The dataset viewer is not available for this split.
Error code: StreamingRowsError
Exception: CastError
Message: Couldn't cast
meta: struct<n_total_cells: int64, n_shown: int64, genome: string, condition: list<item: string>, treg_mod (... 546 chars omitted)
child 0, n_total_cells: int64
child 1, n_shown: int64
child 2, genome: string
child 3, condition: list<item: string>
child 0, item: string
child 4, treg_module_genes: list<item: string>
child 0, item: string
child 5, embedding: string
child 6, cluster_method: string
child 7, clusters: list<item: struct<id: int64, pct: double, program_scores_within_dataset_z: struct<naive_like: double (... 189 chars omitted)
child 0, item: struct<id: int64, pct: double, program_scores_within_dataset_z: struct<naive_like: double, activated (... 177 chars omitted)
child 0, id: int64
child 1, pct: double
child 2, program_scores_within_dataset_z: struct<naive_like: double, activated: double, cycling: double, adhesion_high: double, treg_like: dou (... 4 chars omitted)
child 0, naive_like: double
child 1, activated: double
child 2, cycling: double
child 3, adhesion_high: double
child 4, treg_like: double
child 3, dominant_program_for_display_only: string
child 4, dominant_condition: string
child 5, display_markers: list<item: string>
child 0, item: string
child 8, nomen_ref: string
child 9, emitted_at: string
child 10, title: string
child 11, source_name: string
child 12, source_url: st
...
ore: double
child 4, cluster: int64
child 5, low_conf: bool
child 6, condition: string
child 7, donor: string
child 8, func_margin: double
child 9, th1_like_score: double
child 10, th2_like_score: double
child 11, th17_like_score: double
child 12, tfh_like_score: double
child 13, treg_like_score: double
child 14, cd4_ctl_like_score: double
child 15, th9_like_score: double
child 16, cd4_ctl_like_score_actadj: double
child 17, diff_naive_score: double
child 18, diff_activated_score: double
child 19, diff_memory_score: double
child 20, diff_checkpoint_score: double
child 21, dominant_program_for_display_only: string
reproducibility: struct<seed: int64, pythonhashseed: int64, canonical_table_sha256: string, barcode_set_sha256: strin (... 2 chars omitted)
child 0, seed: int64
child 1, pythonhashseed: int64
child 2, canonical_table_sha256: string
child 3, barcode_set_sha256: string
supersedes: string
outputs: struct<stage01_umap_seed.json: struct<n_cells: int64, content: string>>
child 0, stage01_umap_seed.json: struct<n_cells: int64, content: string>
child 0, n_cells: int64
child 1, content: string
method_version: string
code: string
disclaimer: string
inputs: struct<ntc_clustered.h5ad: struct<sha256: string, subset: string>>
child 0, ntc_clustered.h5ad: struct<sha256: string, subset: string>
child 0, sha256: string
child 1, subset: string
to
{'method_version': Value('string'), 'supersedes': Value('string'), 'inputs': {'ntc_clustered.h5ad': {'sha256': Value('string'), 'subset': Value('string')}}, 'outputs': {'stage01_umap_seed.json': {'n_cells': Value('int64'), 'content': Value('string')}}, 'reproducibility': {'seed': Value('int64'), 'pythonhashseed': Value('int64'), 'canonical_table_sha256': Value('string'), 'barcode_set_sha256': Value('string')}, 'disclaimer': Value('string'), 'code': Value('string')}
because column names don't match
Traceback: Traceback (most recent call last):
File "/src/services/worker/src/worker/utils.py", line 147, in get_rows_or_raise
return get_rows(
dataset=dataset,
...<4 lines>...
