Georgakopoulos-Soares-lab/superweights

Python

1

48 commits

updated Sep 12, 2026

See the code

README

Structure is not mechanism

High-gain gated-FFN rows across text and genomic foundation models

Code, artifacts and preregistrations for the paper of this title. The manuscript itself is not in this repository; it ships with the publication.

The question. A handful of "super weights" in text LLMs can be catastrophically important. Do analogous structures recur in genomic foundation models — and, more sharply, does a high-gain row's structural prominence tell you anything about its causal importance?

The answer, across a preregistered 22-model causal census and focused mechanistic case studies, is that three quantities routinely conflated in this literature are distinct:

STRUCTURAL GEOMETRY  ≠  FUNCTIONAL CRITICALITY  ≠  CAUSAL RESPONSE COMPLEXITY

Start here

Every claim → its code → its artifactsdocs/EXPERIMENT_MAP.md — 21 experiments, machine-checked
Reproduce anythingpipelines/ — idempotent, GPU-parallel runners
Panel-by-panel figure provenanceexperiments/figures/FIGURE_PROVENANCE.md
Supplementary tables S1–S8results/supplementary/
Preregistrations (12, content-locked)docs/prereg/ — python src/prereg_lock.py verify --all

What the paper establishes

findingkey numbers
High-gain gated-FFN rows are a recurrent structural phenotype across text and genomic models23-model structural panel; near-rank-1 candidates in both encoders and decoders
Activation-selected candidates are functionally enriched over same-layer controlscandidate beats the within-model control median in 18/22 models at ε=0.5 and 20/22 at ε=1.0
That enrichment survives a stricter, purely weight-space controlvs the 5 highest-Frobenius same-layer rows: candidate retains its advantage in 20/22 (ε=0.5) and 19/22 (ε=1.0); those high-norm rows are themselves near-inert (+0.035%, +0.110%)
Structural geometry does not predict effect size — the central negative resultfull-ablation effects span −0.79% to +698.87%; q1 vs signed effect ρ = 0.074 (95% CI −0.391 to 0.513); operator magnitude likewise fails
The activation ratio is two-regime, replicated in a genomic and a text decoderbelow the ≥5 accept threshold ρ = +0.040 (p=0.86) genomic, −0.584 (p=0.005) text; above it ρ = +0.639 and +0.975. n=36 rows/model
Ratio rank ≠ causal importanceSmolLM2-1.7B L7: the row ranked 4th by ratio is 130× more damaging than the row ranked 2nd. OLMo-7B: the ratio-argmax coordinate is 47× less damaging than the published one
Causal organization differs by model, and interaction sign is not fixedDNABERT-2: two near-inert rows, joint epistasis +2.0118, held-out R² 0.888 (F3) vs 0.517 (F2). SmolLM2 L7: super-additive, sub-additive, and near-total masking all within one layer
GENERator's effect is position-localized at BOS, and not direction-specificrestoring the BOS contribution rescues essentially all damage; a damage-matched random direction reproduces the GC phenotype
Detector provenance is closed for all 22 census rows16 by the current rule; Llama-7B and Mistral-7B verified at global rank 1/131,072; OLMo-7B, DNABERT-2 and NTv3 characterised disagreements

Installation

git clone https://github.com/Georgakopoulos-Soares-lab/superweights.git
cd superweights
pip install -r requirements.txt
export PYTHONPATH=.          # required: scripts import the shared library as `src.*`

All commands below assume PYTHONPATH=. and the repository root as the working directory.

Three environments are needed, because the model families pin incompatible transformers:

environmenttransformersused for
main≥ 4.40 (tested 5.5.0)GENERator, NTv3, all text decoders, the census, every analysis
dnabert4.29.2DNABERT-2 — its remote code predates the Transformers-5 config API
evo4.48.1Evo1

Running DNABERT-2 under the main environment fails with BertConfig has no attribute pad_token_id. That is the wrong-environment signature, not a bug.

