OmicVerse built-in datasets: pbmc3k, pancreas, dentategyrus, zebrafish, immune, spatial, multiome, plus create_mock_dataset() and predefined_signatures GMT gene sets.
ov.datasets provides 30+ ready-to-use datasets with automatic download, caching, and fallback to mock data. Use these instead of manually downloading files or relying on scanpy.datasets.
create_mock_dataset() to generate synthetic data without downloadspredefined_signatures for curated GMT gene sets (cell cycle, gender, mitochondrial, tissue-specific)| Function |
|---|
| Cells |
|---|
| Genes |
|---|
| Description |
|---|
ov.datasets.pbmc3k() | 2,700 | 32,738 | 10x PBMC3k (raw or processed) |
ov.datasets.pbmc8k() | ~8,000 | — | 10x PBMC 8k |
ov.datasets.paul15() | 2,730 | 3,451 | Myeloid progenitors |
ov.datasets.krumsiek11() | 640 | 11 | Myeloid differentiation simulation |
ov.datasets.bone_marrow() | 5,780 | 27,876 | Bone marrow hematopoietic |
ov.datasets.hematopoiesis() | — | — | Processed hematopoiesis |
ov.datasets.hematopoiesis_raw() | — | — | Raw hematopoiesis |
ov.datasets.sc_ref_Lymph_Node() | ~10,000 | ~15,000 | Lymph node reference |
ov.datasets.bhattacherjee() | ~5,000 | ~2,000 | Mouse PFC cocaine study |
ov.datasets.human_tfs() | — | — | Human TF list (DataFrame) |
| Function | Cells | Genes | Description |
|---|---|---|---|
ov.datasets.dentate_gyrus() | 18,213 | 27,998 | Dentate gyrus (loom) |
ov.datasets.dentate_gyrus_scvelo() | 2,930 | 13,913 | DG subset from scVelo |
ov.datasets.zebrafish() | 4,181 | 16,940 | Zebrafish developmental |
ov.datasets.pancreatic_endocrinogenesis() | — | — | Pancreatic epithelial |
ov.datasets.pancreas_cellrank() | 2,930 | 13,913 | Pancreas cellrank benchmark |
ov.datasets.scnt_seq_neuron_splicing() | 13,476 | 44,021 | scNT-seq neuron splicing |
ov.datasets.scnt_seq_neuron_labeling() | 3,060 | 24,078 | scNT-seq neuron labeling |
ov.datasets.sceu_seq_rpe1() | ~2,930 | ~13,913 | scEU-seq RPE1 |
ov.datasets.sceu_seq_organoid() | 3,831 | 9,157 | scEU-seq organoid |
ov.datasets.haber() | 7,216 | 27,998 | Intestinal epithelium |
ov.datasets.chromaffin() | — | — | Chromaffin cell lineage |
ov.datasets.hg_forebrain_glutamatergic() | 1,720 | 32,738 | Human forebrain |
ov.datasets.toggleswitch() | 200 | 2 | Two-gene simulation |
| Function | Description |
|---|---|
ov.datasets.seqfish() | SeqFISH spatial transcriptomics |
ov.datasets.multi_brain_5k() | 10x E18 mouse brain multiome (MuData) |
| Function | Description |
|---|---|
ov.datasets.burczynski06() | UC/CD PBMC bulk (127 samples) |
ov.datasets.moignard15() | Embryo hematopoiesis qRT-PCR |
ov.datasets.decov_bulk_covid_bulk() | COVID-19 PBMC bulk |
ov.datasets.decov_bulk_covid_single() | COVID-19 PBMC single-cell ref |
| Function | Description |
|---|---|
ov.datasets.create_mock_dataset() | Configurable synthetic scRNA-seq |
ov.datasets.blobs() | Gaussian blob clusters |
Use create_mock_dataset() when you need data without network access or for pipeline testing:
import omicverse as ov
# Basic mock dataset
adata = ov.datasets.create_mock_dataset(
n_cells=2000,
n_genes=1500,
n_cell_types=6,
with_clustering=False,
random_state=42,
)
# adata.obs: cell_type, sample_id, condition, tissue
# adata.var: gene_symbols, highly_variable
# With full preprocessing (normalized, PCA, UMAP, leiden)
adata = ov.datasets.create_mock_dataset(
n_cells=5000,
n_genes=3000,
n_cell_types=10,
with_clustering=True,
)
Features:
Gene_0001, Gene_0002, ...with_clustering=True adds: normalization, HVG, scaling, PCA, UMAP, leidenPre-loaded GMT files for common scoring tasks:
from omicverse.datasets import predefined_signatures, load_signatures_from_file
# Available signature keys
print(list(predefined_signatures.keys()))
# ['cell_cycle_human', 'cell_cycle_mouse', 'gender_human', 'gender_mouse',
# 'mitochondrial_genes_human', 'mitochondrial_genes_mouse',
# 'ribosomal_genes_human', 'ribosomal_genes_mouse',
# 'apoptosis_human', 'apoptosis_mouse',
# 'human_lung', 'mouse_lung', 'mouse_brain', 'mouse_liver', 'emt_human']
# Load a signature → dict[str, list[str]]
cell_cycle = load_signatures_from_file(predefined_signatures['cell_cycle_human'])
# {'S_genes': ['MCM5', 'PCNA', ...], 'G2M_genes': ['HMGB2', 'CDK1', ...]}
# Use with scoring
import scanpy as sc
sc.tl.score_genes_cell_cycle(adata, s_genes=cell_cycle['S_genes'],
g2m_genes=cell_cycle['G2M_genes'])
# CORRECT: use ov.datasets for standard benchmarks
adata = ov.datasets.pbmc3k()
# WRONG: manually downloading what's already built-in
# import urllib.request
# urllib.request.urlretrieve('https://...', 'pbmc3k.h5ad') # unnecessary!
# adata = ov.read('pbmc3k.h5ad')
# CORRECT: pbmc3k(processed=True) for pre-processed version
adata = ov.datasets.pbmc3k(processed=True)
# WRONG: loading raw then manually preprocessing for a demo
# adata = ov.datasets.pbmc3k()
# sc.pp.normalize_total(adata) # unnecessary if you just need a quick demo
# CORRECT: mock data for testing (no network needed)
adata = ov.datasets.create_mock_dataset(n_cells=500, n_genes=200)
# WRONG: creating synthetic data manually with numpy
# X = np.random.poisson(1, (500, 200)) # missing metadata, layers, etc.
./data/ (relative to working directory)var_names_make_unique() called automatically after loadingdownload_data_requests() with custom headers. If persistent, manually download the file to ./data/ with the expected filename and the function will find it.ModuleNotFoundError: No module named 'muon' when calling multi_brain_5k(): Install muon: pip install muon. This function returns MuData, not AnnData..raw or layers['counts']: Add manually after creation: ov.utils.store_layers(adata, layers='counts') and adata.raw = adata.load_signatures_from_file returns empty dict: Verify the GMT file path. Use predefined_signatures['key'] which resolves to the bundled file via importlib.resources.ov.datasets.dentate_gyrus_scvelo() for the smaller pre-processed subset (2,930 cells).omicverse, scanpy, anndata, numpy, pandastqdm, requests (for mirror fallback)muon (only for multi_brain_5k())importlib.resources (stdlib)reference.md