rewirebio.iobenchmarks

Use caseCells and tissuesResearch only

Select perturbations for a defined cellular response

Which genetic perturbations should I test to produce a defined cellular response?

What the evidence shows

The evidence comes from one prospective challenge and two retrospective replays, which measure different things.

In the Cancer Immunotherapy Data Science Challenge, scored prospectively in mouse T cells, the 20 original Challenge 2 submissions had a top-k overlap AUC of 0.452 to 0.566, with 17 of the 20 between 0.50 and 0.57; a random ordering is expected to score 0.5. That score is not a ROC AUC, and the genes it scores were drawn from the leading Challenge 1 nominations. In the follow-up, two nominated targets exceeded the Screen 1 targets on the immune checkpoint blockade objective; the source reports 61 nominations, 57 selected targets, 59 screen-2 genes and 50 perturbations passing quality control without reconciling them, so no success fraction follows.

AssayBench-Loop replays 20 genome-wide CRISPR screens published after 2021, with each policy choosing 10 rounds of 100 genes. One random draw found 4.9% of each screen's hits on average (enrichment 1.04 over the random expectation). Language models used directly as the policy, with hit labels, reached enrichment of 1.39 to 4.81, BPMF 4.49, and the authors' handoffs from a language model to their AssayFormer up to 5.67, with the Gemini-3.1-Pro handoff finding 27.7% of hits.

Many recovered hits are common-essential genes: 30.1% for that handoff, 18.6% for the random draw and 99.1% for a baseline that picks earlier screens' hits. Test screens were kept only if the best language model already passed a performance floor on them, and the paper does not say whether the models saw the screens' publications in training. The authors ran every row, and no uncertainty is printed.

For two-gene combinations, NAIAD's replay of four viability screens counted how many of each screen's 200 strongest pairs the model ranked in its top 200 after four rounds: 143.0, 141.7, 99.7 and 150.0 when it acquired the pairs with the largest predicted effect, against 93.3, 70.3, 38.7 and 81.3 when it acquired pairs uniformly at random (means of three replicates). That count includes pairs the model predicted but never measured, and the uniform arm still uses the model's ranking, so it is not the yield of testing random pairs. The challenge's submissions scored close to a random ordering, while in both replays the leading model-guided policies scored above the random or uniform arm; the two differ in endpoint, candidate set, setting and who ran them, so their results cannot be compared directly.

No source compares a model shortlist with random selection prospectively at the same budget.

You bring
  • A defined cell system, starting state and target phenotype
  • Candidate genetic perturbations and a fixed testing budget
  • Measured perturbations and matched controls with guide, replicate and condition metadata
  • The intended transfer setting: unseen genes, combinations or a new cellular context
You want
A ranked experimental shortlist with predicted phenotype effects, coverage and uncertainty about unmeasured conditions.
Evidence in this release
4 comparisons shown · 47 tools · 100 configurations
Kept up to date
Evidence last checked 22 October 2026 · re-checked monthly, next due 22 November 2026

Baseline

Random selection. There is no pre-machine-learning method for choosing perturbations to reach a defined cell state, so the reference is random selection from the candidate set. Among the evidence linked to this use case, only the retrospective AssayBench-Loop replay scores it, as one random draw on the same screens and budget as the other policies; the CPPC protocols measure submitted methods only, and the challenge's ranking metric only takes 0.5 as the value expected from a random ranking. NAIAD's uniform arm still ranks pairs with the model, so it is not this baseline.

Machine-learning methods are compared with the baseline on the same data in one table: AssayBench-Loop adaptive hit discovery: 10 rounds of 100 genes on 20 held-out CRISPR screens. Baseline rows are marked in each table.

Tools compared

Comparisons

Each table is one study or protocol with its own truth set and scoring. Compare tools within a table, not across tables.

CPPC original Challenge 2 prospective target ranking score

Direct evidenceAuthor-reported

Prospective target ranking: custom top-k overlap AUC under source-defined objective and filtering aggregation.

Sorted by CPPC top-k overlap AUC (higher is better). Showing the top 10 of 20 rows. The best value in each column is highlighted.

