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The dataset viewer is not available for this split.
Cannot load the dataset split (in streaming mode) to extract the first rows.
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 match

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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:

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:false in 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.json records the later historical disposition.
  • stage01_activation_association_v1.json reports 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.h5ad raw 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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