The dataset viewer is not available for this split.
Error code: StreamingRowsError
Exception: CastError
Message: Couldn't cast
backend: string
coreneuron_gpu: bool
duration_ms: int64
elapsed_seconds: double
exc_gmax_scale: double
generator: struct<backend: string, biophysics_hoc_sha256: string, code_revision: struct<commit: string, dirty: (... 456 chars omitted)
child 0, backend: string
child 1, biophysics_hoc_sha256: string
child 2, code_revision: struct<commit: string, dirty: bool>
child 0, commit: string
child 1, dirty: bool
child 3, data_version: string
child 4, dt_ms: double
child 5, exc_gmax_scale: double
child 6, inh_gmax_scale: double
child 7, input_routing: string
child 8, input_sampler: string
child 9, integrator: string
child 10, mechanism_files: list<item: string>
child 0, item: string
child 11, mechanisms_sha256: string
child 12, morphology_sha256: string
child 13, neuron_version: string
child 14, nseg_policy: string
child 15, soma_samples_per_ms: int64
child 16, spike_label_rule: string
child 17, synapse_delay_ms: double
child 18, synapses: string
child 19, teacher: string
child 20, template_hoc_sha256: string
child 21, v_init_mv: double
inh_gmax_scale: double
input_event_policy: string
input_routing: struct<all_traces_identical: bool, defensibility_note: string, duplicated_source_sites_per_sign: str (... 446 chars omitted)
child 0, all_traces_identical: bool
child 1, defensibility_note: string
child 2, duplicated_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 3, morphology_segments: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 4, n_traces: int64
child 5, policy: string
child 6, source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 7, status: string
child 8, unique_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 9, unused_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 10, used_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
intervention: null
intervention_dose: null
kind: string
morphology_id: string
morphology_path: string
samples: int64
shard_index: int64
teacher_balance_label: string
version: int64
shards: list<item: struct<count: int64, file: string, sample_ids: list<item: string>>>
child 0, item: struct<count: int64, file: string, sample_ids: list<item: string>>
child 0, count: int64
child 1, file: string
child 2, sample_ids: list<item: string>
child 0, item: string
to
{'shards': List({'count': Value('int64'), 'file': Value('string'), 'sample_ids': List(Value('string'))}), 'version': Value('int64')}
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 483, 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 2951, in __iter__
for key, example in ex_iterable:
^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2461, in __iter__
for key, pa_table in self._iter_arrow():
~~~~~~~~~~~~~~~~^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 2486, 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 547, in _iter_arrow
for key, pa_table in iterator:
^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/iterable_dataset.py", line 430, 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 2378, in table_cast
return cast_table_to_schema(table, schema)
File "/usr/local/lib/python3.14/site-packages/datasets/table.py", line 2306, in cast_table_to_schema
raise CastError(
...<3 lines>...
)
datasets.table.CastError: Couldn't cast
backend: string
coreneuron_gpu: bool
duration_ms: int64
elapsed_seconds: double
exc_gmax_scale: double
generator: struct<backend: string, biophysics_hoc_sha256: string, code_revision: struct<commit: string, dirty: (... 456 chars omitted)
child 0, backend: string
child 1, biophysics_hoc_sha256: string
child 2, code_revision: struct<commit: string, dirty: bool>
child 0, commit: string
child 1, dirty: bool
child 3, data_version: string
child 4, dt_ms: double
child 5, exc_gmax_scale: double
child 6, inh_gmax_scale: double
child 7, input_routing: string
child 8, input_sampler: string
child 9, integrator: string
child 10, mechanism_files: list<item: string>
child 0, item: string
child 11, mechanisms_sha256: string
child 12, morphology_sha256: string
child 13, neuron_version: string
child 14, nseg_policy: string
child 15, soma_samples_per_ms: int64
child 16, spike_label_rule: string
child 17, synapse_delay_ms: double
child 18, synapses: string
child 19, teacher: string
child 20, template_hoc_sha256: string
child 21, v_init_mv: double
inh_gmax_scale: double
input_event_policy: string
input_routing: struct<all_traces_identical: bool, defensibility_note: string, duplicated_source_sites_per_sign: str (... 446 chars omitted)
child 0, all_traces_identical: bool
child 1, defensibility_note: string
child 2, duplicated_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 3, morphology_segments: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 4, n_traces: int64
child 5, policy: string
child 6, source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 7, status: string
child 8, unique_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 9, unused_source_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
child 10, used_sites_per_sign: struct<max: int64, mean: double, min: int64>
child 0, max: int64
child 1, mean: double
child 2, min: int64
intervention: null
intervention_dose: null
kind: string
morphology_id: string
morphology_path: string
samples: int64
shard_index: int64
teacher_balance_label: string
version: int64
shards: list<item: struct<count: int64, file: string, sample_ids: list<item: string>>>
child 0, item: struct<count: int64, file: string, sample_ids: list<item: string>>
child 0, count: int64
child 1, file: string
child 2, sample_ids: list<item: string>
child 0, item: string
to
{'shards': List({'count': Value('int64'), 'file': Value('string'), 'sample_ids': List(Value('string'))}), 'version': Value('int64')}
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.