Show all 20 rowsShow the top 10 rows only
Caveats and method
  • Custom ranking AUC is not ROC AUC, prospective hit rate or efficacy.
  • Original model implementations/checkpoints are not pinned in the intake; no uncertainty printed.
  • Automated source review only; independent human scientific review remains outstanding.

Protocol: CPPC original Challenge 2 prospective target ranking score

AssayBench-Loop adaptive hit discovery: 10 rounds of 100 genes on 20 held-out CRISPR screens

Proxy evidenceAuthor-reportedIndependent study

Hit enrichment factor over the random expectation, fraction of each screen's hits found, normalised cumulative-hit AUC, shortfall and share of common-essential hits after 10 rounds of 100 genes, mean over 20 genome-wide CRISPR screens published after 2021, for 53 configurations: one random draw, a prior-hit baseline, Screen-kNN, random forests, third-party adaptive design methods (BPMF, MAML, BioBO, Probability-of-Hit, Transformer + DAgger), language models used directly with and without hit labels, agent harnesses, and the authors' AssayFormer, AssayLLM and AssayLoop handoffs

Sorted by Effective number of groups (direction not stated). Showing the top 10 of 53 rows. The best value in each column is highlighted.

Scroll sideways to see all 10 columns.

ToolEffective number of groups (EP-B: Hill number of order 1 at batch scope, rarefied to 30 annotated genes per batch, one random group per gene per draw, 400 Monte Carlo draws, averaged within each screen then across the 20 test screens; not comparable with EP-S or EP-D)Effective number of groups (EP-D: Hill number of order 1 at dataset scope, rarefied to 6,000 annotated genes across the complete test set, one random group per gene per draw, 300 Monte Carlo draws; not comparable with EP-B or EP-S)Effective number of groups (EP-S: Hill number of order 1 at screen scope, rarefied to 200 annotated genes per screen, one random group per gene per draw, 400 Monte Carlo draws, averaged across the 20 test screens; not comparable with EP-B or EP-D)Annotation overlap ratio (mean pairwise Jaccard overlap of GO biological-process annotations within a batch, divided by that of an equal-size random batch from the screen library, averaged over batches; mean over the 20 AssayBench-Loop test screens)Hit enrichment factor (hits found divided by hits expected under random selection, after 10 rounds of 100 genes; hallucinated genes and unfilled slots count in the denominator, valid genes outside the screen library do not; mean over the 20 AssayBench-Loop test screens)Normalized cumulative hits AUC (area under the fraction-of-hits against fraction-of-library-queried curve over 10 rounds, divided by an oracle's area over the same effective budget; mean over the 20 AssayBench-Loop test screens)Proportion (share of acquired hits that are DepMap common-essential genes (1,827 genes); mean over the 20 AssayBench-Loop test screens)Proportion (shortfall: share of acquired genes outside the screen library, including hallucinated gene names; mean over the 20 AssayBench-Loop test screens)Recall (fraction of the screen's hits acquired within 10 rounds of 100 genes (FH); mean over the 20 AssayBench-Loop test screens)Vendi ratio (Vendi score of each batch under a cosine kernel on GenePT embeddings, divided by batch size and averaged over batches; mean over the 20 AssayBench-Loop test screens)
