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Barbara Bodinier

Publications and source records attributed to Barbara Bodinier.

4 recordsLinked to original sources

Can AI Scientist Agents Learn from Lab-in-the-Loop Feedback? Evidence from Iterative Perturbation Discovery

Recent work has questioned whether large language models (LLMs) can perform genuine in-context learning (ICL) for scientific experimental design, with prior studies suggesting that LLM-based agents exhibit no sensitivity to experimental feedback. We shed new light on this question by carrying out 800 independently replicated experiments on iterative perturbation discovery in Cell Painting high-content screening. We compare an LLM agent that iteratively updates its hypotheses using experimental feedback to a zero-shot baseline that relies solely on pretraining knowledge retrieval. Access to feedback yields a $+53.4\%$ increase in discoveries per feature on average ($p = 0.003$). To test whether this improvement arises from genuine feedback-driven learning rather than prompt-induced recall of pretraining knowledge, we introduce a random feedback control in which hit/miss labels are permuted. Under this control, the performance gain disappears, indicating that the observed improvement depends on the structure of the feedback signal ($+13.0$ hits, $p = 0.003$). We further examine how model capability affects feedback utilization. Upgrading from Claude Sonnet 4.5 to 4.6 reduces gene hallucination rates from ${\sim}33\%$--$45\%$ to ${\sim}3$--$9\%$, converting a non-significant ICL effect ($+0.8$, $p = 0.32$) into a large and highly significant improvement ($+11.0$, $p=0.003$) for the best ICL strategy. These results suggest that effective in-context learning from experimental feedback emerges only once models reach a sufficient capability threshold.

cs.LG

Predicting gene essentiality and drug response from perturbation screens in preclinical cancer models with LEAP: Layered Ensemble of Autoencoders and Predictors

High-throughput preclinical perturbation screens, where the effects of genetic, chemical, or environmental perturbations are systematically tested on disease models, hold significant promise for machine learning-enhanced drug discovery due to their scale and causal nature. Predictive models trained on such datasets can be used to (i) infer perturbation response for previously untested disease models, and (ii) characterise the biological context that affects perturbation response. Existing predictive models suffer from limited reproducibility, generalisability and interpretability. To address these issues, we introduce a framework of Layered Ensemble of Autoencoders and Predictors (LEAP), a general and flexible ensemble strategy to aggregate predictions from multiple regressors trained using diverse gene expression representation models. LEAP consistently improves prediction performances in unscreened cell lines across modelling strategies. In particular, LEAP applied to perturbation-specific LASSO regressors (PS-LASSO) provides a favorable balance between near state-of-the-art performance and low computation time. We also propose an interpretability approach combining model distillation and stability selection to identify important biological pathways for perturbation response prediction in LEAP. Our models have the potential to accelerate the drug discovery pipeline by guiding the prioritisation of preclinical experiments and providing insights into the biological mechanisms involved in perturbation response. The code and datasets used in this work are publicly available.

cs.LG

Automated calibration of consensus weighted distance-based clustering approaches using sharp

In consensus clustering, a clustering algorithm is used in combination with a subsampling procedure to detect stable clusters. Previous studies on both simulated and real data suggest that consensus clustering outperforms native algorithms. We extend here consensus clustering to allow for attribute weighting in the calculation of pairwise distances using existing regularised approaches. We propose a procedure for the calibration of the number of clusters (and regularisation parameter) by maximising a novel consensus score calculated directly from consensus clustering outputs, making it extremely computationally competitive. Our simulation study shows better clustering performances of (i) models calibrated by maximising our consensus score compared to existing calibration scores, and (ii) weighted compared to unweighted approaches in the presence of features that do not contribute to cluster definition. Application on real gene expression data measured in lung tissue reveals clear clusters corresponding to different lung cancer subtypes. The R package sharp (version 1.4.0) is available on CRAN.

stat.ME

Automated calibration for stability selection in penalised regression and graphical models

Stability selection represents an attractive approach to identify sparse sets of features jointly associated with an outcome in high-dimensional contexts. We introduce an automated calibration procedure via maximisation of an in-house stability score and accommodating a priori-known block structure (e.g. multi-OMIC) data. It applies to (LASSO) penalised regression and graphical models. Simulations show our approach outperforms non-stability-based and stability selection approaches using the original calibration. Application of multi-block graphical LASSO on real (epigenetic and transcriptomic) data from the Norwegian Women and Cancer study reveals a central/credible and novel cross-OMIC role of LRRN3 in the biological response to smoking. Proposed approaches were implemented in the R package sharp.

stat.ME