column_names=column_names,
)
File "/src/libs/libcommon/src/libcommon/utils.py", line 272, in decorator
return func(*args, **kwargs)
File "/src/services/worker/src/worker/utils.py", line 127, in get_rows
rows_plus_one = list(itertools.islice(safe_iter(ds, dataset=dataset), rows_max_number + 1))
File "/src/services/worker/src/worker/utils.py", line 478, in safe_iter
yield from ds.decode(False) if ds.features else ds
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2818, in __iter__
for key, example in ex_iterable:
^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2355, in __iter__
for key, pa_table in self._iter_arrow():
~~~~~~~~~~~~~~~~^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2380, in _iter_arrow
for key, pa_table in 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/json/json.py", line 343, in _generate_tables
self._cast_table(pa_table, json_field_paths=json_field_paths),
~~~~~~~~~~~~~~~~^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/packaged_modules/json/json.py", line 132, in _cast_table
pa_table = table_cast(pa_table, self.info.features.arrow_schema)
File "/usr/local/lib/python3.14/site-packages/datasets/table.py", line 2369, in table_cast
return cast_table_to_schema(table, schema)
File "/usr/local/lib/python3.14/site-packages/datasets/table.py", line 2297, in cast_table_to_schema
raise CastError(
...<3 lines>...
)
datasets.table.CastError: Couldn't cast
meta: struct<n_total_cells: int64, n_shown: int64, genome: string, condition: list<item: string>, treg_mod (... 546 chars omitted)
child 0, n_total_cells: int64
child 1, n_shown: int64
child 2, genome: string
child 3, condition: list<item: string>
child 0, item: string
child 4, treg_module_genes: list<item: string>
child 0, item: string
child 5, embedding: string
child 6, cluster_method: string
child 7, clusters: list<item: struct<id: int64, pct: double, program_scores_within_dataset_z: struct<naive_like: double (... 189 chars omitted)
child 0, item: struct<id: int64, pct: double, program_scores_within_dataset_z: struct<naive_like: double, activated (... 177 chars omitted)
child 0, id: int64
child 1, pct: double
child 2, program_scores_within_dataset_z: struct<naive_like: double, activated: double, cycling: double, adhesion_high: double, treg_like: dou (... 4 chars omitted)
child 0, naive_like: double
child 1, activated: double
child 2, cycling: double
child 3, adhesion_high: double
child 4, treg_like: double
child 3, dominant_program_for_display_only: string
child 4, dominant_condition: string
child 5, display_markers: list<item: string>
child 0, item: string
child 8, nomen_ref: string
child 9, emitted_at: string
child 10, title: string
child 11, source_name: string
child 12, source_url: st
...
ore: double
child 4, cluster: int64
child 5, low_conf: bool
child 6, condition: string
child 7, donor: string
child 8, func_margin: double
child 9, th1_like_score: double
child 10, th2_like_score: double
child 11, th17_like_score: double
child 12, tfh_like_score: double
child 13, treg_like_score: double
child 14, cd4_ctl_like_score: double
child 15, th9_like_score: double
child 16, cd4_ctl_like_score_actadj: double
child 17, diff_naive_score: double
child 18, diff_activated_score: double
child 19, diff_memory_score: double
child 20, diff_checkpoint_score: double
child 21, dominant_program_for_display_only: string
reproducibility: struct<seed: int64, pythonhashseed: int64, canonical_table_sha256: string, barcode_set_sha256: strin (... 2 chars omitted)
child 0, seed: int64
child 1, pythonhashseed: int64
child 2, canonical_table_sha256: string
child 3, barcode_set_sha256: string
supersedes: string
outputs: struct<stage01_umap_seed.json: struct<n_cells: int64, content: string>>
child 0, stage01_umap_seed.json: struct<n_cells: int64, content: string>
child 0, n_cells: int64
child 1, content: string
method_version: string
code: string
disclaimer: string
inputs: struct<ntc_clustered.h5ad: struct<sha256: string, subset: string>>
child 0, ntc_clustered.h5ad: struct<sha256: string, subset: string>
child 0, sha256: string
child 1, subset: string
to
{'method_version': Value('string'), 'supersedes': Value('string'), 'inputs': {'ntc_clustered.h5ad': {'sha256': Value('string'), 'subset': Value('string')}}, 'outputs': {'stage01_umap_seed.json': {'n_cells': Value('int64'), 'content': Value('string')}}, 'reproducibility': {'seed': Value('int64'), 'pythonhashseed': Value('int64'), 'canonical_table_sha256': Value('string'), 'barcode_set_sha256': Value('string')}, 'disclaimer': Value('string'), 'code': Value('string')}
because column names don't matchNeed help to make the dataset viewer work? Make sure to review how to configure the dataset viewer, and open a discussion for direct support.
