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scvi-tools Deep Learning

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Advanced tools for single-cell genomic analysis.

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What scvi-tools Deep Learning does

The scvi-tools skill provides a comprehensive suite of resources for deep learning-based single-cell analysis, specifically designed for users working with single-cell genomics data. This skill is particularly useful for researchers and developers who need to perform tasks such as data integration, batch correction, and multi-modal analysis. By leveraging the capabilities of scvi-tools, users can efficiently analyze complex datasets, including RNA sequencing (scRNA-seq), ATAC-seq, and spatial transcriptomics data.

To utilize this skill, users can follow a structured approach that involves selecting the appropriate workflow based on their data type and analysis needs. The skill offers detailed reference files that guide users through the steps required for each model, ensuring that they can effectively implement deep learning methods without needing to write extensive code from scratch. The provided scripts cover a range of common tasks, from data preparation to model training and evaluation, making it easier to manage single-cell analysis workflows.

With specific models for various data types, such as scVI for unsupervised integration and scANVI for label transfer, users can choose the best approach for their analysis. The skill also supports advanced features like spatial deconvolution with DestVI and RNA velocity analysis with veloVI, allowing for a deeper understanding of cellular dynamics. Overall, scvi-tools is an essential resource for those engaged in single-cell research, providing the tools necessary to extract meaningful insights from complex biological data.

When to use it

Use this skill when you are working with single-cell genomic data and require advanced analysis techniques such as integration, batch correction, or multi-modal analysis.

When not to use it

This skill may not be suitable for users who are not working with single-cell data or do not require deep learning methods for their analysis.

What you can build with it

Integrating scRNA-seq Data

Use scVI or scANVI to integrate multiple scRNA-seq datasets, leveraging batch information for improved analysis.

Analyzing Multi-Modal Data

Employ totalVI for CITE-seq data to analyze RNA and protein simultaneously, enhancing your insights into cellular functions.

Spatial Transcriptomics Analysis

Utilize DestVI for cell type deconvolution in spatial transcriptomics, allowing for a detailed understanding of tissue architecture.

How to install scvi-tools Deep Learning

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1. Install with the skills CLI

npx skills add anthropics/knowledge-work-plugins/scvi-tools --agent claude-code

2. Or install it manually

Download the skill folder and drop it into ~/.claude/skills/ for all projects, or .claude/skills/ to scope it to one repo. Restart Claude Code so it picks up the new skill.

Anthropic's agentic coding CLI, and the reference implementation of Agent Skills. Drop a skill folder into ~/.claude/skills and Claude Code loads it automatically whenever a task matches the skill's description. Claude Code docs

Inside SKILL.md

Written by anthropics

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 TypeModelPrimary Use Case
scRNA-seqscVIUnsupervised integration, DE, imputation
scRNA-seq + labelsscANVILabel transfer, semi-supervised integration
CITE-seq (RNA+protein)totalVIMulti-modal integration, protein denoising
scATAC-seqPeakVIChromatin accessibility analysis
Multiome (RNA+ATAC)MultiVIJoint modality analysis
Spatial + scRNA referenceDestVICell type deconvolution
RNA velocityveloVITranscriptional dynamics
Cross-technologysysVISystem-level batch correction

Workflow Reference Files

WorkflowReference FileDescription
Environment Setupreferences/environment_setup.mdInstallation, GPU, version info
Data Preparationreferences/data_preparation.mdFormatting data for any model
scRNA Integrationreferences/scrna_integration.mdscVI/scANVI batch correction
ATAC-seq Analysisreferences/atac_peakvi.mdPeakVI for accessibility
CITE-seq Analysisreferences/citeseq_totalvi.mdtotalVI for protein+RNA
Multiome Analysisreferences/multiome_multivi.mdMultiVI for RNA+ATAC
Spatial Deconvolutionreferences/spatial_deconvolution.mdDestVI spatial analysis
Label Transferreferences/label_transfer.mdscANVI reference mapping
scArches Mappingreferences/scarches_mapping.mdQuery-to-reference mapping
Batch Correctionreferences/batch_correction_sysvi.mdAdvanced batch methods
RNA Velocityreferences/rna_velocity_velovi.mdveloVI dynamics
Troubleshootingreferences/troubleshooting.mdCommon issues and solutions

CLI Scripts

Modular scripts for common workflows. Chain together or modify as needed.

Pipeline Scripts

ScriptPurposeUsage
prepare_data.pyQC, filter, HVG selectionpython scripts/prepare_data.py raw.h5ad prepared.h5ad --batch-key batch
train_model.pyTrain any scvi-tools modelpython scripts/train_model.py prepared.h5ad results/ --model scvi
cluster_embed.pyNeighbors, UMAP, Leidenpython scripts/cluster_embed.py adata.h5ad results/
differential_expression.pyDE analysispython scripts/differential_expression.py model/ adata.h5ad de.csv --groupby leiden
transfer_labels.pyLabel transfer with scANVIpython scripts/transfer_labels.py ref_model/ query.h5ad results/
integrate_datasets.pyMulti-dataset integrationpython scripts/integrate_datasets.py results/ data1.h5ad data2.h5ad
validate_adata.pyCheck data compatibilitypython 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:

FunctionPurpose
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?
├── 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

Frequently asked questions about scvi-tools Deep Learning

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