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Reed Naidoo

Publications and source records attributed to Reed Naidoo.

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Probing, Fusion, and Trustworthiness: A Systematic Evaluation of Foundation Model Representations for Multimodal Cancer Analysis

Foundation models (FMs) have emerged as powerful representation extractors for medical data, yet their generalizability to datasets under distribution shift remains underexplored. This work systematically evaluates FM-based representations on a suite of computational pathology tasks across two real-world commercial cohorts, IH-BC and IH-NSCLC, drawn from the licensed in-house (IH) oncology dataset. The analysis focuses on two modalities, whole-slide images and transcriptomic profiles, drawn from the IH multimodal data. We first benchmark unimodal probing performance across five FMs on eight downstream classification tasks, and find that image and omics representations carry complementary predictive signals. Then we investigate whether multimodal fusion can yield additional gains over unimodal baselines by comparing three image-omics fusion strategies built on paired representations. The trustworthiness of selected unimodal and multimodal pipelines is further assessed through conformal prediction. Our results show that FM representations achieve competitive performance on out-of-distribution data and that multimodal fusion helps mainly when no single modality dominates the signal. Conformal prediction reveals that in the majority of cases where a point prediction fails, the true diagnosis remains recoverable within the prediction set, reinforcing the value of uncertainty-aware inference for clinical support.

cs.LG

Morphologically Intelligent Perturbation Prediction with FORM

Understanding how cells respond to external stimuli is a central challenge in biomedical research and drug development. Current computational frameworks for modelling cellular responses remain restricted to two-dimensional representations, limiting their capacity to capture the complexity of cell morphology under perturbation. This dimensional constraint poses a critical bottleneck for the development of accurate virtual cell models. Here, we present FORM, a machine learning framework for predicting perturbation-induced changes in three-dimensional cellular structure. FORM consists of two components: a morphology encoder, trained end-to-end via a novel multi-channel VQGAN to learn compact 3D representations of cell shape, and a diffusion-based perturbation trajectory module that captures how morphology evolves across perturbation conditions. Trained on a large-scale dataset of over 65,000 multi-fluorescence 3D cell volumes spanning diverse chemical and genetic perturbations, FORM supports both unconditional morphology synthesis and conditional simulation of perturbed cell states. Beyond generation, FORM can predict downstream signalling activity, simulate combinatorial perturbation effects, and model morphodynamic transitions between states of unseen perturbations. To evaluate performance, we introduce MorphoEval, a benchmarking suite that quantifies perturbation-induced morphological changes in structural, statistical, and biological dimensions. Together, FORM and MorphoEval work toward the realisation of the 3D virtual cell by linking morphology, perturbation, and function through high-resolution predictive simulation.

cs.CV