spot Stage 1 — CD4 continuous transcriptional-program scores
This repository contains the public data release for spot Stage 1,
method version stage1-continuous-v3.0.1. It provides continuous RNA-program
scores for a quota-balanced non-targeting-control (NTC) subset of the Marson
GWCD4i primary-human-CD4 Perturb-seq dataset.
The scores are measurements of specified transcriptional modules. They are not categorical cell-type, lineage, protein, cytotoxicity, or suppressive-function calls. The Stage-1 scoring and validation outputs contain no inferential p-values, q-values, or FDR estimates and do not report cell-type prevalence.
This dataset repository deliberately contains Stage 1 only. Stage 2–4 result artifacts use additional sources and are not bundled here.
Source and subset
Upstream public source:
- Primary Human CD4+ T Cell Perturb-seq, CZI Virtual Cells Platform, v1.0, released 22 December 2025: https://virtualcellmodels.cziscience.com/dataset/genome-scale-tcell-perturb-seq
- Zhu, Dann, et al., Genome-scale perturb-seq in primary human CD4+ T cells maps context-specific regulators of T cell programs and human immune traits, bioRxiv 2025.12.23.696273, https://doi.org/10.64898/2025.12.23.696273.
- Authors' analysis repository: https://github.com/emdann/GWT_perturbseq_analysis_2025.
ntc_clustered.h5ad is a spot-derived pinned input object, not an original
authors' release file. It contains 396,000 NTC cells: 33,000 cells from each of
four coded donors in each of Rest, Stim8hr, and Stim48hr. This equal quota
is a spot sampling decision and does not preserve the source population's
condition proportions.
The object is 396,000 × 18,130. Its .X matrix is already normalized to a
per-cell target total of approximately 9,819 and log1p transformed. No raw
counts layer is retained. Cluster metadata are retained, but latent and UMAP
matrices are not stored in the H5AD (obsm, obsp, layers, and uns are
empty). Frozen display coordinates are supplied separately.
Scoring method
For cell c and program p:
score(c, p) = mean(.X[c, measured panel genes])
- mean(.X[c, frozen expression-matched control genes])
The deterministic control construction is fully materialized in the release:
- 25 expression bins computed over the pinned 396,000-cell matrix;
- eligible pool = detected genes minus every program marker and activation predictor marker;
- program-order-invariant keyed SHA-256 selection;
- 50 controls per occupied marker bin, without replacement;
- master seed
12345.
There are 11 primary axes: Th1-like, Th2-like, Th17-like, Tfh-like, Treg-like, CD4 CTL-like, Th9-like, Naive, Activated, Memory, and Checkpoint. The activation-adjusted CD4 CTL-like residual is a sensitivity/display lane and is not a primary pole.
Marker panels are curated canonical-marker panels with per-gene primary-source provenance in the registry. Masopust et al., https://doi.org/10.1038/s41577-025-01238-2, is used as a nomenclature framework, not as the source of the marker panels.
