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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 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 store containing (where available):
images:morphology_focus(DAPI/nuclear stain) andhe_image(H&E, aligned via anAffinetransform to the same coordinate space as the other elements)labels:cell_labels,nucleus_labels(raster segmentation masks)shapes:cell_boundaries,nucleus_boundaries,cell_circlespoints: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) - extract
first, then read normally:
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:
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.