The dataset viewer is not available for this split.
Error code: StreamingRowsError
Exception: TypeError
Message: Couldn't cast array of type
struct<hellaswag: struct<name: string, alias: string, sample_len: int64, acc,none: double, acc_stderr,none: string, acc_norm,none: double, acc_norm_stderr,none: string>>
to
{'arc_challenge': {'name': Value('string'), 'alias': Value('string'), 'sample_len': Value('int64'), 'acc,none': Value('float64'), 'acc_stderr,none': Value('string'), 'acc_norm,none': Value('float64'), 'acc_norm_stderr,none': Value('string')}}
Traceback: Traceback (most recent call last):
File "/src/services/worker/src/worker/utils.py", line 149, 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 129, 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 489, 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 2303, in cast_table_to_schema
cast_array_to_feature(
~~~~~~~~~~~~~~~~~~~~~^
table[name] if name in table_column_names else pa.array([None] * len(table), type=schema.field(name).type),
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
feature,
^^^^^^^^
)
^
File "/usr/local/lib/python3.14/site-packages/datasets/table.py", line 1852, in wrapper
return pa.chunked_array([func(chunk, *args, **kwargs) for chunk in array.chunks])
~~~~^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.14/site-packages/datasets/table.py", line 2149, in cast_array_to_feature
raise TypeError(f"Couldn't cast array of type\n{_short_str(array.type)}\nto\n{_short_str(feature)}")
TypeError: Couldn't cast array of type
struct<hellaswag: struct<name: string, alias: string, sample_len: int64, acc,none: double, acc_stderr,none: string, acc_norm,none: double, acc_norm_stderr,none: string>>
to
{'arc_challenge': {'name': Value('string'), 'alias': Value('string'), 'sample_len': Value('int64'), 'acc,none': Value('float64'), 'acc_stderr,none': Value('string'), 'acc_norm,none': Value('float64'), 'acc_norm_stderr,none': Value('string')}}Need help to make the dataset viewer work? Make sure to review how to configure the dataset viewer, and open a discussion for direct support.
gemma4-bio
Code and per-example results for the paper:
Scientific Data Composition as a Capability-Shaping Mechanism for Foundation Models: Evidence from Biological Continued Pretraining — Liang Wang (HUST).
The study has two parts on a 26B-parameter Mixture-of-Experts model (Gemma-4-26B-A4B):
- Part I — training-free re-analysis of one checkpoint lineage (instruction-tuned base → biological CPT → SFT) across four capability axes.
- Part II — a controlled seven-model experiment: continue pretraining the same base under one fixed recipe, varying only the data mixture (0/5/20/50% biological share, plus a protein/DNA composition ablation), turning the observational claim into a causal one.
- Part III — a small-model, matched-compute causal probe (GPT-2, 3 seeds): asks the reverse question — does biological CPT feed anything back into natural-language understanding — in a regime with capability headroom the 26B model lacks.
- Part IV — robustness and mechanism: does the Part II pattern hold across a 10× model-scale range (2.3B–26B)? does explicit replay recover anything uniform mixing might have cost? does mixture ratio operate through the same router-reorganization mechanism as full CPT?
Key finding (Part I)
Biological CPT does not cause catastrophic forgetting; it lifts the model on axes unrelated to biology, and SFT then narrows it back — a consistent CPT-lifts / SFT-narrows division of labor.
| axis | metric | Base (it) | BioCPT | BioCPT+SFT |
|---|---|---|---|---|
| General | MMLU (5-shot) | 0.646 | 0.776 | 0.635 |
| General | ARC-C acc (25-shot) | 0.367 | 0.700 | 0.382 |
| General | HellaSwag norm (10-shot) | 0.488 | 0.855 | 0.486 |
| General | TruthfulQA-mc2 | 0.533 | 0.445 | 0.562 |
| Coding | MBPP pass@1 (3-shot) | 0.332 | 0.630 | 0.348 |
| Biology | BixBench-TF (MCC) | 0.232 | 0.924 | 0.361 |
| Reasoning | CoT chain length (tok) | 108.8 | 64.4 | 125.8 |
| Reasoning | backtracks / gen | 0.370 | 0.006 | 0.396 |
Vocabulary expansion alone (it → it-bio) is free (< 0.4 pt on every general metric), so the gains are attributable to CPT, not the tokenizer.