Files
| Path | Purpose |
|---|---|
ntc_clustered.h5ad |
Pinned 396,000-cell normalized NTC scoring source object. |
stage1-continuous-v3.0.1/data/stage01_scores_full.parquet |
Authoritative 396,000 × 15 table: barcode, donor, condition, 11 primary scores, and one activation-adjusted sensitivity score. |
stage1-continuous-v3.0.1/data/stage01_summary_v3.json |
Full-table program summaries by condition. |
stage1-continuous-v3.0.1/data/stage01_umap_coordinates.json |
Frozen coordinates for the 40,000-cell display sample. |
stage1-continuous-v3.0.1/data/stage01_umap_overlay_v3_hf.json |
The same 40,000 barcodes with v3 scores; display-only. |
stage1-continuous-v3.0.1/method/ |
Input identity, registry and marker provenance, frozen bins, controls, eligible pool, activation-association diagnostic, and Stage-2 scorer projection. |
stage1-continuous-v3.0.1/validation/ |
Frozen gate specification, descriptive validation, semantic amendment, constituent evidence, and non-gating diagnostics. |
stage1-continuous-v3.0.1/contracts/ |
Generic Stage-1 selection-contract schema. |
stage1-continuous-v3.0.1/receipts/ |
Independent reconstruction receipt. |
MANIFEST.json |
Exact size and SHA-256 ledger for every current release file. |
stage01_stage2_registry_view.json is only a Stage-1 scorer projection for
downstream binding; it is not a Stage-2 result.
Validation status
- Full-score raw SHA-256:
de63b496e8121c77babe380e0c3b5ddfd66f9ce67d0d4e80f55645d177e27e5f. - Canonical full-score content SHA-256:
43c4296d5166740c334441a69df23bb440a073382bbe79628a3bb89e43d51316. - The independent reconstruction receipt reports all checks passing, including exact overlay-to-full score equality for all 40,000 display barcodes.
- The 40,000-cell overlay is not the scientific analysis universe. An archived representativeness diagnostic contains one failed overlay-distribution check; use the full 396,000-cell table for analysis and summaries.
- The frozen validation archive records that 0/33 program-condition pairs
cleared its prospective small-panel leave-one-marker robustness gate. That
result is retained for auditability, has
active_gate:falsein the current selection contract, and is not a claim that the programs are biologically invalid. Null/PENDING selectability fields inside the scorer registry are the pre-validation snapshot;stage01_selectability_v3.jsonrecords the later historical disposition. stage01_activation_association_v1.jsonreports descriptive activation association for every primary axis and the pooled activation-adjusted CTL residual. Activation/timepoint association is not claimed to be removed.
External-dataset confirmation and protein, lineage, and functional validation remain separate biological work; they are not implied by this scoring release.
The HF overlay differs from the repository-generated overlay only in its
top-level explanatory note. Cell records, coordinates, score fields, canonical
score hash, and coordinate hash are unchanged. Both source and emitted raw hashes
are recorded in MANIFEST.json; raw-byte reproduction is not claimed for that
note-only packaging transform.
Reproducibility
The pinned input identity is:
- source HF revision:
e5fcf98b56a9302921d402e97fc5a190bd88f9a6; ntc_clustered.h5adraw SHA-256:2edc6d318415c8b0ee779d707ab86e26ddb6f0274db51ab4a12f21ebfda50e43.
Reproduction and verification code is in the public
spot repository.
The input manifest, control algorithm, materialized controls/bins, validation
constituents, and independent receipt are included here so the release can be
audited without relying on moving branch names.
Privacy
The H5AD contains coded donor, guide, lane, and library identifiers but no donor demographics. In particular, it does not include age, sex, ethnicity, weight, height, smoking status, blood type, or collection date. Coded identifiers may be joinable to upstream public metadata and therefore should not be described as anonymous. Release files were scanned for machine-local paths and credentials.
License and release history
The official CZI dataset page declares the upstream dataset MIT License. The
exact upstream copyright-holder notice is not supplied on that page, so this
repository does not invent one. Spot-authored transformations and metadata are
MIT licensed; see LICENSE and NOTICE.
The historical v2 release is preserved at immutable commit
e5fcf98b56a9302921d402e97fc5a190bd88f9a6 and release tag
stage1-continuous-v2. Its root stage01_umap_seed.json is intentionally absent
from the current tree. v3.0.1 supersedes the earlier categorical-call,
permutation-FDR, prevalence, paper-exact-embedding, and CP10k-equivalence claims;
none of those claims is made by this release.
Current release tag: stage1-continuous-v3.0.1.
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