Data

inputstatus
WikiText-2 (text endpoints)Committed at frozen_inputs/, sha256 5f1bea06…. The same file the census resolved through datasets, so text endpoints run offline.
hg38 (genomic endpoints)Not committed. Place or symlink at data/reference/hg38/hg38.fa.
GUE (downstream tasks)Not committed. Point $GUE_ROOT at the extracted tree.
CheckpointsPinned Hugging Face revisions, one per model, in audit/census_master.csv.

Other large public inputs are documented rather than vendored — see data/README.md.

Reproducing the paper

One row per object in the paper. Every artifact path below was verified to exist in this repository; where an input is gitignored and therefore absent from a clone, the row says so and names the command that regenerates it.

A note on filenames. Moving the within-layer section ahead of the DNABERT-2 section shifted the figure numbers after it by one, but the script filenames were not renamed — renaming them risks breaking the literal-path sys.path inserts this repository depends on (see tests/test_entrypoints.py). So fig3_dnabert.py renders Figure 4 and fig4_generator.py renders Figure 5. The offset is intentional and is flagged on each affected row.

Main figures

paper objectcommandartifactnotes
Figure 1 — structural panelpython experiments/figures/fig1_structural.pyexperiments/figures/main/fig1_structural.{pdf,png}Panel A is the retrospective diagonal-proxy calibration; B and C the exact operator metrics
Figure 2 — 22-model causal censuspython experiments/figures/fig2_causal.pyexperiments/figures/main/fig2_causal.{pdf,png}Panels A/B effects, C the q₁ dissociation, D the top-norm control
Figure 3 — within-layer sweepbash pipelines/fig5_within_layer.shresults/analyses/within_layer_sweep/fig_within_model_slope_2panel.{pdf,png}⚠ pipeline filename retains the earlier figure number
Figure 4 — DNABERT-2 multi-row causal responsepython experiments/figures/fig3_dnabert.pyexperiments/figures/main/fig3_dnabert.{pdf,png}⚠ script filename says fig3
Figure 5 — GENERator BOS mediationpython experiments/figures/fig4_generator.pyexperiments/figures/main/fig4_generator.{pdf,png}⚠ script filename says fig4; companion panel from fig4_generator_specificity.py

Supplementary figures

paper objectcommandartifact
Fig S1 — structural/control detailpython experiments/figures/supplement/fig_s1_structural_detail.pyexperiments/figures/supplement/fig_s1_structural_detail.{pdf,png}
Fig S2 — damage-matched random directionpython experiments/figures/supplement/fig_s2_random_direction.pyexperiments/figures/supplement/fig_s2_random_direction.{pdf,png}

Supplementary tables

S2, S3 and S6–S8 are generated; S1, S4 and S5 are reformatted verbatim from the audit and are not rebuilt. One command produces all five generated tables.

python scripts/census_analysis/build_supplementary_tables.py
tableartifactrows
S1 — model panel and provenanceresults/supplementary/S1_model_panel_provenance.{tsv,md,csv}22
S2 — structural metrics + 24-input stabilityresults/supplementary/S2_structural_metrics_stability.{tsv,md}22
S3 — causal census + disagreement coordinatesresults/supplementary/S3_causal_census_disagreements.{tsv,md}49
S4 — structure–function correlationsresults/supplementary/S4_structure_function_correlations.{tsv,md,csv}16
S5 — GENERator conditionsresults/supplementary/S5_generator_conditions.{tsv,md,csv}106
S6 — DNABERT-2 tomographyresults/supplementary/S6_dnabert2_tomography.{tsv,md}98
S7 — within-layer sweepresults/supplementary/S7_within_layer_sweep.{tsv,md}72
S8 — two critical rows + geometryresults/supplementary/S8_two_critical_rows.{tsv,md}13

