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Deep learning for single-cell analysis using scvi-tools. This skill should be used when users need (1) data integration and batch correction with scVI/scANVI, (2) ATAC-seq analysis with PeakVI, (3) CITE-seq multi-modal analysis with totalVI, (4) multiome RNA+ATAC analysis with MultiVI, (5) spatial transcriptomics deconvolution with DestVI, (6) label transfer and reference mapping with scANVI/scArches, (7) RNA velocity with veloVI, or (8) any deep learning-based single-cell method. Triggers include mentions of scVI, scANVI, totalVI, PeakVI, MultiVI, DestVI, veloVI, sysVI, scArches, variational autoencoder, VAE, batch correction, data integration, multi-modal, CITE-seq, multiome, reference mapping, latent space.

Use this Skill: https://skilld.dev/gh/anthropics/knowledge-work-plugins/scvi-tools

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SKILL.md

โ‰ˆ183 tokens always: the name and description. โ‰ˆ1.7k when used: this file. โ‰ˆ29k more on demand in 12 files.

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

  1. Identify the appropriate workflow from the model/workflow tables below
  2. Read the corresponding reference file for detailed steps and code
  3. Use scripts in scripts/ to avoid rewriting common code
  4. For installation or GPU issues, consult references/environment_setup.md
  5. For 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 leiden

Python 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

  1. 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")
  2. 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()
  3. 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?
โ”œโ”€โ”€ Have cell type labels? โ†’ scANVI (references/label_transfer.md)
โ””โ”€โ”€ No labels? โ†’ scVI (references/scrna_integration.md)

Have multi-modal data?
โ”œโ”€โ”€ CITE-seq (RNA + protein)? โ†’ totalVI (references/citeseq_totalvi.md)
โ”œโ”€โ”€ Multiome (RNA + ATAC)? โ†’ MultiVI (references/multiome_multivi.md)
โ””โ”€โ”€ scATAC-seq only? โ†’ PeakVI (references/atac_peakvi.md)

Have spatial data?
โ””โ”€โ”€ Need cell type deconvolution? โ†’ DestVI (references/spatial_deconvolution.md)

Have pre-trained reference model?
โ””โ”€โ”€ Map query to reference? โ†’ scArches (references/scarches_mapping.md)

Need RNA velocity?
โ””โ”€โ”€ veloVI (references/rna_velocity_velovi.md)

Strong cross-technology batch effects?
โ””โ”€โ”€ sysVI (references/batch_correction_sysvi.md)

Key Resources

Source: SKILL.md on GitHub

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    This skill provides a comprehensive and well-documented toolkit for single-cell genomic analysis using the scvi-tools framework. It includes modular scripts and reference guides for biological data integration, multi-modal analysis, and reference mapping. The skill adheres to standard scientific computing practices, including the use of established package registries and model repositories like Hugging Face for managing environment setup and model assets.

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