--- name: scvi-tools description: > Probabilistic single-cell RNA-seq with scvi-tools — scVI for a batch-corrected latent space, scANVI for semi-supervised label transfer, and Bayesian differential expression. Reach for this skill to integrate scRNA-seq batches, embed cells for clustering, transfer annotations from a reference onto a query, or score differentially expressed genes per cluster. For spatial deconvolution / mapping use the cell2location, DestVI, or Tangram methods instead. license: Apache-2.0 requirements: [gpu] metadata: display-name: scvi-tools --- # scvi-tools — scVI / scANVI scvi-tools (Gayoso et al. 2022, github.com/scverse/scvi-tools, BSD-3-Clause) wraps a family of deep generative models for single-cell omics. The scRNA-seq core is **scVI** (unsupervised batch-corrected latent embedding) and **scANVI** (scVI + a classifier head for semi-supervised cell-type label transfer). Both expect **raw integer UMI counts** and emit a low-dimensional `X_scVI` / `X_scANVI` that drops into the scanpy neighbors → leiden → umap pipeline. ## How to run ### scVI — batch-corrected latent space ```python import scanpy as sc import scvi adata = sc.read_h5ad("dataset.h5ad") adata.layers["counts"] = adata.X.copy() # preserve raw BEFORE any normalize/log1p sc.pp.normalize_total(adata); sc.pp.log1p(adata) # optional, for HVG / plotting only sc.pp.highly_variable_genes(adata, n_top_genes=2000, batch_key="batch", subset=True) scvi.model.SCVI.setup_anndata(adata, layer="counts", batch_key="batch") model = scvi.model.SCVI(adata, n_latent=30) model.train(max_epochs=200, early_stopping=True, accelerator="gpu", devices=1) adata.obsm["X_scVI"] = model.get_latent_representation() adata.layers["scvi_normalized"] = model.get_normalized_expression(library_size=1e4) ``` ### scANVI — label transfer from a partially-annotated reference ```python lvae = scvi.model.SCANVI.from_scvi_model( model, labels_key="cell_type", unlabeled_category="Unknown", ) lvae.train(max_epochs=20, n_samples_per_label=100, accelerator="gpu", devices=1) adata.obsm["X_scANVI"] = lvae.get_latent_representation() adata.obs["pred_cell_type"] = lvae.predict() ``` `accelerator="gpu", devices=1` is the PyTorch-Lightning spelling; the legacy `use_gpu=` kwarg was **removed** in scvi-tools 1.x and now raises `TypeError`. ## Differential expression ```python de = model.differential_expression( groupby="leiden", group1="3", # group2=None → vs. all other cells mode="change", delta=0.25, ) top = de.sort_values("proba_de", ascending=False).head(50) ``` For one-vs-rest leave `group2` out — `"rest"` is scanpy's `rank_genes_groups` convention, not scvi-tools'; here `group2` is a literal category name and `"rest"` would match zero cells. scvi-tools ≥1.4 defaults to `mode="vanilla"`, whose result columns are exactly: ``` ['proba_m1', 'proba_m2', 'bayes_factor', 'scale1', 'scale2', 'raw_mean1', 'raw_mean2', 'non_zeros_proportion1', 'non_zeros_proportion2', 'raw_normalized_mean1', 'raw_normalized_mean2', 'comparison', 'group1', 'group2'] ``` — no `lfc_*`, no `proba_de`, no `is_de_fdr_*`. **Pass `mode="change"`** to get `lfc_mean` / `lfc_median` / `proba_de` / `is_de_fdr_0.05`. Sort on `proba_de` (or on `bayes_factor` if you deliberately stayed in vanilla mode). ## Output format | Key | What | | ------------------------------ | ------------------------------------------------------ | | `adata.obsm["X_scVI"]` | `n_cells × n_latent` batch-corrected embedding | | `adata.obsm["X_scANVI"]` | label-aware embedding (better separates known classes) | | `adata.obs["pred_cell_type"]` | scANVI predicted label per cell | | `adata.layers["scvi_normalized"]` | decoded expression, library-size normalized | | DE dataframe | per-gene `lfc_*` / `proba_de` (with `mode="change"`) | ## Remote compute A100-class GPU recommended for >50k cells. The prebuilt **`singlecell_gpu`** Modal env ships scvi-tools 1.4.2 + scanpy 1.11.5 + anndata 0.11.4 — read `compute_details({provider: 'byoc:modal', mode: 'read'})` for the current image ref, then: ```python c = host.compute.create('byoc:modal', provider_params={'modal': { 'image': '', # e.g. im-... 