Results in the text, not in a figure

claimcommandartifact
Two critical rows in one layer, and the masking interactionpython scripts/within_layer_sweep/run_smollm2_second_row_epistasis.pyresults/analyses/within_layer_sweep/smollm2_second_row_epistasis.json
Row geometry against a same-layer null (data-free, no GPU)python scripts/within_layer_sweep/run_smollm2_row_geometry.pyresults/analyses/within_layer_sweep/smollm2_161_749_geometry.json
Selection-rule resolution for every legacy candidatebash pipelines/detector_provenance.shresults/analyses/detector_provenance/EXP2_LEGACY_DETECTOR_RESOLUTION.md
Cohort structure–function correlationspython scripts/census_analysis/run_activation_vs_causality.pyresults/analyses/census_analysis/activation_vs_causality.tsv

The authoritative, machine-checked mapping is docs/EXPERIMENT_MAP.md (21 experiments) and, panel by panel, experiments/figures/FIGURE_PROVENANCE.md. This table surfaces them; it does not replace them. python scripts/build_experiment_map.py re-verifies that every script and artifact named there still exists.

Running the pipelines

Prefer the pipelines. Each skips stages whose output already exists, so an interrupted run resumes and a finished one costs nothing; FORCE=1 recomputes.

bash pipelines/census.sh                 # the preregistered 22-model causal census (restartable)
bash pipelines/census.sh dnabert2 ntv3   # ...or a subset
bash pipelines/detector_provenance.sh    # selection-rule resolution; runs its positive control first
bash pipelines/fig5_within_layer.sh      # the within-layer sweeps and second critical row
                                         # (filename retains an earlier figure number)

Individual stages:

# structural panel and causal census
python experiments/E11_scale_ladder/run_model.py --model <slug>
python experiments/E13_full_cohort_causal_census/run_singleton_census.py --model <slug>

# mechanism case studies
python experiments/E9_mechanistic_tomography/run_fit_observers.py
python experiments/E12_generator_degradation_control/run_bos_mediation_main.py

# within-layer sweeps
python scripts/within_layer_sweep/run_within_model_slope_text.py     # SmolLM2-1.7B, ~7 min, 1 GPU
python scripts/within_layer_sweep/run_smollm2_row_geometry.py        # data-free, no GPU

# supplementary tables S2, S3, S6-S8 (rebuilt from committed artifacts)
python scripts/census_analysis/build_supplementary_tables.py

# two flags that are REQUIRED and silently wrong if omitted
python scripts/detection/run_detection.py --model ntv3 --pad_to_multiple 256   # stride-256 U-Net
python scripts/evaluation/run_gue_multiseed.py --model ntv3 --max_length 400   # nucleotide tokenizer

Verify the repository's own invariants:

python scripts/build_experiment_map.py    # every claim's code and artifacts exist
python src/prereg_lock.py verify --all    # 12 preregistrations, content-locked
pytest tests/                             # unit tests + every CLI entry point starts

Repository map

experiments/ contains the preregistered harnesses (E1–E13, each with the preregistration it was run under in docs/prereg/); scripts/ contains analyses developed after preregistration. The split is deliberate: it lets a reader see at a glance which analyses were locked in advance and which came later.

pathcontents
experiments/E1–E13The preregistered harnesses, one directory per experiment line. Not edited after the fact to make later results come out differently. E5_dimensionality/ is a cut line whose library is still imported by three audit builders — see its README.
experiments/figures/Figure render scripts, output, source_data/ (the exact plotted values), and FIGURE_PROVENANCE.md
scripts/detection/Super-row detection and selection-rule resolution
scripts/mechanism/BOS mediation, attention sink, special-token dependence, matched replacements
scripts/within_layer_sweep/The graded within-layer sweeps, the second critical row, Figure 5
scripts/census_analysis/Cohort structure–function correlations; the supplementary-table builder
scripts/negative_results/Experiments whose only result is a null — see its README
scripts/evaluation/GUE downstream evaluation
pipelines/Reproduction runners
src/Shared library: activation capture, ablation, spike detection, DNA probes, the prereg lock
models/, configs/Per-model wrappers and YAML, loaded dynamically via WRAPPER_MAP
stubs/Import shims, not PEP 484 type stubs — they let wrappers for models outside the paper's panel import without heavy optional dependencies. See stubs/README.md.
audit/The verification record: census_master.csv (22 models × 44 columns) is the canonical table. Three adversarial passes; see its README.
results/Artifacts in four groups — experiments/ (per harness), analyses/ (derived), negative_results/, supplementary/ (S1–S8). Gitignored by default; files backing a reported number are force-added. See its README.
docs/The experiment map and the 12 locked preregistrations
frozen_inputs/, data/, tests/Content-hashed inputs, small reference files, tests

