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| license: mit | |
| task_categories: | |
| - other | |
| tags: | |
| - spatial-transcriptomics | |
| - xenium | |
| - spatial-omics | |
| - bioinformatics | |
| pretty_name: DeepSpaceDB Xenium Preview | |
| # DeepSpaceDB Xenium Preview | |
| A collection of processed 10x Genomics Xenium spatial transcriptomics samples, curated from public GEO | |
| depositions, stored as [SpatialData](https://spatialdata.scverse.org/) zarr stores. | |
| **This is a small preview** of the full DeepSpaceDB Xenium collection: 3 human breast cancer samples | |
| (DSIDX00001-DSIDX00003, GEO series GSE243168), each provided as an unfiltered `data/` zarr and an analysis-ready `processed/` zarr (see below). `metadata.csv` lists only these samples. | |
| ## Structure | |
| ``` | |
| metadata.csv # one row per sample: organ, condition, species, source, quality, etc. | |
| data/ | |
| DSIDX00001.zarr.zip # one zipped SpatialData zarr store per sample (unfiltered) | |
| ... | |
| processed/ | |
| DSIDX00001.processed.zarr.zip # same samples, filtered / normalized / clustered / annotated | |
| ... | |
| ``` | |
| Each `<id>.zarr.zip` (and `<id>.processed.zarr.zip`) is a [SpatialData](https://spatialdata.scverse.org/) store containing (where available): | |
| - `images`: `morphology_focus` (DAPI/nuclear stain) and `he_image` (H&E, aligned via an `Affine` | |
| transform to the same coordinate space as the other elements) | |
| - `labels`: `cell_labels`, `nucleus_labels` (raster segmentation masks) | |
| - `shapes`: `cell_boundaries`, `nucleus_boundaries`, `cell_circles` | |
| - `points`: `transcripts` (per-molecule detections) | |
| - `tables`: `table` (cell x gene raw count matrix, AnnData) | |
| ## `data/` vs `processed/` | |
| Both folders hold the same samples as SpatialData zarr stores with the same images, labels, shapes and | |
| transcripts. They differ in the `tables/table` AnnData (cell x gene table): | |
| | | `data/` | `processed/` | | |
| |---|---|---| | |
| | Cells | all cells from the Xenium output (DSIDX00001: 167,780) | after cell-level QC filtering (DSIDX00001: 164,000) | | |
| | Expression | raw counts in `X` only | `X` plus `layers`: `counts`, `normalized`, `log1p` | | |
| | Embeddings / graph | none | `obsm`: `X_pca`, `X_umap`; `varm`: `PCs`; `obsp`: `connectivities`, `distances` | | |
| | Clustering | none | `obs.leiden` (Leiden clusters), `obs.banksy_domain` (BANKSY spatial domains) | | |
| | Cell types | none | `obs.predicted_cell_type`, `obs.main_cell_type`, `obs.cell_type_correlation` | | |
| | Per-cell QC | Xenium metrics only | adds `n_counts`, `n_genes_by_counts`, `log1p_n_genes_by_counts`, `log1p_total_counts`, `x`, `y` | | |
| | Per-gene stats | none | `var`: `mean_counts`, `log1p_mean_counts`, `total_counts`, `log1p_total_counts`, `n_cells`, `n_cells_by_counts`, `pct_dropout_by_counts` | | |
| | `uns` | `spatialdata_attrs` | adds `leiden`, `log1p`, `pca`, `umap` | | |
| So `data/` is the minimal, unfiltered Xenium output converted to SpatialData, and `processed/` is the | |
| analysis-ready version: filtered, normalized, embedded, clustered and annotated. Cell types are | |
| assigned per Leiden cluster (by correlation to a reference), so all cells in a cluster share one label. | |
| `morphology_mip` is omitted from both. Files are named `processed/<id>.processed.zarr.zip` and load | |
| exactly like `data/` (extract the zip, then `sd.read_zarr`). | |
| ## Loading a sample | |
| `spatialdata.read_zarr()` cannot currently read directly from a `.zip` (this is an open upstream | |
| limitation - see [scverse/spatialdata#1141](https://github.com/scverse/spatialdata/pull/1141)) - extract | |
| first, then read normally: | |
| ```python | |
| import zipfile | |
| import spatialdata as sd | |
| zipfile.ZipFile("DSIDX00001.zarr.zip").extractall("DSIDX00001.zarr") | |
| sdata = sd.read_zarr("DSIDX00001.zarr") | |
| ``` | |
| ## Selecting samples by metadata | |
| `metadata.csv` lets you filter before downloading any zarr data: | |
| ```python | |
| import pandas as pd | |
| from huggingface_hub import hf_hub_download | |
| meta = pd.read_csv(hf_hub_download(repo_id="vhoncharuk/DeepSpaceDB-Preview", repo_type="dataset", filename="metadata.csv")) | |
| breast_samples = meta[meta.organ == "breast"] | |
| for dsidx_id in breast_samples["id"]: | |
| hf_hub_download(repo_id="vhoncharuk/DeepSpaceDB-Preview", repo_type="dataset", filename=f"data/{dsidx_id}.zarr.zip") | |
| ``` | |
| ## Metadata columns | |
| `id` (internal accession), `sample_id` (GEO GSM or source sample name), `series_id` (GEO GSE, or | |
| source collection), `organism`, `condition` / `condition_detailed` (+ Disease Ontology IDs), `organ` / | |
| `organ_detailed` (+ UBERON IDs), `sex`, `age_or_stage`, `ethnicity_or_strain`, `description`, `source`, | |
| `URL`, `PMID`, `date_published`, `has_manual_annotation`, `platform`, `quality`. | |