'gpu': 'A100', 'cpu': 8, 'memory': 32768, 'timeout': 3600, }}) job = c.submit_job( intent="scVI+scANVI on 80k cells — 1×A100, ~15 min", inputs=[ {"src": "dataset.h5ad", "dst_filename": "dataset.h5ad"}, {"src": "pipeline.py", "dst_filename": "pipeline.py"}, ], command="python pipeline.py", outputs=["out/**"], timeout_seconds=2400, ) print(job.job_id) # cell ends here — kernel never blocks on compute ``` `h5ad_safe_obs` is auto-loaded into the **local** analysis kernel only — in `pipeline.py` running on Modal, paste the helper at the top of the script (or inline the `pd.Index(np.asarray(..., dtype=object))` coercion) before `.write_h5ad()`. Then call the `wait_for_notification` brain-tool. When `compute_done` arrives, `save_artifacts(payload["featured_files"])`. For the full result dict, re-enter the kernel and bind the **compute handle** (not the job) separately — `.close()` lives on the handle, not on the job: ```python h = host.compute.create('byoc:modal') res = h.attach_job(job_id).result() # output_files, remote_workdir, ... h.close() ``` See the `remote-compute-modal` skill for orchestration details. ## Gotchas | Gotcha | What happens / fix | |---|---| | `differential_expression()` defaults to `mode="vanilla"` (scvi-tools ≥1.4) | `KeyError: 'lfc_mean'` / `'proba_de'` when sorting — pass `mode="change"` to get `lfc_*`/`proba_de`/`is_de_fdr_*`; in vanilla mode sort on `bayes_factor`. | | `adata.obs` index/columns are `string[pyarrow]` (`ArrowStringArray`) | `.write_h5ad()` dies with `IORegistryError: No method registered for writing ` (anndata #2377). Coerce before writing: `adata.obs = h5ad_safe_obs(adata.obs)` (kernel helper — local kernel only; inline the coercion in remote `pipeline.py`). **`.astype(str)` alone is not enough** — on a pyarrow-backed Index/Series it returns another Arrow-backed array; round-trip through `np.asarray(..., dtype=object)`. `anndata.settings.allow_write_nullable_strings = True` does **not** cover Arrow-backed strings. | | `use_gpu=` kwarg | Removed in 1.x → `TypeError: train() got an unexpected keyword argument 'use_gpu'`. Use `accelerator="gpu", devices=1`. | | Log-normalized data fed to `setup_anndata` | Silent garbage — scVI's NB likelihood needs raw integer counts. Stash counts in `adata.layers["counts"]` *before* normalize/log1p and pass `layer="counts"`. | ## Troubleshooting | Symptom | Fix | |---|---| | `KeyError: 'lfc_mean'` (or `'proba_de'`, `'is_de_fdr_0.05'`) on DE result | Add `mode="change"` to `differential_expression()`; the default vanilla mode has no LFC columns. | | `IORegistryError: No method registered for writing ` on `.write_h5ad()` | `adata.obs = h5ad_safe_obs(adata.obs)` (and `adata.var` if needed) before writing. The `allow_write_nullable_strings` flag does not help here. | | `TypeError: ... unexpected keyword argument 'use_gpu'` | Replace with `accelerator="gpu", devices=1`. | | `ValueError: ... non-negative integers` / NB loss explodes | `layer="counts"` points at log/float data — restore raw counts. | | `MisconfigurationException: No supported gpu backend found` | No CUDA visible — drop `accelerator`/`devices` to fall back to CPU, or dispatch via Remote compute. | | `UnicodeEncodeError: 'ascii' codec can't encode character ...` writing a summary / printing | Container has no `LANG` so Python defaults to ASCII. Open files with `encoding="utf-8"` and/or `sys.stdout.reconfigure(encoding="utf-8")` at script top. The prebuilt `singlecell_gpu` env sets `PYTHONIOENCODING=utf-8`, so this only bites user-built images. | | `AttributeError: ... object has no attribute 'close'` on a job handle | You chained `host.compute.create(...).attach_job(...)` and called `.close()` on the job. Bind the compute handle separately and close that — see Remote compute above. | --- **Next**: cluster on `X_scVI` with scanpy (`sc.pp.neighbors(use_rep="X_scVI")` → `sc.tl.leiden` → `sc.tl.umap`); for spatial deconvolution train cell2location / DestVI / Tangram on the scRNA-seq reference.