rewire.itbenchmarks
Task

transcription-factor DNA binding-site prediction

Transcription-factor binding classification evaluates many TF–cell-type labels on chromosome-held-out genomic sequences.

SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

6 evaluations · 12 results

Overview

Datasets

EPBDXDNA/ENCODE ChIP-seq-derived human genomic bins with multilabel binding annotations.

Metrics

Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.

Allowed inputs

Genomic sequence bins with multilabel targets.

SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
Evaluation procedure diagram
How it worksComputational evaluation flow
Computational evaluation flow1. Input: Genomic sequence bins with multilabel targets.. Then: 2. Evaluation: Supervised binding prediction with chromosome-separated training/validation/test data.. Then: 3. Readout: Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.Computational evaluation flow1. Input: Genomic sequence bins with multilabel targets.. Then: 2. Evaluation: Supervised binding prediction with chromosome-separated training/validation/test data.. Then: 3. Readout: Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.Computational evaluation flow1. Input: Genomic sequence bins with multilabel targets.. Then: 2. Evaluation: Supervised binding prediction with chromosome-separated training/validation/test data.. Then: 3. Readout: Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.

Conceptual summary of the cited evaluation; exact task configuration and source version remain part of the protocol.

SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

limited source coverage · Automated source review, 2026-09-16. All specifications and missing details

Results

Each comparison retains its reviewed evaluation scope, dataset and metric. Results are shown without a pooled ranking.

TF-cell-type binding on held-out chromosomes8and9 · Table 2.

AUROC (fraction) · Higher values are better.

TF-cell-type binding on held-out chromosomes8and9 (transcription-factor DNA binding-site prediction) · genome-wide TF binding sites

Evidence origin: Independent external evaluation, Result quoted from another source, Author-reported evaluation.

Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Table 2.: AUROC, TF-cell-type binding on held-out chromosomes8and9
  • Chromosome separation does not itself eliminate pretraining overlap.
  • Within-paper aggregate only; do not compare against different label sets.
  • EPBDXDNABERT-2 values are quoted from its original publication because retraining code/data were unavailable; its predictions were not available for paired testing.
Comparison details and limitations

Per-label AUROC/AUPR macro-averaged over 690 labels. Same Table 2 test cohort; methods differ in additional protein/dynamics inputs. DeepSEA-derived 690 TF-cell-type labels; chr 7 validation; remaining autosomes+X training; chr 8/9 test.

  • No interval assigned unless printed in source cell.

Automated source review: 2026-09-17. Numerical source review does not establish independent reproduction.

Dots show point estimates. Whiskers show only explicitly defined uncertainty (standard deviation, standard error or a labelled interval); their definitions remain in Table. Unresolved uncertainty is not plotted. Differences do not establish statistical significance.

Showing 6 of 6 matching rows.

Methods and evaluation design

Procedure, tasks and evaluated configurations

How it works

Evaluation methodology

EPBDXDNA/ENCODE ChIP-seq-derived human genomic bins with multilabel binding annotations. Chromosomes 8/9 are held out for testing, chromosome 7 for validation and remaining specified chromosomes for training. Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments. TBiNet and EPBDXDNABERT-2 are explicit comparators; the latter’s underlying predictions were unavailable for paired statistical analysis. Chromosome-separated partitions reduce direct genomic overlap; validation data drive hyperparameter selection. Paired t-tests against TBiNet use TF–cell-type combinations as the comparison units; unavailable comparator predictions prevent the same paired analysis for every baseline.

SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Evaluation design

Benchmarks bring together tasks and protocols. A task describes the biological question; a protocol defines a particular test.

These source-backed links do not make different protocols or scores interchangeable.

Run this benchmark

Choose a concrete protocol before running an evaluation. Its inputs, split and scoring rules determine which results can be compared.

Run instructions

No runnable recipe has been reviewed for this task. Dataset access, model requirements, licences and compute requirements must be checked against its sources before execution.

A task describes a biological question. Choose a linked protocol to obtain concrete split and scoring instructions.

Strengths, limitations and unresolved questions

Strengths and limitations

Strengths and considerations

No source-reviewed explanatory claims are recorded here yet.

Profile review details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Stable record: reported-task-ac191e878dff5e

Specifications

Inputs, training, access and other details

Explanatory profile: limited source coverage · Automated source review, 2026-09-16. Review applies to the cited claims; unresolved fields are listed below. Numerical results retain their own review status.

