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MechPert: Mechanistic Consensus as an Inductive Bias for Unseen Perturbation Prediction

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Predicting transcriptional responses to unseen genetic perturbations is essential for understanding gene regulation and prioritizing large-scale perturbation experiments. Existing approaches either rely on static, potentially incomplete knowledge graphs, or prompt language models for functionally similar genes, retrieving associations shaped by symmetric co-occurrence in scientific text rather than directed regulatory logic. We introduce MechPert, a lightweight framework that encourages LLM agents to generate directed regulatory hypotheses rather than relying solely on functional similarity. Multiple agents independently propose candidate regulators with associated confidence scores; these are aggregated through a consensus mechanism that filters spurious associations, producing weighted neighborhoods for downstream prediction. We evaluate MechPert on Perturb-seq benchmarks across four human cell lines. For perturbation prediction in low-data regimes ($N=50$ observed perturbations), MechPert improves Pearson correlation by up to 10.5\% over similarity-based baselines. For experimental design, MechPert-selected anchor genes outperform standard network centrality heuristics by up to 46\% in well-characterized cell lines.

Marc Boubnovski Martell, Josefa Lia Stoisser, Lawrence Phillips, Aditya Misra, Robert Kitchen, Jesper Ferkinghoff-Borg, Jialin Yu, Philip Torr, Kaspar M\"arten• 2026

Related benchmarks

TaskDatasetResultRank
Few-Shot GeneralizationK562, RPE1, Jurkat, HepG2 pooled cell lines
C20 Correlation0.62
15
Global genome predictionK562 cell line
Pearson Correlation0.536
4
Global genome predictionRPE1 cell line
Pearson Correlation Coefficient0.614
4
Global genome predictionJurkat cell line
Pearson Correlation Coefficient0.26
4
Global genome predictionHepG2 cell line
Pearson Correlation (PCC)0.181
4
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