cs.LGSep 23, 2026

Discover, Falsify, Revise: Auditing Input-Use Claims from Source Code to Predictive Contribution in Agent-Discovered Cell Models

Authors: Mengran LiBo LiChengyang ZhangYang YanJinfeng XuZhenchao Tang

Abstract

AI virtual cells aim to predict cellular responses to specified interventions, yet held-out predictive performance alone does not establish use of the supplied perturbation information. This prediction-claim gap matters in agentic model discovery, where language-model agents generate and revise predictors using score-based feedback. We introduce CELLAUDIT, which audits input-use claims by asking whether an input can enter the cited computation, whether fitted predictions depend on it, and whether that dependence improves prediction of observed response. On a paired morphology-transcriptomics perturbation benchmark (BBBC047), an agent-selected predictor attains a mean held-out Global Pearson correlation coefficient (PCC) of 0.3153 but remains invariant to compound replacement; a control-profile-only predictor reaches 0.3142. Source inspection identifies a compound-query pathway blocked by singleton key-value attention, and the invariance persists after refitting with disjoint control wells. In a stratified audit of 48 candidates across two linked tasks, 47 change predictions under compound replacement on both held-out folds, but only 20 show target-loss gains with intervals above zero on both folds. On BBBC047, falsification-guided revisions recover positive mean compound contributions while retaining gains over the control-profile-only baseline. In matched sci-Plex searches, audit-enriched feedback yields higher held-out performance and larger mean compound and dose contributions across five trajectories, although paired intervals span zero. Refitting fixed designs on an independently acquired cohort shows predictive generalization need not imply generalization of input-use claims: dose contribution persists, whereas support for compound identity does not. CELLAUDIT adds a falsification layer to agentic model discovery, moving from generate-score-revise toward discover-falsify-revise.

Explore similar work

Apr 21, 2026cs.AI

AblateCell: A Reproduce-then-Ablate Agent for Virtual Cell Repositories

Systematic ablations are essential to attribute performance gains in AI Virtual Cells, yet they are rarely performed because biological repositories are under-standardized and tightly coupled to domain-specific data and formats. While recent coding agents can translate ideas into implementations, they typically stop at producing code and lack a verifier that can reproduce strong baselines and rigorously test which components truly matter. We introduce AblateCell, a reproduce-then-ablate agent for virtual cell repositories that closes this verification gap. AblateCell first reproduces reported baselines end-to-end by auto-configuring environments, resolving dependency and data issues, and rerunning official evaluations while emitting verifiable artifacts. It then conducts closed-loop ablation by generating a graph of isolated repository mutations and adaptively selecting experiments under a reward that trades off performance impact and execution cost. Evaluated on three single-cell perturbation prediction repositories (CPA, GEARS, BioLORD), AblateCell achieves 88.9% (+29.9% to human expert) end-to-end workflow success and 93.3% (+53.3% to heuristic) accuracy in recovering ground-truth critical components. These results enable scalable, repository-grounded verification and attribution directly on biological codebases.
Xue Xia, Chengkai Yao, Mingyu Tsoi +10
Aug 2, 2026cs.AI

Auditing Discovery Claims: A Two-Sided Criterion for Agentic Science, with the Negative Side Decidable

When a self-improving AI-for-science system claims a new capability, the evidence is usually a benchmark delta, a description-length gate, or a p-value. None separates a real gain from extra search, from a changed verifier, or from adaptation to a fallible oracle. We build a two-sided audit whose negative side is a formal fact: a pseudoknot-free oracle provably cannot represent a crossing base pair, so the prior verifier's range is bounded exactly, offline, before any run. "New" is relative to the agent's prior self, never to the base model. First, how far a single fallible oracle can inflate a capability claim. An invented, solver-free operator solves 43/60 crossing RNA targets under the predictor it optimizes, above a context-free floor of 0/60; under three predictors, 1/60 survives. Paired on the same 43 targets, a predictor the operator never saw confirms 2 of its designs against 26 for a minimum-free-energy solver (p = 8e-7). No statistic computed from the system and its own oracle sees that gap. Second, agent-written procedures can beat a human-written one under a judge no objective can flatter, at a fraction of the compute. Of six frontier models, the two whose operators ran without timeouts carry over at 0.293 against our 0.095 (n = 951 paired units, target-clustered [+0.108, +0.297], p = 5e-5) while spending 4.6-10x fewer oracle calls. Three rungs: difference under an outside adjudicator (reached), not bought with compute (reached, both directions), mechanism identified and transferable (not reached; seven candidates tested, none moves the statistic). The ceiling is the panel itself: its three predictors share nearest-neighbour thermodynamic parameters, two agreeing at kappa = 0.673. The audit is as unsparing about our own system: matched undirected search is an exact zero, and a search-free probe puts 84% of our headline effect on targets a random sequence already solves.
Wenhui Chen, Jianlin Chen, Ziyao Lin +1
Apr 22, 2026q-bio.QM

AROMA: Augmented Reasoning Over a Multimodal Architecture for Virtual Cell Genetic Perturbation Modeling

Virtual cell modeling predicts molecular state changes under genetic perturbations in silico, which is essential for biological mechanism studies. However, existing approaches suffer from unconstrained reasoning, uninterpretable predictions, and retrieval signals that are weakly aligned with regulatory topology. To address these limitations, we propose AROMA, an Augmented Reasoning Over a Multimodal Architecture for virtual cell genetic perturbation modeling. AROMA integrates textual evidence, graph-topology information, and protein sequence features to model perturbation-target dependencies, and is trained with a two-stage optimization strategy to yield predictions that are both accurate and interpretable. We also construct two knowledge graphs and a perturbation reasoning dataset, PerturbReason, containing more than 498k samples, as reusable resources for the virtual cell domain. Experiments show that AROMA outperforms existing methods across multiple cell lines, and remains robust under zero-shot evaluation on an unseen cell line, as well as in knowledge-sparse, long-tail scenarios. Overall, AROMA demonstrates that combining knowledge-driven multimodal modeling with evidence retrieval provides a promising pathway toward more reliable and interpretable virtual cell perturbation prediction. Model weights are available at https://huggingface.co/blazerye/AROMA. Code is available at https://github.com/blazerye/AROMA.
Zhenyu Wang, Geyan Ye, Wei Liu +1