rewirebio.iobenchmarks
Evidence claim

Relevance of Retrospective active learning on a fully measured two-gene CRISPR viability screen: top-200 gene pairs found by round 4 to "Select perturbations for a defined cellular response"

Use case
Select perturbations for a defined cellular response
Assessed by
Retrospective active learning on a fully measured two-gene CRISPR viability screen: top-200 gene pairs found by round 4
Relevance
Proxy evidence
Endpoint
Number of each screen's 200 strongest measured gene pairs that fall in the top 200 of the measured-plus-predicted ranking after four rounds of active learning (and by round, ensemble size and UCB weight), on four fully measured two-gene CRISPR viability screens (Norman, Simpson, Horlbeck K562, Horlbeck Jurkat), for NAIAD, RECOVER and GEARS under uniform, maximum-predicted-effect, UCB, uncertainty and mean-UCB acquisition

The only stored evidence on choosing which gene combinations to test: acquisition strategies compared at a fixed number of measured pairs from a shared seed set. Proxy, because the count includes strong pairs the model only predicted, the truth is the 200 largest viability effects in the same screen, and the screens are replayed rather than tested.

120 reviewed evaluations

Evidence

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

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.

16 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-23-5347695500ed
Property and statementOriginal source and locationReview and provenance
Citation locations
1 values
  • source id
    pheno-20261022-qin2025-source-pmlr
    locator
    Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.citation_locators

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Constraints
5 values
  • Cite Table 4 (three replicates with standard error) for round-4 comparisons. Table 2 and Table 3 are separate runs with no stated run count and differ from Table 4 by more than rounding.
  • Compare only within one screen; the budget and the share of pairs in the top 200 differ by screen.
  • Do not compare this count with AssayBench-Loop's fraction of hits found or with any count of tested hits.
  • Do not treat the Uniform rows as the use case's random-selection baseline.
  • Inspect every linked evaluation's source locator and limitations before citing a result.
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.constraints

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Endpoint
Number of each screen's 200 strongest measured gene pairs that fall in the top 200 of the measured-plus-predicted ranking after four rounds of active learning (and by round, ensemble size and UCB weight), on four fully measured two-gene CRISPR viability screens (Norman, Simpson, Horlbeck K562, Horlbeck Jurkat), for NAIAD, RECOVER and GEARS under uniform, maximum-predicted-effect, UCB, uncertainty and mean-UCB acquisition
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.endpoint

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Claimed field
links:assessed_by:pheno-20261022-qin2025-protocol-al-top200
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.field

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Headline metric
true-positive-count
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.headline_metric

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Limitations
7 values
  • Retrospective replay over already-measured screens; no new experiment.
  • A pair counts as found when it is in the top 200 of the measured-plus-predicted ranking, whether or not it was measured.
  • Viability phenotype only, with no significance threshold. Appendix D ranks the 'top P values' without saying whether by sign or magnitude, while MPE acquires the pairs with the highest absolute predicted effect (Appendix C).
  • Budgets differ: 500 measured pairs of 6,328 for Norman, 2,500 of 95,703 to 147,658 for the other screens.
  • The model is given every gene's single-gene effect, so combinations involving a gene with an unmeasured single effect are not covered.
  • Author-reported: NAIAD is the authors' method, and they adapted and ran RECOVER (from drugs to genes) and GEARS (on synthetic expression input).
  • At most three cross-fold replicates, which the paper does not define for active learning; Table 7 and Table 4 disagree by 0.4 on one Norman cell.
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.limitations

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Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.pins

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Rationale
The only stored evidence on choosing which gene combinations to test: acquisition strategies compared at a fixed number of measured pairs from a shared seed set. Proxy, because the count includes strong pairs the model only predicted, the truth is the 200 largest viability effects in the same screen, and the screens are replayed rather than tested. The use case's setting says combinations need their own protocol, and this is one. The uniform arm is NAIAD (or RECOVER) trained on randomly chosen pairs and still ranks every pair with the model, so it is a random-acquisition control, not the yield of testing randomly chosen pairs that the collection plan's random baseline would give.
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.rationale

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Reason
Add relevance judgement for a protocol extracted in the 2026-10-22 refresh (issue #184). Drafted by the Claude (Opus 5.5) judgement agent in the evidence-pass workflow for issue #184 (batch data/omics/use-case-refresh-phenotype-20261022); no human review claimed.
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.reason

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

Relevance
proxy
Context-only references
Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267)

