Install
$ agentstack add skill-shoko-official-claude-science-system-prompts-scvi-tools ✓ scanned · ✓ verified, works with Claude Code, Cursor, and more.
Security review
✓ PassedNo issues found. Passed automated security review. · v0.1.0 How review works →
- ✓ Prompt-injection patterns
- ✓ Secret / credential exfiltration
- ✓ Dangerous shell & filesystem operations
- ✓ Untrusted network calls
- ✓ Known-malicious package signatures
What it can access
- ✓ Network access No
- ✓ Filesystem access No
- ✓ Shell / process execution No
- ✓ Environment & secrets No
- ✓ Dynamic code execution No
From automated source analysis of v0.1.0. “Used” means the capability is present in the source — more access means more to trust, not that it’s unsafe.
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Reliability & compatibility
Declared compatibility
Compatibility is declared by the source manifest. End-to-end runtime verification is coming, see below.
We're building live execution health for every listing: tool-call success rate, median latency, uptime, and last-checked timestamps, measured, not self-reported. It isn't live yet, so we don't show numbers we can't stand behind.
How agent discovery & health will work →About
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
``python adata.layers["counts"] = adata.X.copy() # Before normalization scvi.model.SCVI.setup_anndata(adata, layer="counts") ``
- HVG selection: Use 2000-4000 highly variable genes
``python 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
``python 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
Source & license
This open-source skill is cataloged on AgentStack and links to its original source — we do not rehost the code.
- Author: Shoko-official
- Source: Shoko-official/Claude-Science-System-Prompts
- License: Apache-2.0
Install and usage instructions live in the source repository linked above.
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Versions
- v0.1.0 Imported from the upstream source.