Key finding (Part II — controlled mixture experiment)
Varying only the CPT data mixture (100M tokens each, one fixed recipe, from it-bio):
| model | bio% | MMLU | GSM8K | homology-std (MCC) | homology-remote (MCC) | BixBench (MCC) |
|---|---|---|---|---|---|---|
| M0-base | 0 | 0.802 | 0.873 | 0.228 | −0.023 | 0.850 |
| M1-bio5 | 5 | 0.801 | 0.867 | 0.270 | −0.055 | 0.882 |
| M2-bio20 | 20 | 0.800 | 0.867 | 0.217 | −0.074 | 1.000 |
| M3-bio50 | 50 | 0.796 | 0.861 | 0.375 | 0.088 | 1.000 |
Raising biological share to 50% preserves the general axis (MMLU −0.6 pt, GSM8K −1.2 pt) while the biology axis rises monotonically — the two do not trade off. A composition ablation at fixed 20% share shows DNA most improves remote homology while protein most improves BixBench: the type of scientific data selects which capability is amplified. Data mixture is a controllable, general-preserving lever on the capability profile.
Key finding (Part III — small-model matched-compute causal probe)
GPT-2 (124M): shared warmup (nl_base, 300M NL tokens), then two arms continued for an
identical 200M tokens / 3,051 steps / optimizer schedule — only content differs (NL-only vs.
50/50 protein+DNA). Mean over 3 seeds:
| family | task | NL-arm | Bio-arm | Δ (Bio−NL), mean±sd |
|---|---|---|---|---|
| Structural | PAWS-en (paraphrase detection) | 0.498 | 0.529 | +0.031 ± 0.009 |
| Structural | Anagrams / cycle-letters / insertion / reversed (character-level) | 0.000 | 0.000 | floor at this scale (uninformative) |
| Knowledge | HellaSwag | 0.291 | 0.285 | −0.006 ± 0.000 |
| Knowledge | LAMBADA (long-range discourse) | 0.333 | 0.188 | −0.146 ± 0.004 |
A real, reproducible transfer (all 3 seeds agree in sign) to the direct NL counterpart of protein-homology detection — but a genuine cost to long-range discourse, and the character-level battery is simply unmeasurable at 124M (both arms floor at 0, consistent with the original GPT-3 paper's own report of this floor below tens-of-billions of parameters). Reported as a partial, not uniform, dissociation.
Key finding (Part IV — robustness and mechanism)
Scale robustness. Repeating the Part II text-only-vs-bio50 contrast at two smaller dense Gemma-4 sizes (E2B 2.3B, E4B 4.5B) alongside the 26B MoE result:
| model | MMLU (text→bio50) | BixBench MCC (text→bio50) |
|---|---|---|
| E2B (2.3B) | 0.576 → 0.578 (+0.2 pt) | 0.479 → 0.623 (+14.4 pt) |
| E4B (4.5B) | 0.694 → 0.695 (+0.1 pt) | 0.680 → 0.781 (+10.1 pt) |
| 26B-A4B | 0.802 → 0.796 (−0.6 pt) | 0.850 → 1.000 (+15.0 pt) |
General-preservation and the BixBench lift both hold across a 10× parameter range. Homology (harder, lower-sample-count) is noisier below 26B — likely a capability-floor effect on weaker dense models, reported honestly rather than smoothed over.
Replay control. At fixed 50% biological share, 100M tokens (26B), explicit end-of-training text replay (10%/20% of tokens) vs. the uniformly-shuffled baseline:
| model | replay | MMLU | homology-std MCC | BixBench MCC |
|---|---|---|---|---|
| M3-bio50 | 0% (uniform) | 0.796 | 0.375 | 1.000 |
| R1 | 10% (tail) | 0.800 | 0.318 | 1.000 |
| R2 | 20% (tail) | 0.795 | 0.266 | 0.873 |
The general axis is already flat without replay — there was nothing to recover. Replay does not help and mildly hurts the biology axis (fewer effective bio tokens as replay fraction rises). A clean negative result.
Router mechanism. Forward-hook analysis of all 30 MoE routers across every checkpoint: the full-CPT lineage (it-bio→BioCPT, 8.7B tokens) shows a large increase in biology-vs-language routing divergence (0.219→0.451), but the Phase-2 LoRA mixture sweep (M0→M3, 100M tokens) shows no routing dose-response (0.376–0.385, flat) despite a clear capability dose-response — capability shaping and routing reorganization are dissociable mechanisms that converge only at large (full-parameter) training budgets.