Provenance and known limitations

Stated plainly, because a reader will find them anyway.

  1. Some raw artifacts are not committed. Several were produced on a cluster and never transferred. For every affected item the committed figure source-data snapshot under experiments/figures/source_data/ carries the plotted values, so each reported number remains inspectable.
  2. NTv3's original weight revision was not recorded and is not recoverable. Resolved Hub commits exist for 21 of 22 models.
  3. One n=10 subgroup is fragile. The text-decoder correlation moves from ρ=0.770 to 0.673 under an OLMo coordinate substitution, with a 95% lower bound of +0.032. It should not be read as independently robust; the 22-model result is insensitive to the substitution.
  4. Experiment lines that the paper does not report are not in the working tree. Their preregistrations are retained in docs/prereg/, each with an explicit disposition, rather than deleted — see docs/prereg/README.md. E5_dimensionality/ keeps one file, a library three audit builders import.
  5. The preregistrations record what was planned, including paths that predate later directory renames. They are content-locked and were deliberately never rewritten to match.

Citation

See CITATION.cff. Released under the MIT License (LICENSE).

Prior work this builds on: Yu M, Wang D, Shan Q, Reed CJ, Wan A. The Super Weight in Large Language Models. arXiv:2411.07191 (2024).

Georgakopoulos-Soares-lab/superweights

Python

1

48 commits

updated Sep 12, 2026

See the code

README

Structure is not mechanism

High-gain gated-FFN rows across text and genomic foundation models

Code, artifacts and preregistrations for the paper of this title. The manuscript itself is not in this repository; it ships with the publication.

The question. A handful of "super weights" in text LLMs can be catastrophically important. Do analogous structures recur in genomic foundation models — and, more sharply, does a high-gain row's structural prominence tell you anything about its causal importance?

The answer, across a preregistered 22-model causal census and focused mechanistic case studies, is that three quantities routinely conflated in this literature are distinct:

STRUCTURAL GEOMETRY  ≠  FUNCTIONAL CRITICALITY  ≠  CAUSAL RESPONSE COMPLEXITY

Start here

Every claim → its code → its artifactsdocs/EXPERIMENT_MAP.md — 21 experiments, machine-checked
Reproduce anythingpipelines/ — idempotent, GPU-parallel runners
Panel-by-panel figure provenanceexperiments/figures/FIGURE_PROVENANCE.md
Supplementary tables S1–S8results/supplementary/
Preregistrations (12, content-locked)docs/prereg/ — python src/prereg_lock.py verify --all