RandomBaselineconventional21.782.656.91.101.043.418.6%10.0%4.9%58.5
LLMNN [17]foundation model20.378.652.11.442.399.422.6%0.1% (best in column)12.5%64.9
Probability-of-hit [40]machine learning20.379.053.42.112.417.335.2%9.0%11.8%56.6
AssayFormer (MF)specialist model20.269.250.02.943.018.926.1%36.3%10.3%34.6
BPMF [41]machine learning20.172.550.72.054.4912.336.1%18.0%19.7%53.4
AssayFormer (MF-Sphere)specialist model20.067.548.92.763.7211.133.4%35.9%13.0%30.8
BioBO [27]machine learning19.972.650.61.682.595.938.4%10.3%12.2%64.3
Random + GRPOspecialist model19.960.846.31.992.719.871.0%10.9%12.7%54.9
AssayFormer (K562-PCA)specialist model19.864.548.42.162.9510.255.3%10.6%14.0%58.7
MAML (w/ BPMF embs.) [12, 41]machine learning19.457.844.42.543.7714.374.9%6.4%18.6%58.2
SVD + GRPOspecialist model19.464.646.62.094.4016.036.5%1.8%22.9%63.4
+ GRPO (= AssayFormer); BPMF + GRPOspecialist model19.365.046.72.384.8317.240.7%10.0%23.2%55.9
AssayFormer (SVD)specialist model19.061.145.54.623.7210.344.1%46.5%11.1%24.7
BPMF + GRPO (EFterminal)specialist model19.062.745.02.354.2914.948.4%10.7%20.5%54.2
Transformer + DAgger [39]machine learning19.053.941.92.522.8010.390.0%2.5%14.4%59.8
Handoff-trained AssayLLM → AssayFormerfoundation model, specialist model18.968.347.02.915.2318.739.2%9.1%25.1%53.7
ICBR-EF [51]foundation model18.968.544.12.322.769.332.2%0.9%14.5%61.5
Screen-kNNconventional18.954.842.82.913.4012.577.1%3.7%17.3%57.6
- screen desc. (under AssayFormer (BPMF))specialist model18.856.543.22.683.8213.162.6%5.1%19.1%56.7
AssayLLM → AssayFormerfoundation model, specialist model18.870.847.52.975.0518.634.8%7.8%24.7%55.5
GLM-5.1 → AssayFormerfoundation model, specialist model18.871.047.52.885.2719.831.6%8.5%25.5%55.9
MF-Sphere + GRPOspecialist model18.863.345.02.274.3114.639.0%11.7%20.4%52.4
BPMF (no desc.) + GRPOspecialist model18.763.145.72.554.5216.242.5%5.9%22.4%57.7
Haiku-4.5 Agentfoundation model18.668.347.32.943.2014.349.8%20.6%16.8%61.7
AssayFormer (GenePT-PCA)specialist model18.554.444.75.551.064.222.7%15.4%4.7%33.9
AssayFormer (random embs.); AssayFormer (Random)specialist model18.551.540.02.682.479.286.1%5.4%12.3%56.9
Gemini-3.1-Pro → AssayFormerfoundation model, specialist model18.470.446.63.065.67 (best in column)21.7 (best in column)30.1%7.6%27.7% (best in column)55.6
RF (greedy)machine learning18.477.349.23.241.996.430.5%3.7%9.9%50.1
+ BPMF Embeddings; AssayFormer (BPMF)specialist model18.356.942.72.543.8313.237.5%10.2%18.3%52.5
GPT-5.6 Sol → AssayFormerfoundation model, specialist model18.169.845.93.065.67 (best in column)21.7 (best in column)29.4%7.8%27.6%55.8
K562-PCA + GRPOspecialist model18.154.241.73.793.1511.679.1%6.5%15.7%55.8
RF + UCBmachine learning18.174.047.82.421.323.823.9%10.9%6.2%47.1
