--- tags: - biology - genomics - single-cell-rna-seq task_categories: - text-classification license: cc-by-4.0 --- # Virtual Cell — Patient Example Dataset A minimal sample dataset for verifying the data format and running quick end-to-end checks with [ConvergeBio/virtual-cell-patient](https://huggingface.co/ConvergeBio/virtual-cell-patient). > **This dataset is not intended for training or evaluation.** It contains a > small number of patients and is not representative of a real distribution. > Metrics produced from this dataset should not be interpreted. ## Dataset contents Derived from a public type 1 diabetes scRNA-seq study ([GSE148073](https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE148073)). Preprocessed into the model's input format as a minimal working example. | Split | Patients | Rows | |---|---|---| | train | 8 | 40 | | validation | 3 | 15 | Each row is one augmented view of a patient (5 augmentations per patient). ## Loading ```python from datasets import load_dataset ds = load_dataset("ConvergeBio/virtual-cell-patient-example") train_ds = ds["train"] val_ds = ds["validation"] ``` ## Schema | Column | Shape | Type | Description | |---|---|---|---| | `input_ids` | [500, 18301] | float32 | Log-normalized gene expression matrix, aligned to `gene_names.txt` | | `attention_mask` | [500] | bool | Cell mask (all ones for fixed cell count) | | `labels` | scalar | int | Class index | | `entity_id` | scalar | int | Patient identifier — groups augmented views of the same patient | | `sample_id` | scalar | str | Original sample accession ID | ## Preparing your own dataset ### Input format Each patient is a single `.h5ad` (AnnData) file: ``` adata.X — cell × gene expression matrix (float32, log-normalized) adata.obs — cell-level metadata (cell_type optional) adata.var — gene metadata (index must be HGNC gene symbols) ``` Values should be library-size normalized (target sum 10,000) and `log1p` transformed. The gene axis must be aligned to the 18,301 genes in `gene_names.txt` (from the model repo) — missing genes are zero-filled, extra genes are dropped. ### Quality control (optional) Recommended filters before building the dataset: | Parameter | Default | Description | |---|---|---| | min genes per cell | 200 | Remove low-complexity cells | | max genes per cell | 5,000 | Remove likely doublets | | max mitochondrial % | 10% | Remove dying cells | ### Building the HuggingFace dataset For each patient, randomly sample 500 cells into a `[500, 18301]` float32 matrix. Repeat this sampling independently multiple times per patient to create augmented views — each view becomes a separate row with the same `entity_id`. **Augmentation is strongly encouraged.** The model aggregates predictions across views at inference time, producing more robust results. A factor of 5 augmentations per patient is a good default; 1 is supported but not recommended. Assign each patient a unique integer `entity_id`. All augmented views of the same patient must share the same `entity_id`. The final dataset should be saved in HuggingFace Datasets format: ```python from datasets import DatasetDict dd = DatasetDict({"train": train_ds, "validation": val_ds}) dd.save_to_disk("my_dataset") # or push directly: dd.push_to_hub("my-org/my-dataset") ``` ## Citation If you use this dataset, please cite the original study: ```bibtex @article{sachs2022singlecell, author = {Fasolino, Maria and others}, title = {Single-cell multi-omics analysis of human pancreatic islets reveals novel cellular states in type 1 diabetes}, journal = {Nature Metabolism}, year = {2022}, doi = {10.1038/s42255-022-00531-x}, note = {GEO accession: GSE148073}, } ``` If you use the Virtual Cell patient model, please also cite: ```bibtex @article{convergecell2026, author = {ConvergeBio}, title = {ConvergeCELL: An end-to-end platform from patient transcriptomics to therapeutic hypotheses}, year = {2026}, note = {Preprint available on bioRxiv}, } ``` ## License [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/deed.en)