Data, procedure and scoring
PropertyDescription and evidence
DatasetsEPBDXDNA/ENCODE ChIP-seq-derived human genomic bins with multilabel binding annotations.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
SplitsChromosomes 8/9 are held out for testing, chromosome 7 for validation and remaining specified chromosomes for training.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
MetricsPer-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
BaselinesTBiNet and EPBDXDNABERT-2 are explicit comparators; the latter’s underlying predictions were unavailable for paired statistical analysis.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
Leakage controlsChromosome-separated partitions reduce direct genomic overlap; validation data drive hyperparameter selection.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
UncertaintyPaired t-tests against TBiNet use TF–cell-type combinations as the comparison units; unavailable comparator predictions prevent the same paired analysis for every baseline.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
Entity typePaper-specific computational evaluation protocol.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
OrganismsHuman.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
AssaysENCODE ChIP-seq transcription-factor binding annotations.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
Allowed inputsGenomic sequence bins with multilabel targets.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages
AdaptationSupervised binding prediction with chromosome-separated training/validation/test data.
SourcesIntegrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction · Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Evidence

Source checking verifies the cited claim or transcription. It does not establish independent reproduction.

Papers and result coverage

Last literature check: 2026-09-17. Primary-source discovery and table/protocol screening; source checked is not independently reproduced. Raw acquisitions not automatically numerical publication approval.

Paper or primary resourceVersionReference
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site predictionversion of recordRead source
DOI: 10.1093/nargab/lqag047
Historical gaps recorded on 2026-09-17

The catalogue now holds 12 result rows for this benchmark. A note below about pending extraction describes the state on 2026-09-17 and may since have been answered by a later batch. The result rows and their sources are the current record.

  • Independent batch review before import; preserve existing observation identities.
Search and extraction details

complete comparison tables extracted pending publication review

Searches

  • Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction primary paper benchmark results

Evidence locations

  • Table2; chromosome partition Table1; Training and evaluation

Evidence table

Inspect claims, sources and review details

Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.

One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.

17 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-09-29-06401fd5b220
Property and statementOriginal source and locationReview and provenance
Diagram caption
Conceptual summary of the cited evaluation; exact task configuration and source version remain part of the protocol.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.diagram.caption

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Diagram steps
  • Input: Genomic sequence bins with multilabel targets.
  • Evaluation: Supervised binding prediction with chromosome-separated training/validation/test data.
  • Readout: Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.diagram.steps

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Diagram title
Computational evaluation flow
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.diagram.title

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Datasets
EPBDXDNA/ENCODE ChIP-seq-derived human genomic bins with multilabel binding annotations.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.0.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Splits
Chromosomes 8/9 are held out for testing, chromosome 7 for validation and remaining specified chromosomes for training.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.1.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Adaptation
Supervised binding prediction with chromosome-separated training/validation/test data.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.10.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Metrics
Per-label AUROC and AUPR are macro-averaged across TF–cell-type experiments.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.2.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Baselines
TBiNet and EPBDXDNABERT-2 are explicit comparators; the latter’s underlying predictions were unavailable for paired statistical analysis.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.3.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Leakage controls
Chromosome-separated partitions reduce direct genomic overlap; validation data drive hyperparameter selection.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.4.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Uncertainty
Paired t-tests against TBiNet use TF–cell-type combinations as the comparison units; unavailable comparator predictions prevent the same paired analysis for every baseline.
Individual claims
Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction

Original source ↗

Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages

Version: version of record
Retrieved: 2026-09-16T10:33:58.585Z

source checked

automated source review · 2026-09-16

Audit details

Task-specific computational methodology and field context checked in the cited primary-source artifact. Source-backed fields, inapplicable evaluator dimensions and unresolved details are distinguished. Numerical results were not reproduced.