Original source ↗

pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D

Version: Proceedings of the 42nd ICML, PMLR 267:50363-50383, 2025; proceedings PDF qin25g.pdf. The arXiv preprint 2411.12010 was not read.
Retrieved: 2026-10-22T13:57:27Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.relevance

Source artifact SHA-256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb

Hash scope: pdftotext -layout text layer, parsed by extract/qin2025naiad.py

Inspected artifact

How to read the evidence

Sources and history

Release 2026-10-23-5347695500ed · Record review: source checked

1 source record and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: use-case-mapping-phenotype-20261022-qin2025-al-top200

field
links:assessed_by:pheno-20261022-qin2025-protocol-al-top200
value
pheno-20261022-qin2025-protocol-al-top200
relevance
proxy
endpoint
Number of each screen's 200 strongest measured gene pairs that fall in the top 200 of the measured-plus-predicted ranking after four rounds of active learning (and by round, ensemble size and UCB weight), on four fully measured two-gene CRISPR viability screens (Norman, Simpson, Horlbeck K562, Horlbeck Jurkat), for NAIAD, RECOVER and GEARS under uniform, maximum-predicted-effect, UCB, uncertainty and mean-UCB acquisition
rationale
The only stored evidence on choosing which gene combinations to test: acquisition strategies compared at a fixed number of measured pairs from a shared seed set. Proxy, because the count includes strong pairs the model only predicted, the truth is the 200 largest viability effects in the same screen, and the screens are replayed rather than tested. The use case's setting says combinations need their own protocol, and this is one. The uniform arm is NAIAD (or RECOVER) trained on randomly chosen pairs and still ranks every pair with the model, so it is a random-acquisition control, not the yield of testing randomly chosen pairs that the collection plan's random baseline would give.
constraints
Cite Table 4 (three replicates with standard error) for round-4 comparisons. Table 2 and Table 3 are separate runs with no stated run count and differ from Table 4 by more than rounding.; Compare only within one screen; the budget and the share of pairs in the top 200 differ by screen.; Do not compare this count with AssayBench-Loop's fraction of hits found or with any count of tested hits.; Do not treat the Uniform rows as the use case's random-selection baseline.; Inspect every linked evaluation's source locator and limitations before citing a result.
limitations
Retrospective replay over already-measured screens; no new experiment.; A pair counts as found when it is in the top 200 of the measured-plus-predicted ranking, whether or not it was measured.; Viability phenotype only, with no significance threshold. Appendix D ranks the 'top P values' without saying whether by sign or magnitude, while MPE acquires the pairs with the highest absolute predicted effect (Appendix C).; Budgets differ: 500 measured pairs of 6,328 for Norman, 2,500 of 95,703 to 147,658 for the other screens.; The model is given every gene's single-gene effect, so combinations involving a gene with an unmeasured single effect are not covered.; Author-reported: NAIAD is the authors' method, and they adapted and ran RECOVER (from drugs to genes) and GEARS (on synthetic expression input).; At most three cross-fold replicates, which the paper does not define for active learning; Table 7 and Table 4 disagree by 0.4 on one Norman cell.
revision
1
reason
Add relevance judgement for a protocol extracted in the 2026-10-22 refresh (issue #184). Drafted by the Claude (Opus 5.5) judgement agent in the evidence-pass workflow for issue #184 (batch data/omics/use-case-refresh-phenotype-20261022); no human review claimed.
citation locators
source id: pheno-20261022-qin2025-source-pmlr; locator: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D
source locator
pheno-20261022-qin2025-source-pmlr: Sections 4.3 and 5.3; Table 2; Table 3; Table 4; Tables 5, 7 and 8; Appendices C and D
headline metric
true-positive-count
reviewed evaluations
pheno-20261022-qin2025-eval-table2-3-naiad-mpe-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table2-3-naiad-mpe-horlbeck2018-k562; pheno-20261022-qin2025-eval-table2-3-naiad-mpe-norman2019; pheno-20261022-qin2025-eval-table2-3-naiad-mpe-simpson2023; pheno-20261022-qin2025-eval-table2-3-naiad-ucb-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table2-3-naiad-ucb-horlbeck2018-k562; pheno-20261022-qin2025-eval-table2-3-naiad-ucb-norman2019; pheno-20261022-qin2025-eval-table2-3-naiad-ucb-simpson2023; pheno-20261022-qin2025-eval-table2-3-naiad-uncertainty-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table2-3-naiad-uncertainty-horlbeck2018-k562; pheno-20261022-qin2025-eval-table2-3-naiad-uncertainty-norman2019; pheno-20261022-qin2025-eval-table2-3-naiad-uncertainty-simpson2023; pheno-20261022-qin2025-eval-table2-3-naiad-uniform-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table2-3-naiad-uniform-horlbeck2018-k562; pheno-20261022-qin2025-eval-table2-3-naiad-uniform-norman2019; pheno-20261022-qin2025-eval-table2-3-naiad-uniform-simpson2023; pheno-20261022-qin2025-eval-table4-naiad-mpe-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-naiad-mpe-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-naiad-mpe-norman2019; pheno-20261022-qin2025-eval-table4-naiad-mpe-simpson2023; pheno-20261022-qin2025-eval-table4-naiad-ucb-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-naiad-ucb-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-naiad-ucb-norman2019; pheno-20261022-qin2025-eval-table4-naiad-ucb-simpson2023; pheno-20261022-qin2025-eval-table4-naiad-uniform-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-naiad-uniform-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-naiad-uniform-norman2019; pheno-20261022-qin2025-eval-table4-naiad-uniform-simpson2023; pheno-20261022-qin2025-eval-table4-recover-mpe-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-recover-mpe-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