What the paper establishes

findingkey numbers
High-gain gated-FFN rows are a recurrent structural phenotype across text and genomic models23-model structural panel; near-rank-1 candidates in both encoders and decoders
Activation-selected candidates are functionally enriched over same-layer controlscandidate beats the within-model control median in 18/22 models at ε=0.5 and 20/22 at ε=1.0
That enrichment survives a stricter, purely weight-space controlvs the 5 highest-Frobenius same-layer rows: candidate retains its advantage in 20/22 (ε=0.5) and 19/22 (ε=1.0); those high-norm rows are themselves near-inert (+0.035%, +0.110%)
Structural geometry does not predict effect size — the central negative resultfull-ablation effects span −0.79% to +698.87%; q1 vs signed effect ρ = 0.074 (95% CI −0.391 to 0.513); operator magnitude likewise fails
The activation ratio is two-regime, replicated in a genomic and a text decoderbelow the ≥5 accept threshold ρ = +0.040 (p=0.86) genomic, −0.584 (p=0.005) text; above it ρ = +0.639 and +0.975. n=36 rows/model
Ratio rank ≠ causal importanceSmolLM2-1.7B L7: the row ranked 4th by ratio is 130× more damaging than the row ranked 2nd. OLMo-7B: the ratio-argmax coordinate is 47× less damaging than the published one
Causal organization differs by model, and interaction sign is not fixedDNABERT-2: two near-inert rows, joint epistasis +2.0118, held-out R² 0.888 (F3) vs 0.517 (F2). SmolLM2 L7: super-additive, sub-additive, and near-total masking all within one layer
GENERator's effect is position-localized at BOS, and not direction-specificrestoring the BOS contribution rescues essentially all damage; a damage-matched random direction reproduces the GC phenotype
Detector provenance is closed for all 22 census rows16 by the current rule; Llama-7B and Mistral-7B verified at global rank 1/131,072; OLMo-7B, DNABERT-2 and NTv3 characterised disagreements

Installation

git clone https://github.com/Georgakopoulos-Soares-lab/superweights.git
cd superweights
pip install -r requirements.txt
export PYTHONPATH=.          # required: scripts import the shared library as `src.*`

All commands below assume PYTHONPATH=. and the repository root as the working directory.

Three environments are needed, because the model families pin incompatible transformers:

environmenttransformersused for
main≥ 4.40 (tested 5.5.0)GENERator, NTv3, all text decoders, the census, every analysis
dnabert4.29.2DNABERT-2 — its remote code predates the Transformers-5 config API
evo4.48.1Evo1

Running DNABERT-2 under the main environment fails with BertConfig has no attribute pad_token_id. That is the wrong-environment signature, not a bug.

Data

inputstatus
WikiText-2 (text endpoints)Committed at frozen_inputs/, sha256 5f1bea06…. The same file the census resolved through datasets, so text endpoints run offline.
hg38 (genomic endpoints)Not committed. Place or symlink at data/reference/hg38/hg38.fa.
GUE (downstream tasks)Not committed. Point $GUE_ROOT at the extracted tree.
CheckpointsPinned Hugging Face revisions, one per model, in audit/census_master.csv.

Other large public inputs are documented rather than vendored — see data/README.md.

Reproducing the paper

One row per object in the paper. Every artifact path below was verified to exist in this repository; where an input is gitignored and therefore absent from a clone, the row says so and names the command that regenerates it.

A note on filenames. Moving the within-layer section ahead of the DNABERT-2 section shifted the figure numbers after it by one, but the script filenames were not renamed — renaming them risks breaking the literal-path sys.path inserts this repository depends on (see tests/test_entrypoints.py). So fig3_dnabert.py renders Figure 4 and fig4_generator.py renders Figure 5. The offset is intentional and is flagged on each affected row.

Main figures

paper objectcommandartifactnotes
Figure 1 — structural panelpython experiments/figures/fig1_structural.pyexperiments/figures/main/fig1_structural.{pdf,png}Panel A is the retrospective diagonal-proxy calibration; B and C the exact operator metrics
Figure 2 — 22-model causal censuspython experiments/figures/fig2_causal.pyexperiments/figures/main/fig2_causal.{pdf,png}Panels A/B effects, C the q₁ dissociation, D the top-norm control
Figure 3 — within-layer sweepbash pipelines/fig5_within_layer.shresults/analyses/within_layer_sweep/fig_within_model_slope_2panel.{pdf,png}⚠ pipeline filename retains the earlier figure number
Figure 4 — DNABERT-2 multi-row causal responsepython experiments/figures/fig3_dnabert.pyexperiments/figures/main/fig3_dnabert.{pdf,png}⚠ script filename says fig3
Figure 5 — GENERator BOS mediationpython experiments/figures/fig4_generator.pyexperiments/figures/main/fig4_generator.{pdf,png}⚠ script filename says fig4; companion panel from fig4_generator_specificity.py