Field: attributes.profile.facts.5.value

Source artifact SHA-256: 5d777f5925e941b7d087035d5d87e79ef75ae8d6456a770ffe8c527da566fee0

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Sources and history

View linked audit checks and correction history

Release 2026-09-29-06401fd5b220 · Record review: needs review

2 source records and release historyDownload this release
Technical metadata and extraction receipts

Stable ID: reported-task-ac191e878dff5e

areas
molecular-interactions
tasks
transcription-factor DNA binding-site prediction
entity level
task
version
Not reported
task
transcription-factor DNA binding-site prediction
scope note
Paper-specific evaluation task; protocol completeness requires further extraction.
comparison panels
id: part2-transbind-2026-tbl2-06294a7ed9; title: TF-cell-type binding on held-out chromosomes8and9 · Table 2.; protocol id: paper-protocol-6821afc366eb11d0c6; dataset id: reported-dataset-034c60a2dabc73; metric: AUROC; unit: fraction; direction: higher; result ids: paper-result-8e4b88567c025003ed; paper-result-5c446c8d7902f5ff2b; paper-result-1d4fe2cf1475e26a45; paper-result-ced903b7d93ba17186; paper-result-684ff8c686809c84b0; lit-b4-023; source ids: part2-transbind-2026; source locator: Table 2.: AUROC, TF-cell-type binding on held-out chromosomes8and9; context: Per-label AUROC/AUPR macro-averaged over 690 labels. Same Table 2 test cohort; methods differ in additional protein/dynamics inputs. DeepSEA-derived 690 TF-cell-type labels; chr 7 validation; remaining autosomes+X training; chr 8/9 test.; caveats: Chromosome separation does not itself eliminate pretraining overlap.; Within-paper aggregate only; do not compare against different label sets.; EPBDXDNABERT-2 values are quoted from its original publication because retraining code/data were unavailable; its predictions were not available for paired testing.; No interval assigned unless printed in source cell.; review: method: automated_source_review; date: 2026-09-17; id: part2-transbind-2026-tbl2-fe3d7b6ab2; title: TF-cell-type binding on held-out chromosomes8and9 · Table 2.; protocol id: paper-protocol-6821afc366eb11d0c6; dataset id: reported-dataset-034c60a2dabc73; metric: AUPR; unit: fraction; direction: higher; result ids: paper-result-0f2759fe5b6ccce7e1; paper-result-d386eaf35eb25ef60a; paper-result-a2922906b449e8d5c5; paper-result-ec2a592fbd35502a5b; paper-result-afd5bc7f082f6ab7e4; paper-result-1237415199f36ae278; source ids: part2-transbind-2026; source locator: Table 2.: AUPR, TF-cell-type binding on held-out chromosomes8and9; context: Per-label AUROC/AUPR macro-averaged over 690 labels. Same Table 2 test cohort; methods differ in additional protein/dynamics inputs. DeepSEA-derived 690 TF-cell-type labels; chr 7 validation; remaining autosomes+X training; chr 8/9 test.; caveats: Chromosome separation does not itself eliminate pretraining overlap.; Within-paper aggregate only; do not compare against different label sets.; EPBDXDNABERT-2 values are quoted from its original publication because retraining code/data were unavailable; its predictions were not available for paired testing.; No interval assigned unless printed in source cell.; review: method: automated_source_review; date: 2026-09-17
benchmark research
review date: 2026-09-17; status: complete_comparison_tables_extracted_pending_publication_review; primary sources: part2-transbind-2026; inspected locators: Table2; chromosome partition Table1; Training and evaluation; searched queries: Integrating protein and DNA embeddings for improving genome-wide transcription factor binding site prediction primary paper benchmark results; gaps: Independent batch review before import; preserve existing observation identities.; claim scope: Primary-source discovery and table/protocol screening; source checked is not independently reproduced. Raw acquisitions not automatically numerical publication approval.
historical missing metadata
protocol version: not_reported_in_legacy_extract
metadata review scope
historical_missing_metadata preserves the original discovery state. Current descriptive evidence and missingness are recorded in profile.facts; numerical-result review is separate.
legacy kinds
benchmark
entity classification
review date: 2026-09-17; rationale: This source-scoped record identifies the biological prediction task and holds its paper context. Preserve the existing task identity; exact split, model adaptation and scoring remain in linked evaluations or separate protocol records.; source ids: transbind-2026; source locator: Methods: DNA data; Training and evaluation; cached text lines 13–18, 49–51; comparative evaluation and ablation passages; uncertainty/repeat-run/statistical-comparison passages; ambiguities: A paper- or suite-specific task may constrain some inputs or metrics; that alone does not make it interchangeable with a complete versioned protocol. No protocol equivalence is inferred.; Some legacy profile Entity type facts use the generic phrase computational evaluation protocol. That boilerplate is not sufficient to establish a single fixed protocol identity or to merge this task with another protocol record.
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