-recover-mpe-norman2019; pheno-20261022-qin2025-eval-table4-recover-mpe-simpson2023; pheno-20261022-qin2025-eval-table4-recover-ucb-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-recover-ucb-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-recover-ucb-norman2019; pheno-20261022-qin2025-eval-table4-recover-ucb-simpson2023; pheno-20261022-qin2025-eval-table4-recover-uniform-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table4-recover-uniform-horlbeck2018-k562; pheno-20261022-qin2025-eval-table4-recover-uniform-norman2019; pheno-20261022-qin2025-eval-table4-recover-uniform-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-1-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-1-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-1-norman2019; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-1-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-3-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-3-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-3-norman2019; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-3-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-5-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-5-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-5-norman2019; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-5-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-7-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-7-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-7-norman2019; pheno-20261022-qin2025-eval-table5-naiad-mpe-ensemble-7-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-1-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-1-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-1-norman2019; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-1-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-3-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-3-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-3-norman2019; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-3-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-5-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-5-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-5-norman2019; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-5-simpson2023; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-7-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-7-horlbeck2018-k562; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-7-norman2019; pheno-20261022-qin2025-eval-table5-naiad-uniform-ensemble-7-simpson2023; pheno-20261022-qin2025-eval-table7-gears-mpe-norman2019; pheno-20261022-qin2025-eval-table7-naiad-mpe-norman2019; pheno-20261022-qin2025-eval-table7-naiad-uniform-norman2019; pheno-20261022-qin2025-eval-table7-recover-mpe-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-25-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-25-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-25-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-25-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-5-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-5-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-5-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-5-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-75-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-75-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-75-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-75-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-0-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-5-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-5-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-5-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-5-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-1-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-10-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-10-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-10-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-10-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-2-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-2-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-2-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-2-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-25-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-25-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-25-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-25-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-5-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-5-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-5-norman2019; pheno-20261022-qin2025-eval-table8-naiad-mean-ucb-beta-5-simpson2023; pheno-20261022-qin2025-eval-table8-naiad-uniform-horlbeck2018-jurkat; pheno-20261022-qin2025-eval-table8-naiad-uniform-horlbeck2018-k562; pheno-20261022-qin2025-eval-table8-naiad-uniform-norman2019; pheno-20261022-qin2025-eval-table8-naiad-uniform-simpson2023
review
method: source-hash-verification; scope-review; ai-assisted-source-review; reviewer: claude; reviewer note: Claude (Opus 5.5) use-case review agent in the evidence-pass workflow for issue #184, independent of the agent that drafted these judgements and the summary; no human review claimed; reviewed at: 2026-10-22T18:00:00Z; note: Proxy confirmed: combination selection at a fixed number of measured pairs from a shared uniform seed set, but the count includes predicted pairs (Appendix D), the truth is the 200 strongest measured effects in the same screen, and the replay is retrospective. Uniform accepted as a random-acquisition control inside the model's pipeline (Section 5.3; Appendix C.5), not the use case's random-selection baseline. All 120 evaluations kept: Table 2/3 runs have null aggregation, which blocks automatic comparison with Table 4, and the one GEARS row carries its synthetic-input caveat. Reviewer corrected the 'strongest by magnitude' limitation, which Appendix D does not state. See docs/reviews/use-cases/phenotype-perturbation-selection-2026-10-22.md.
pins
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