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MLP on summed gene embeddings, trained once on a downsampled set

MLP on summed gene embeddings trained once on a subsample of measured pairs to predict the viability of held-out pairs.

1 evaluation · 12 results

Overview

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Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

Evaluations and results

1 evaluation · 12 results. Different protocols are not a single leaderboard.

Protocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency

Sorted by RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average) (lower is better). The best value in each column is highlighted. Decimals are rounded for display; each value links to the printed value and its source.

All 12 result rows with coverage, uncertainty and sources
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Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)
3.5 (1.0) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average)
unitless · lower

Uncertainty: SE 1.0. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "MLP", column "Horlbeck Jurkat"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)
3.0 (0.4) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average)
unitless · lower

Uncertainty: SE 0.4. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "MLP", column "Horlbeck Jurkat"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in Jurkat T cells, gene-level viability (as processed by Qin et al. 2025)
5.5 (2.1) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average)
unitless · lower

Uncertainty: SE 2.1. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck Jurkat (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "MLP", column "Horlbeck Jurkat"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
6.3 (1.1) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average)
unitless · lower

Uncertainty: SE 1.1. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "MLP", column "Horlbeck K562"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
5.9 (0.1) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average)
unitless · lower

Uncertainty: SE 0.1. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "MLP", column "Horlbeck K562"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Horlbeck et al. 2018 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
7.8 (2.5) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average)
unitless · lower

Uncertainty: SE 2.5. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Horlbeck K562 (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "MLP", column "Horlbeck K562"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)
5.7 (1.3) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average)
unitless · lower

Uncertainty: SE 1.3. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "MLP", column "Norman"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)
5.0 (1.4) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average)
unitless · lower

Uncertainty: SE 1.4. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "MLP", column "Norman"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Norman et al. 2019 combinatorial CRISPRa in K562, gene-level viability (as processed by Qin et al. 2025)
7.7 (0.9) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average)
unitless · lower

Uncertainty: SE 0.9. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Norman (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "MLP", column "Norman"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
2.4 (0.4) RMSE (test RMSE of pair viability, training set with each gene seen about 10 times on average)
unitless · lower

Uncertainty: SE 0.4. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 6, Gene Frequency 10 block, row "MLP", column "Simpson"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
2.0 (0.3) RMSE (test RMSE of pair viability, training set with each gene seen about 20 times on average)
unitless · lower

Uncertainty: SE 0.3. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 20 block, row "MLP", column "Simpson"
Configuration: MLP on summed gene embeddings, trained once on a downsampled setProtocol: Combination phenotype prediction from small training sets: test RMSE at fixed average gene frequency
Dataset: Simpson et al. 2023 combinatorial CRISPRi in K562, gene-level viability (as processed by Qin et al. 2025)
4.3 (0.9) RMSE (test RMSE of pair viability, training set with each gene seen about 4 times on average)
unitless · lower

Uncertainty: SE 0.9. Caption: error is SE across three cross-fold replicates

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

MLP on summed gene embeddings, trained once on a downsampled set on Simpson (Tables 1 and 6, RMSE at fixed gene frequency)

pheno-20261022-qin2025-protocol-downsampling-rmse

Aggregation: Not reported

Qin et al. 2025, Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations (ICML 2025, PMLR 267) · Table 1, Gene Frequency 4 block, row "MLP", column "Simpson"

Source checking is not independent reproduction. Release 2026-10-23-5347695500ed.

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

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Technical metadata and extraction receipts

Stable ID: pheno-20261022-qin2025-config-mlp-gene-embedding-prediction

areas
cells-tissues
contexts
research
method types
supervised_machine_learning
reported name
MLP
configuration type
reported_configuration
foundation model eligible
false
version
As run by Qin et al. 2025 (PMLR 267); no release or commit is printed
access reuse
Run by Qin et al. 2025; their code for this comparator is not separately identified
parameters
128-dimensional gene embeddings summed and projected to one value; learning rate 0.01, batch size 1024, linear schedule with 10% warm-up, weight decay 0 (Appendix B, F).
source locator
Table 1 and Table 6, row 'MLP'; Appendix B
provenance note
Configuration run by Qin et al. 2025 in this comparison.
review
method: source-hash-verification; scope-review; reviewer: claude; reviewer note: Claude (Opus 5.5) review agent, independent of the extraction agent; no human review claimed; date: 2026-10-22; artifact sha256: 983b2da8aed78f0aced27053301c15f0f67ebd0fac706435bb6800e309dd64eb; retrieval url: https://raw.githubusercontent.com/mlresearch/v267/main/assets/qin25g/qin25g.pdf; method note: Re-hashed the PDF in the scratchpad (SHA-256 matches the source record). Read the cited sections in the pdftotext layer of the pinned PDF.; note: Fields checked against the cited locator; nothing found that the source does not state.
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