Supplementary figures

paper objectcommandartifact
Fig S1 — structural/control detailpython experiments/figures/supplement/fig_s1_structural_detail.pyexperiments/figures/supplement/fig_s1_structural_detail.{pdf,png}
Fig S2 — damage-matched random directionpython experiments/figures/supplement/fig_s2_random_direction.pyexperiments/figures/supplement/fig_s2_random_direction.{pdf,png}

Supplementary tables

S2, S3 and S6–S8 are generated; S1, S4 and S5 are reformatted verbatim from the audit and are not rebuilt. One command produces all five generated tables.

python scripts/census_analysis/build_supplementary_tables.py
tableartifactrows
S1 — model panel and provenanceresults/supplementary/S1_model_panel_provenance.{tsv,md,csv}22
S2 — structural metrics + 24-input stabilityresults/supplementary/S2_structural_metrics_stability.{tsv,md}22
S3 — causal census + disagreement coordinatesresults/supplementary/S3_causal_census_disagreements.{tsv,md}49
S4 — structure–function correlationsresults/supplementary/S4_structure_function_correlations.{tsv,md,csv}16
S5 — GENERator conditionsresults/supplementary/S5_generator_conditions.{tsv,md,csv}106
S6 — DNABERT-2 tomographyresults/supplementary/S6_dnabert2_tomography.{tsv,md}98
S7 — within-layer sweepresults/supplementary/S7_within_layer_sweep.{tsv,md}72
S8 — two critical rows + geometryresults/supplementary/S8_two_critical_rows.{tsv,md}13

Results in the text, not in a figure

claimcommandartifact
Two critical rows in one layer, and the masking interactionpython scripts/within_layer_sweep/run_smollm2_second_row_epistasis.pyresults/analyses/within_layer_sweep/smollm2_second_row_epistasis.json
Row geometry against a same-layer null (data-free, no GPU)python scripts/within_layer_sweep/run_smollm2_row_geometry.pyresults/analyses/within_layer_sweep/smollm2_161_749_geometry.json
Selection-rule resolution for every legacy candidatebash pipelines/detector_provenance.shresults/analyses/detector_provenance/EXP2_LEGACY_DETECTOR_RESOLUTION.md
Cohort structure–function correlationspython scripts/census_analysis/run_activation_vs_causality.pyresults/analyses/census_analysis/activation_vs_causality.tsv

The authoritative, machine-checked mapping is docs/EXPERIMENT_MAP.md (21 experiments) and, panel by panel, experiments/figures/FIGURE_PROVENANCE.md. This table surfaces them; it does not replace them. python scripts/build_experiment_map.py re-verifies that every script and artifact named there still exists.

Running the pipelines

Prefer the pipelines. Each skips stages whose output already exists, so an interrupted run resumes and a finished one costs nothing; FORCE=1 recomputes.

bash pipelines/census.sh                 # the preregistered 22-model causal census (restartable)
bash pipelines/census.sh dnabert2 ntv3   # ...or a subset
bash pipelines/detector_provenance.sh    # selection-rule resolution; runs its positive control first
bash pipelines/fig5_within_layer.sh      # the within-layer sweeps and second critical row
                                         # (filename retains an earlier figure number)

Individual stages:

# structural panel and causal census
python experiments/E11_scale_ladder/run_model.py --model <slug>
python experiments/E13_full_cohort_causal_census/run_singleton_census.py --model <slug>

# mechanism case studies
python experiments/E9_mechanistic_tomography/run_fit_observers.py
python experiments/E12_generator_degradation_control/run_bos_mediation_main.py

