# Scvi Tools

> 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.

- Skill: `pku-yuangroup/scvi-tools` (Agent Skill, multi-file: 4 files)
- Install (CLI): `npx skillmds@latest add pku-yuangroup/scvi-tools`
- Raw SKILL.md: https://api.skillmd.com/api/skills/pku-yuangroup/scvi-tools/raw
- Safety review: pending
- Works with: Claude Code, Claude.ai, OpenAI Codex
- Category: Coding & Dev Tools
- License: Apache-2.0
- Author: pku-yuangroup (https://skillmd.com/u/pku-yuangroup)
- Updated: 2026-09-17
- Page: https://skillmd.com/skills/pku-yuangroup/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`**
NVIDIA NIM env ships scvi-tools 1.4.2 + scanpy 1.11.5 + anndata 0.11.4 — read
`compute_details({provider: 'byoc:nvidia', mode: 'read'})` for the current
image ref, then:

```python
c = host.compute.create('byoc:nvidia', provider_params={'nvidia': {
    'image': '<image ref from compute_details>', # 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 the NVIDIA NIM job, paste the helper at the top of the script
(or inline the `pd.Index(np.asarray(..., dtype=object))` coercion) before
`.write_h5ad`.

Then poll from a later cell — `.result()` is one non-blocking probe, and it
is what harvests the outputs once the job is terminal; nothing runs in the
background, so a job you never poll is never harvested. Bind the **compute
handle** (not the job) to poll from a fresh kernel — `.close()` lives on the
handle, not on the job:

```python
h = host.compute.create('byoc:nvidia')
res = h.attach_job(job_id).result() # status, output_files, remote_workdir,...
if res["status"] == "succeeded":    # else end the cell and poll again later
    for path in res["featured_files"]:
        host.save_artifact(path)
    h.close()
```

See the `remote-compute-nvidia` 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 <class 'pandas.arrays.ArrowStringArray'>` (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 <class 'pandas.arrays.ArrowStringArray'>` 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.