GPT-5.5 → AssayFormerfoundation model, specialist model17.869.645.43.285.5120.629.5%7.9%26.8%54.7
Prior hit baselineconventional17.848.438.43.222.8711.599.1%1.5%14.9%56.5
MF + GRPOspecialist model17.352.838.73.124.0513.846.5%15.8%18.9%45.5
GenePT-PCA + GRPOspecialist model16.145.035.411.462.609.373.9%10.4%12.2%38.1
- hit labels (Qwen3.6-27B)foundation model14.668.438.15.042.3210.031.2%22.6%12.1%43.5
Gemini-3.1-Profoundation model14.666.234.64.394.7120.630.6%3.6%24.6%47.4
- hit labels (Kimi-K2.6)foundation model14.562.332.94.962.7213.031.4%37.1%14.3%56.9
w/o labels (GLM-5.1)foundation model14.464.633.44.443.6515.027.6%7.3%19.1%47.0
Qwen3.6-27B; Qwen3.6-27B (base)foundation model14.368.937.54.972.6510.530.9%23.4%13.9%41.7
w/o labels (Gemini-3.1-Pro)foundation model14.363.534.34.534.3818.529.5%3.1%22.9%47.1
Claude Sonnet-4.6foundation model14.165.134.45.343.0613.329.0%29.7%16.0%51.2
GLM-5.2foundation model14.064.634.04.624.0916.629.1%5.3%21.4%47.6
+ SFT + GRPO (= AssayLLM)foundation model13.764.834.75.523.6915.537.8%16.7%19.3%41.4
+ SFT (GLM-5.1 traces)foundation model13.664.134.35.363.5614.735.9%19.0%18.7%42.2
GLM-5.1foundation model13.364.030.84.724.0016.328.9%10.6%21.0%47.2
GPT-5.6 Solfoundation model13.261.829.54.544.8120.529.6%5.0%25.2%49.7
Kimi-K2.6foundation model13.264.329.66.523.0014.131.2%54.2%15.7%60.5
- hit labels (Claude Opus-4.8)foundation model12.662.630.06.213.5515.825.8%28.9%18.6%45.4
Claude Haiku-4.5foundation model12.563.532.76.751.398.528.9%61.8%7.3%41.9
Claude Opus-4.8foundation model12.360.727.46.623.8617.328.3%35.1%20.2%48.5
GPT-5.5foundation model12.260.228.25.024.4318.727.2%5.1%23.1%46.6
Show all 53 rowsShow the top 10 rows only
Caveats and method
  • Retrospective: labels are historical screen calls, and the authors state the policies remain to be validated prospectively in a live experimental loop.
  • 20 test screens and means only: Table 1 and Supplementary Table 4 print no uncertainty, and the number of runs per row is unreported.
  • Test screens were filtered for genome-wide coverage, at least 50 hits, hit rate below 15% and a best-LLM AnDCG@100 of at least 0.05, which favours screens whose hits a language model can name; the authors say the benchmark is not an unbiased sample of genome-wide CRISPR screens.
  • The temporal split is relative to the 1,349 training screens; the paper does not say whether the test screens or their publications predate the language models' training data.
  • Many recovered hits are DepMap common-essential genes (18.6% for the random draw, 99.1% for the prior-hit baseline), so part of any enrichment can reflect generic fitness genes rather than the screen's specific phenotype.
  • Author-run: AssayFormer, AssayLLM and AssayLoop are the authors' methods, and the authors also ran every comparator; third-party rows are the authors' runs, not those methods' own published results.
  • The random policy's sampling universe (the shared gene pool or each screen's library) is not stated.
  • Preprint (arXiv v1), not peer reviewed.