Checkpoints & data
- BioCPT (merged):
dnagpt/OmniGene-4-CPT-v2-merged - Data / per-example outputs:
dnagpt/OmniGene-4-bio - Base is the public Gemma-4-26B-A4B instruction-tuned model.
Repository layout
scripts/ evaluation harness (all reproduce on a single 96GB GPU, sm_120 grouped-mm guard)
run_general.py MMLU / ARC / HellaSwag / TruthfulQA (loglikelihood MC)
run_coding.py HumanEval / MBPP (generative + execution)
run_bio_loglik.py BixBench / homology (format-robust loglikelihood)
run_cot.py GSM8K chain-of-thought behavior diagnostics
make_figs.py paper figures
run_phase1_*.sh full sweeps over the 4 checkpoints
results/ per-(checkpoint, task) JSON + summary tables (PHASE1_*.md)
scripts_phase2/ controlled mixture-CPT experiment (Part II)
prepare_pools.py tokenize each source into a reusable pool
run_cpt_mix.py QLoRA CPT at a given data mixture (TAG, MIX, MIX_TOKENS)
launch_parallel.sh train the 7 models, one per GPU (auto-detects card count)
bt2_load.py reconstruct a CPT model (base + LoRA + trained embedding)
run_eval.py / run_eval_bio.py general + biology eval by model tag
collect_results.py / make_figs.py summary table + figures
sm120_guard.py dtype-safe MoE fallback for Blackwell (sm_120) training
results_phase2/ per-(model, task) JSON + phase2_summary.csv + figures
scripts_phase3/ small-model matched-compute causal probe (Part III)
prepare_pools.py tokenize NL/protein/DNA sources into GPT-2 pools
train.py warmup or matched-compute continuation (STAGE, MIX, TOKENS)
run_tier1.sh warmup -> 3 seeds x {NL,bio} arms, one GPU each
run_eval.py / launch_eval.sh NL-probe battery by model tag
collect_results.py per-seed delta + mean/sd, dissociation verdict
*_local.yaml custom lm-eval tasks for the GPT-3-paper character battery
(mirrors EleutherAI/unscramble, whose HF loading script is
no longer supported by current `datasets`)
results_phase3/ per-(model, task) JSON + tier1_summary.json
scripts_phase4/ robustness + mechanism follow-ups (Part IV)
prepare_pools_gemma_small.py tokenize sources w/ E2B/E4B native tokenizer
run_scaling.py / run_scaling.sh LoRA CPT on E2B/E4B (dense, no router)
scaling_load.py reconstruct an E2B/E4B CPT model for eval
run_eval_scaling.py / run_eval_bio_scaling.py / launch_eval_scaling.sh
run_replay.sh replay-control sweep (reuses run_cpt_mix.py
with REPLAY_TAIL_FRAC/REPLAY_TEXT_SOURCE)
run_eval_replay.sh eval the replay-control models
run_router_analysis.py / run_router_sweep.sh 30-router forward-hook JS
divergence analysis across every checkpoint
make_figs_part4.py scaling / replay / router figures
results_phase4/ scaling + replay eval JSON, router/ = per-checkpoint routing reports
paper/ LaTeX source (Part I--IV sections), figures, compiled PDF
Reproducing
All benchmarks are public (MMLU, ARC, HellaSwag, TruthfulQA, MBPP, HumanEval, GSM8K, BixBench);
no proprietary data. General/coding use lm-evaluation-harness 0.4.12 at community-standard
few-shot. Example:
python scripts/run_general.py --ckpt <checkpoint> --tag mymodel \
--tasks mmlu arc_challenge hellaswag truthfulqa_mc2 --out-dir results
Note: on Blackwell (sm_120) the scripts install a grouped-mm guard
(transformers.integrations.moe._can_use_grouped_mm = lambda *a, **k: False) before any forward.
Citation
@article{wang2026biocpt,
title = {Scientific Data Composition as a Capability-Shaping Mechanism for
Foundation Models: Evidence from Biological Continued Pretraining},
author = {Wang, Liang},
year = {2026},
note = {preprint}
}
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