Ce programme soutient les startups spécialisées en IA à tout moment de l'année. Bénéficiez de ressources de pointe et d'un accompagnement sur mesure pour accélérer le développement de votre technologie.
Offert par Mila et le Forum des politiques publiques, ce programme est conçu pour outiller les décideur·euse·s et les responsables des politiques publiques à naviguer efficacement à travers les opportunités et les risques liés à l'IA. La prochaine cohorte se tiendra en français les 1er et 2 septembre 2026 à Mila.
Échangez avec les conseiller·ère·s académiques de Mila ainsi que des étudiant·e·s-chercheur·euse·s pour en savoir plus sur la communauté de Mila et découvrir comment nous rejoindre les 19 et 31 août et le 11 septembre 2026.
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Lecteur Multimédia
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Publications
Predictive Performance Precision Analysis in Medicine: Identification of low-confidence predictions at patient and profile levels (MED3pa I)
Artificial Intelligence models are increasingly used in healthcare, yet global performance metrics can mask variations in reliability across… (voir plus) individual patients or subgroups with shared attributes, called
patient profiles
. This study introduces MED3pa, a method that identifies when models are less reliable, allowing clinicians to better assess model limitations.
We propose a framework that estimates predictive confidence using three combined approaches: Individualized (IPC), Aggregated (APC), and Mixed Predictive Confidence (MPC). IPC estimates confidence for each patient, APC assesses it across profiles, and MPC combines both. We evaluate our method on four datasets: one simulated, two public, and one private clinical dataset. Metrics by Declaration Rate (MDR) curves show how performance changes when retaining only the most confident predictions, while interpretable decision trees reveal profiles with higher or lower model confidence.
We demonstrate our method in internal, temporal, and external validation settings, as well as through a clinical example. In internal validation, limiting predictions to the 93% most confident cases improved sensitivity by 14.3% and the AUC by 5.1%. In the clinical example, MED3pa identified a patient profile with high misclassification risk, demonstrating its potential for safer deployment.
By identifying low-confidence predictions, our framework improves model reliability in clinical settings. It can be integrated into decision support systems to help clinicians make more informed decisions. Confidence thresholds help balance model performance with the proportion of patients for whom predictions are considered reliable.
Better leveraging confidence in model predictions could improve reliability and trustworthiness, supporting safer and more effective use in healthcare.
While neural networks are capable of achieving human-like performance in many tasks such as image classification, the impressive performance… (voir plus) of each model is limited to its own dataset. Source-free domain adaptation (SFDA) was introduced to address knowledge transfer between different domains in the absence of source data, thus, increasing data privacy. Diversity in representation space can be vital to a model`s adaptability in varied and difficult domains. In unsupervised SFDA, the diversity is limited to learning a single hypothesis on the source or learning multiple hypotheses with a shared feature extractor. Motivated by the improved predictive performance of ensembles, we propose a novel unsupervised SFDA algorithm that promotes representational diversity through the use of separate feature extractors with Distinct Backbone Architectures (DBA). Although diversity in feature space is increased, the unconstrained mutual information (MI) maximization may potentially introduce amplification of weak hypotheses. Thus we introduce the Weak Hypothesis Penalization (WHP) regularizer as a mitigation strategy. Our work proposes Penalized Diversity (PD) where the synergy of DBA and WHP is applied to unsupervised source-free domain adaptation for covariate shift. In addition, PD is augmented with a weighted MI maximization objective for label distribution shift. Empirical results on natural, synthetic, and medical domains demonstrate the effectiveness of PD under different distributional shifts.
Uncovering executive function profiles within interindividual variability: A data driven clustering exploration of design fluency in school-aged children
Large collections of high-dimensional data have become nearly ubiquitous across many academic fields and application domains, ranging from b… (voir plus)iology to the humanities. Since working directly with high-dimensional data poses challenges, the demand for algorithms that create low-dimensional representations, or embeddings, for data visualization, exploration, and analysis is now greater than ever. In recent years, numerous embedding algorithms have been developed, and their usage has become widespread in research and industry. This surge of interest has resulted in a large and fragmented research field that faces technical challenges alongside fundamental debates, and it has left practitioners without clear guidance on how to effectively employ existing methods. Aiming to increase coherence and facilitate future work, in this review we provide a detailed and critical overview of recent developments, derive a list of best practices for creating and using low-dimensional embeddings, evaluate popular approaches on a variety of datasets, and discuss the remaining challenges and open problems in the field.
We investigate the robustness of Neural Ratio Estimators (NREs) and Neural Posterior Estimators (NPEs) to distributional shifts in the conte… (voir plus)xt of measuring the abundance of dark matter subhalos using strong gravitational lensing data. While these data-driven inference frameworks can be accurate on test data from the same distribution as the training sets, in real applications, it is expected that simulated training data and true observational data will differ in their distributions. We explore the behavior of a trained NRE and trained sequential NPEs to estimate the population-level parameters of dark matter subhalos from a large sample of images of strongly lensed galaxies with test data presenting distributional shifts within and beyond the bounds of the training distribution in the nuisance parameters (e.g., the background source morphology). While our results show that NREs and NPEs perform well when tested perfectly in distribution, they exhibit significant biases when confronted with slight deviations from the examples seen in the training distribution. This indicates the necessity for caution when applying NREs and NPEs to real astrophysical data, where high-dimensional underlying distributions are not perfectly known.
RadiSeq: a single- and bulk-cell whole-genome DNA sequencing simulator for radiation-damaged cell models
Felix Mathew
Luc Galarneau
J. Kildea
Objective To build and validate a simulation framework to perform single-cell and bulk-cell whole genome sequencing simulation of radiation-… (voir plus)exposed Monte Carlo cell models to assist radiation genomics studies. Approach Sequencing the genomes of radiation-damaged cells can provide useful insight into radiation action for radiobiology research. However, carrying out post-irradiation sequencing experiments can often be challenging, expensive, and time-consuming. Although computational simulations have the potential to provide solutions to these experimental challenges, and aid in designing optimal experiments, the absence of tools currently limits such application. Monte Carlo toolkits exist to simulate radiation exposures of cell models but there are no tools to simulate single- and bulk-cell sequencing of cell models containing radiation-damaged DNA. Therefore, we aimed to develop a Monte Carlo simulation framework to address this gap by designing a tool capable of simulating sequencing processes for radiation-damaged cells. Main Results We developed RadiSeq – a multi-threaded whole-genome DNA sequencing simulator written in C++. RadiSeq can be used to simulate Illumina sequencing of radiation-damaged cell models produced by Monte Carlo simulations. RadiSeq has been validated through comparative analysis, where simulated data were matched against experimentally obtained data, demonstrating reasonable agreement between the two. Additionally, it comes with numerous features designed to closely resemble actual whole-genome sequencing. RadiSeq is also highly customizable with a single input parameter file. Significance RadiSeq enables the research community to perform complex simulations of radiation-exposed DNA sequencing, supporting the optimization, planning, and validation of costly and time-intensive radiation biology experiments. This framework provides a powerful tool for advancing radiation genomics research.