Protocol: AssayBench-Loop adaptive hit discovery: 10 rounds of 100 genes on 20 held-out CRISPR screens

Retrospective active learning on a fully measured two-gene CRISPR viability screen: top-200 gene pairs found by round 4

Proxy evidenceAuthor-reportedIndependent study

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

Sorted by True positives (higher is better). Showing the top 10 of 26 rows. The best value in each column is highlighted.

Scroll sideways to see all 6 columns.

ToolTrue positives (the screen's 200 strongest measured gene pairs found among the 200 strongest measured-plus-predicted values, round 0 of active learning)True positives (the screen's 200 strongest measured gene pairs found among the 200 strongest measured-plus-predicted values, round 1 of active learning)True positives (the screen's 200 strongest measured gene pairs found among the 200 strongest measured-plus-predicted values, round 2 of active learning)True positives (the screen's 200 strongest measured gene pairs found among the 200 strongest measured-plus-predicted values, round 3 of active learning)True positives (the screen's 200 strongest measured gene pairs found among the 200 strongest measured-plus-predicted values, round 4 of active learning)Count (marginal gain (P_4 - P_0)/4 in the screen's 200 strongest measured gene pairs found, round 0 to round 4)
NAIAD, MPEmachine learning86.0 (1.0) (best in column)100.3 (0.9)112.3 (1.7) (best in column)128.0 (2.5) (best in column)143.0 (1.5)27.00 (best in column)
NAIAD, Uniformmachine learning86.0 (1.0) (best in column)88.3 (2.0)88.3 (0.3)89.7 (1.2)69.0 (1.1)7.50
RECOVER, MPEmachine learning82.0 (1.0)101.0 (1.2) (best in column)110.7 (2.0)125.0 (2.5)138.7 (2.7)Not reported
GEARS, MPEspecialist model42.0 (2.1)80.0 (1.5)91.7 (0.7)99.7 (0.3)109.3 (1.5)Not reported
NAIAD, Mean-UCB, β = 0machine learningNot reportedNot reportedNot reportedNot reported145.7 (3.8)Not reported
NAIAD, Mean-UCB, β = 0.25machine learningNot reportedNot reportedNot reportedNot reported144.7 (3.7)Not reported
NAIAD, Mean-UCB, β = 0.5machine learningNot reportedNot reportedNot reportedNot reported148.0 (2.6)Not reported
NAIAD, Mean-UCB, β = 0.75machine learningNot reportedNot reportedNot reportedNot reported147.3 (2.0)Not reported
NAIAD, Mean-UCB, β = 1machine learningNot reportedNot reportedNot reportedNot reported144.7 (2.6)Not reported
NAIAD, Mean-UCB, β = 1.5machine learningNot reportedNot reportedNot reportedNot reported144.3 (2.3)Not reported
NAIAD, Mean-UCB, β = 10machine learningNot reportedNot reportedNot reportedNot reported142.3 (2.6)Not reported
NAIAD, Mean-UCB, β = 2machine learningNot reportedNot reportedNot reportedNot reported144.0 (3.6)Not reported
NAIAD, Mean-UCB, β = 25machine learningNot reportedNot reportedNot reportedNot reported124.0 (4.5)Not reported
NAIAD, Mean-UCB, β = 5machine learningNot reportedNot reportedNot reportedNot reported144.0 (2.6)Not reported
NAIAD, MPE, ensemble size 1machine learningNot reportedNot reportedNot reportedNot reported149.7 (2.7) (best in column)Not reported
NAIAD, MPE, ensemble size 3machine learningNot reportedNot reportedNot reportedNot reported146.3 (3.8)Not reported
NAIAD, MPE, ensemble size 5machine learningNot reportedNot reportedNot reportedNot reported143.3 (2.6)Not reported
NAIAD, MPE, ensemble size 7machine learningNot reportedNot reportedNot reportedNot reported143.3 (3.0)Not reported
NAIAD, UCBmachine learningNot reportedNot reportedNot reportedNot reported102.7 (8.1)18.75
NAIAD, Uncertaintymachine learningNot reportedNot reportedNot reportedNot reported74.09.50
NAIAD, Uniform, ensemble size 1machine learningNot reportedNot reportedNot reportedNot reported66.7 (4.7)Not reported
NAIAD, Uniform, ensemble size 3machine learningNot reportedNot reportedNot reportedNot reported67.7 (4.6)Not reported
NAIAD, Uniform, ensemble size 5machine learningNot reportedNot reportedNot reportedNot reported68.0 (2.6)Not reported
NAIAD, Uniform, ensemble size 7machine learningNot reportedNot reportedNot reportedNot reported71.3 (4.4)Not reported
RECOVER, UCBmachine learningNot reportedNot reportedNot reportedNot reported62.0 (14.1)Not reported
RECOVER, Uniformmachine learningNot reportedNot reportedNot reportedNot reported44.3 (0.3)Not reported
Show all 26 rowsShow the top 10 rows only

The value after ± or in brackets is a standard error.

Caveats and method
  • 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.

Protocol: Retrospective active learning on a fully measured two-gene CRISPR viability screen: top-200 gene pairs found by round 4

CPPC prospective nomination of desired T-cell states

Direct evidenceAuthor-reported

Prospective nomination campaign: count of named targets improving the defined T-cell state objective.

Single reported result.

CPPC submitted-method nomination campaign

Count (nominated targets reaching desired state)
two
Caveats and method
  • No matched-budget conventional/random prospective comparison; no antitumor efficacy, rescue or selectivity result in this endpoint.
  • 61 nominations / Results 57 selected targets / README 59 targets / 50 post-QC perturbations need reconciliation; no success fraction calculated.
  • Preprint v1; original and reimplemented ranking scores kept separate. Screen2 ranking population is enriched by original nomination methods.
  • Automated source review only; independent human scientific review remains outstanding.

