata
  4. Feature selection: Use highly variable genes for improved performance
  5. Model saving: Always save trained models to avoid retraining
  6. GPU usage: Enable GPU acceleration for large datasets (accelerator="gpu")
  7. Scanpy integration: Store outputs in AnnData objects for downstream analysis

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