The dataset viewer is not available for this split.
Error code: FeaturesError
Exception: ParserError
Message: Error tokenizing data. C error: Expected 21 fields in line 3, saw 27
Traceback: Traceback (most recent call last):
File "/src/services/worker/src/worker/job_runners/split/first_rows.py", line 243, in compute_first_rows_from_streaming_response
iterable_dataset = iterable_dataset._resolve_features()
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 4379, in _resolve_features
features = _infer_features_from_batch(self.with_format(None)._head())
~~~~~~~~~~~~~~~~~~~~~~~~~~~~^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2661, in _head
return next(iter(self.iter(batch_size=n)))
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2839, in iter
for key, pa_table in ex_iterable.iter_arrow():
~~~~~~~~~~~~~~~~~~~~~~^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2377, in _iter_arrow
yield from self.ex_iterable._iter_arrow()
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 536, in _iter_arrow
for key, pa_table in iterator:
^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 419, in _iter_arrow
for key, pa_table in self.generate_tables_fn(**gen_kwags):
~~~~~~~~~~~~~~~~~~~~~~~^^^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/packaged_modules/csv/csv.py", line 198, in _generate_tables
for batch_idx, df in enumerate(csv_file_reader):
~~~~~~~~~^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/pandas/io/parsers/readers.py", line 1843, in __next__
return self.get_chunk()
~~~~~~~~~~~~~~^^
File "/usr/local/lib/python3.14/site-packages/pandas/io/parsers/readers.py", line 1985, in get_chunk
return self.read(nrows=size)
~~~~~~~~~^^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/pandas/io/parsers/readers.py", line 1923, in read
) = self._engine.read( # type: ignore[attr-defined]
~~~~~~~~~~~~~~~~~^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
nrows
^^^^^
)
^
File "/usr/local/lib/python3.14/site-packages/pandas/io/parsers/c_parser_wrapper.py", line 234, in read
chunks = self._reader.read_low_memory(nrows)
File "pandas/_libs/parsers.pyx", line 850, in pandas._libs.parsers.TextReader.read_low_memory
File "pandas/_libs/parsers.pyx", line 905, in pandas._libs.parsers.TextReader._read_rows
File "pandas/_libs/parsers.pyx", line 874, in pandas._libs.parsers.TextReader._tokenize_rows
File "pandas/_libs/parsers.pyx", line 891, in pandas._libs.parsers.TextReader._check_tokenize_status
File "pandas/_libs/parsers.pyx", line 2061, in pandas._libs.parsers.raise_parser_error
pandas.errors.ParserError: Error tokenizing data. C error: Expected 21 fields in line 3, saw 27Need help to make the dataset viewer work? Make sure to review how to configure the dataset viewer, and open a discussion for direct support.
MIST Dataset Construction For SPATIA (ICML 2026)
MIST (Multimodal Imaging and Spatial Transcriptomics) is the pretraining dataset. It combines cell-level gene expression with morphology image crops from Xenium spatial transcriptomics data. Construction has three stages:
Stage A: Crop cell images into LMDB
Crop cell-centered patches from Xenium morphology TIFF images and store them in an LMDB database.
Input layout (per Xenium dataset):
dataset_dir/
├── morphology_mip.ome.tif # or morphology.ome.tif / DAPI.tif
├── cells.parquet # cell centroids + boundaries
└── cell_feature_matrix.h5 # (optional, for building h5ad)
Crop pipeline:
cd gene_encoders/SPATIA-scprint
# Standard Xenium format (cells.parquet + morphology.ome.tif)
python scripts/0510_crop_images_cell_refactored.py \
--output-lmdb /path/to/output/dataset_name.lmdb \
--output-size 256 \
--cache /path/to/cache
# SPATCH format (adata.h5ad + DAPI.tif, for COAD/HCC/OV datasets)
python scripts/0510_crop_images_cell_spatch.py \
--input-dir /path/to/SPATCH/Xenium-5K \
--output-lmdb /path/to/output/lmdb \
--dataset-name HCC
Image processing details:
- TIFF max intensity projection across channels
- Normalize to uint8 (0-255)
- Crop around cell centroid (adaptive size from cell boundaries, or default 32px radius)
- Resize to 256x256
- Store as raw bytes in LMDB with key format:
{dataset_name}/{cell_id} - Coordinate mapping:
pixel_x = spatial_y / 0.2125,pixel_y = spatial_x / 0.2125(Xenium coordinate swap)
Stage B: Build annotated h5ad and register in lamindb
Annotate each dataset with ontology metadata and add to a lamindb Collection:
cd gene_encoders/SPATIA-scprint
python scripts/0512_add_single_dataset.py \
/path/to/adata.h5ad \
--tissue lung --disease normal \
--dataset_name xenium_lung \
--collection_name xenium_all_0212
Required metadata columns (added automatically by the script):
organism_ontology_term_id(e.g.,NCBITaxon:9606)cell_type_ontology_term_id,tissue_ontology_term_id,disease_ontology_term_idassay_ontology_term_id,sex_ontology_term_id,development_stage_ontology_term_iddonor_id,dataset_name,index(cell ID matching LMDB keys)
Stage C: Merge per-dataset LMDBs (optional)
Consolidate multiple per-dataset LMDBs into a single file:
python scripts/0514_merge_lmdb.py \
--input-dir /path/to/per_dataset_lmdbs/ \
--output /path/to/merged/all.lmdb
Data loading at training time
The training data loader (scdataloader.data_spatial.Dataset) reads:
- Gene expression from a lamindb Collection (multiple h5ad files)
- Cell images from LMDB files (supports multiple scales)
LMDB environments are mapped to image keys in the batch:
- 1st LMDB path ->
image(cell-level crop) - 2nd LMDB path ->
region_image(niche-level, optional) - 3rd LMDB path ->
tissue_image(tissue-level, optional)
Images are preprocessed at load time: 256x256 grayscale -> stack to RGB ->
AutoImageProcessor (ViT-MAE) -> (3, 224, 224) float tensor.
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