Protocol: CPPC prospective nomination of desired T-cell states

Not covered yet

  • 61 nominations / Results 57 selected targets / README 59 targets / 50 post-QC perturbations need reconciliation; no success fraction calculated.
  • Automated source review only; independent human scientific review remains outstanding.
  • Custom ranking AUC is not ROC AUC, prospective hit rate or efficacy.
  • No matched-budget conventional/random prospective comparison; no antitumor efficacy, rescue or selectivity result in this endpoint.
  • Original model implementations/checkpoints are not pinned in the intake; no uncertainty printed.
  • Preprint v1; original and reimplemented ranking scores kept separate. Screen2 ranking population is enriched by original nomination methods.
  • Matched random comparisons are retrospective only. AssayBench-Loop replays 20 screens with one random draw and prints no uncertainty; NAIAD's uniform arm still ranks pairs with the model, so the yield of testing randomly chosen pairs is not reported.
  • No prospective comparison of a model shortlist against random or conventional selection at the same budget.
  • The retrospective comparisons (AssayBench-Loop, NAIAD) were run by the developers of one of the compared methods; no independent replication.
  • Retrospective hits are each screen's own significance call. In AssayBench-Loop many recovered hits are common-essential genes, and the paper does not address whether the language models saw the test screens' publications in pre-training.
  • Combination evidence covers four two-gene viability screens only, gives the model every single-gene effect, and counts predicted as well as measured pairs as found.

Contribute evidence or propose a correction

Question, sources and review

Who this is for, setting and exclusions

Allocate a fixed experimental budget to perturbations most likely to produce the prespecified phenotype.

Who this is for
  • Functional genomics screen designers
  • Cell biologists planning perturbation experiments
Biological setting
Research selection for a defined genetic-perturbation screen. Chemical interventions and combinations need their own protocols. This question concerns phenotype hits rather than expression reconstruction alone.
Research setting
Research only. Predicted cellular responses do not establish patient response or treatment-selection validity.

Outside this use case

  • Transcriptome similarity alone does not establish successful experimental selection.
  • Generalisation to an unseen gene, combination and cell context must be evaluated separately.
  • Choosing experiments to maximise information gain is a separate decision.
Evidence collection plan
Evidence collection planCollecting evidence

Already on record: 4 comparisons shown · 47 tools, in the evaluated evidence above. The status above describes only the specific comparison in this plan, which remains open; it does not mean no evidence has been collected. The plan defines a comparison to investigate; it does not establish model performance or suitability.

Comparison question

Does a model select more perturbations producing a prespecified phenotype than simple controls at the same test budget in the intended held-out setting?

Baselines, outcomes and validation requirements

Baselines to include

  • Random candidate selection and mean-response/no-change controls
  • Linear or other simple statistical response models
  • Nearest measured perturbation

Outcomes to measure

  • Experimentally confirmed phenotype hits per test budget
  • Perturbation-specific expression signal as an intermediate endpoint
  • Coverage and uncertainty for unseen interventions or contexts

Validation requirements

  • Use the same candidate universe, phenotype definition and budget; specify how tied rankings are sampled.
  • Separate unseen genes, combinations and cell contexts, holding out biological and experimental units.
  • Audit guide efficacy, shared controls, batch effects and model training overlap.
  • Do not choose evaluation genes using held-out responses; keep information-gain design separate.

Next collection task

Find or commission a prospective comparison of a model shortlist against random selection from the same candidate universe at the same budget, and a retrospective comparison run by someone other than the methods' developers. The 22 October 2026 pass found matched random comparisons only in retrospective replays (AssayBench-Loop, NAIAD). Obtain qualified scientific review.

Related articles
Sources, review and downloads

Automated source review · 2026-09-30 · Codex source curation, independent worker cross-review and root integration review

Source-backed literature curation with independent automated transcription and scope checks. No new model execution, independent experimental replication, qualified human scientific review or clinical validation.

Release 2026-11-02-a7f03c9e55a5 · question use-case-phenotype-perturbation-selection

Use-case input digest 43a80aef5473f1a49c013b6d46b720b850ff5a0d18dcbb741dcdeed1ed082db1

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