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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,…
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 code For installation or GPU issues, consult references/environment_setup.md 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 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 scvi-tools Documentation scvi-tools Tutorials Model Hub GitHub Issues
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