# within-layer sweeps
python scripts/within_layer_sweep/run_within_model_slope_text.py     # SmolLM2-1.7B, ~7 min, 1 GPU
python scripts/within_layer_sweep/run_smollm2_row_geometry.py        # data-free, no GPU

# supplementary tables S2, S3, S6-S8 (rebuilt from committed artifacts)
python scripts/census_analysis/build_supplementary_tables.py

# two flags that are REQUIRED and silently wrong if omitted
python scripts/detection/run_detection.py --model ntv3 --pad_to_multiple 256   # stride-256 U-Net
python scripts/evaluation/run_gue_multiseed.py --model ntv3 --max_length 400   # nucleotide tokenizer

Verify the repository's own invariants:

python scripts/build_experiment_map.py    # every claim's code and artifacts exist
python src/prereg_lock.py verify --all    # 12 preregistrations, content-locked
pytest tests/                             # unit tests + every CLI entry point starts

Repository map

experiments/ contains the preregistered harnesses (E1–E13, each with the preregistration it was run under in docs/prereg/); scripts/ contains analyses developed after preregistration. The split is deliberate: it lets a reader see at a glance which analyses were locked in advance and which came later.

pathcontents
experiments/E1–E13The preregistered harnesses, one directory per experiment line. Not edited after the fact to make later results come out differently. E5_dimensionality/ is a cut line whose library is still imported by three audit builders — see its README.
experiments/figures/Figure render scripts, output, source_data/ (the exact plotted values), and FIGURE_PROVENANCE.md
scripts/detection/Super-row detection and selection-rule resolution
scripts/mechanism/BOS mediation, attention sink, special-token dependence, matched replacements
scripts/within_layer_sweep/The graded within-layer sweeps, the second critical row, Figure 5
scripts/census_analysis/Cohort structure–function correlations; the supplementary-table builder
scripts/negative_results/Experiments whose only result is a null — see its README
scripts/evaluation/GUE downstream evaluation
pipelines/Reproduction runners
src/Shared library: activation capture, ablation, spike detection, DNA probes, the prereg lock
models/, configs/Per-model wrappers and YAML, loaded dynamically via WRAPPER_MAP
stubs/Import shims, not PEP 484 type stubs — they let wrappers for models outside the paper's panel import without heavy optional dependencies. See stubs/README.md.
audit/The verification record: census_master.csv (22 models × 44 columns) is the canonical table. Three adversarial passes; see its README.
results/Artifacts in four groups — experiments/ (per harness), analyses/ (derived), negative_results/, supplementary/ (S1–S8). Gitignored by default; files backing a reported number are force-added. See its README.
docs/The experiment map and the 12 locked preregistrations
frozen_inputs/, data/, tests/Content-hashed inputs, small reference files, tests

Provenance and known limitations

Stated plainly, because a reader will find them anyway.

  1. Some raw artifacts are not committed. Several were produced on a cluster and never transferred. For every affected item the committed figure source-data snapshot under experiments/figures/source_data/ carries the plotted values, so each reported number remains inspectable.
  2. NTv3's original weight revision was not recorded and is not recoverable. Resolved Hub commits exist for 21 of 22 models.
  3. One n=10 subgroup is fragile. The text-decoder correlation moves from ρ=0.770 to 0.673 under an OLMo coordinate substitution, with a 95% lower bound of +0.032. It should not be read as independently robust; the 22-model result is insensitive to the substitution.
  4. Experiment lines that the paper does not report are not in the working tree. Their preregistrations are retained in docs/prereg/, each with an explicit disposition, rather than deleted — see docs/prereg/README.md. E5_dimensionality/ keeps one file, a library three audit builders import.
  5. The preregistrations record what was planned, including paths that predate later directory renames. They are content-locked and were deliberately never rewritten to match.

Citation

See CITATION.cff. Released under the MIT License (LICENSE).

Prior work this builds on: Yu M, Wang D, Shan Q, Reed CJ, Wan A. The Super Weight in Large Language Models. arXiv:2411.07191 (2024).