AxoBench v2
AxoBench is a benchmark for data-driven surrogates of layer-5 pyramidal neurons: given six seconds of synaptic input events, predict the somatic voltage and spikes of a detailed NEURON model of the cell. Version 2 covers 15 cells, adds paired interventions at three doses each, and stores the somatic voltage at 4 kHz in addition to the 1 ms targets.
Variants
Each variant is a self-contained dataset root in its own top-level folder.
| Folder | Status | Traces per training cell | Size |
|---|---|---|---|
minimal/ |
released (tag minimal-v2.0) |
2,000 train, 250 val, 250 test | 14.6 GB |
full/ |
released (tag full-v2.0) |
8,000 train, 250 val, 250 test | 35.6 GB |
full/ contains every minimal/ shard unchanged, plus 6,000 more training
traces per training cell. Its val/, test/ and interventions/ are the
same files as in minimal/, so scores on the two variants are directly
comparable. The extra shards were generated with the same simulator, gains and
input statistics, and take shard indices from 20,000 up, so no index or seed
of minimal/ is reused.
Download with the axobench package (axobench download-data --variant full,
or axobench.hub.download_dataset), or fetch single folders with
huggingface_hub.snapshot_download(..., allow_patterns=["full/val/*"]).
Cells
- 14 Allen Cell Types all-active models of mouse layer-5 cells with intact apical dendrites (Gouwens et al. 2018), each with its fitted biophysics and a per-cell excitatory gain calibrated to a common firing rate.
- The NeuronIO layer-5b cell (Hay et al. 2011,
neuronio_hay_cell1) as the anchor to earlier work.
Three Allen cells (354190013, 480353286, 488683425) are held out: they appear
only in test (zero-shot track). morphologies.json lists every cell with
its source and held-out flag; morphologies/ holds the Allen SWC files.
Layout of minimal/ and full/
| Folder | Content |
|---|---|
train/<cell>/ |
minimal/: 6,000 shards, 24,000 traces (12 training cells x 2,000); full/: 24,000 shards, 96,000 traces (12 x 8,000) |
val/<cell>/ |
756 shards, 3,000 traces (12 x 250) |
test/<cell>/ |
945 shards, 3,750 traces (15 x 250) |
interventions/<condition>_<dose>/ |
15 folders, 600 pairs each (40 per cell), 9,000 pairs in total |
morphologies/, morphologies.json |
cell index and reconstructions |
dataset_package_manifest.json |
counts per split, cell and condition; generator settings and gains |
checksums.sha256 |
SHA-256 of every file in the variant |
Interventions: event dropout, excitatory dropout and inhibitory dropout at 10, 35 and 70%; site silencing at 10, 25 and 50%; temporal jitter of 1, 2 and 8 ms.
Shard schema
Each .npz shard has a JSON sidecar with the generator settings. Each split
and intervention folder has a manifest.json that lists its shards (paths
relative to the folder; split shards sit in one subfolder per cell) and sample
ids.
inputs:(n, 6000, 1278)int8, input events per 1 ms bin on 639 excitatory and 639 inhibitory synapse sites.targets:(n, 6000, 2)float32 at 1 ms: spike indicator (0/1) and the NeuronIO-style somatic target, (min(V, -55 mV) + 67.7 mV) / 10.soma_mv:(n, 6000)raw somatic voltage (mV) at 1 ms.soma_mv_hr:(n, 24000)raw somatic voltage (mV) at 4 kHz.- Intervention shards hold the same arrays with
baseline_andintervention_prefixes, pluschanged_event_mask.
Withheld data
A confirmation split (private-test, 125 traces per cell) is not published.
Predictions on it are scored on request, rate-limited.
License and attribution
The data are released under CC BY-NC 4.0. The Allen cells are simulated on reconstructions and models from the Allen Cell Types Database, whose Terms of Use allow derived works for research and other noncommercial purposes only. Commercial use needs written permission from the Allen Institute.
If you use these data, please cite:
- Allen Institute for Brain Science (2015). Allen Cell Types Database [dataset]. Available from celltypes.brain-map.org.
- Gouwens, N. W., et al. (2018). Systematic generation of biophysically detailed models for diverse cortical neuron types. Nature Communications, 9, 710. https://doi.org/10.1038/s41467-017-02718-3
- Hay, E., Hill, S., Schürmann, F., Markram, H., & Segev, I. (2011). Models of neocortical layer 5b pyramidal cells capturing a wide range of dendritic and perisomatic active properties. PLoS Computational Biology, 7(7), e1002107. https://doi.org/10.1371/journal.pcbi.1002107
- Beniaguev, D., Segev, I., & London, M. (2021). Single cortical neurons as deep artificial neural networks. Neuron, 109(17), 2727–2739.e3. https://doi.org/10.1016/j.neuron.2021.07.002 (input statistics and generator design)
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