Portrait of Flavie Lavoie-Cardinal

Flavie Lavoie-Cardinal

Associate Academic Member
Associate Professor, Université Laval, Department of Psychiatry and Neurosciences
Research Topics
AI for Science
AI in Health
Anomaly Detection
Applied AI
Biophysics
Computational Biology
Computational Neuroscience
Computer Vision
Deep Learning
Foundation Models
Generative Models
Medical Image Segmentation
NeuroAI
Neuroscience

Biography

Dr. Lavoie-Cardinal is an is an Associate Professor to the Department of Psychiatry and Neuroscience at Université Laval, Québec, Canada, and a NSERC Tier 2 Canadian Research Chair in Intelligent Nanoscopy of Cellular Plasticity. She is also a principal investigator at the CERVO Brain Research Center and the Health and Life Science research axis leader at the Institute for Intelligence and Data in Québec city.

She is the Perception and Control axis co-leader in the Neuro-AI strategic regroupment UNIQUE and one of the co-leader of the Neuro-AI regroupment 1 at IVADO. She obtained her PhD in Chemistry in 2011, followed by two postdoctoral fellowships, one of which was in the group of Prof. Dr. Dr. Stefan Hell (2014 Chemistry Nobel Prize) on the development of super-resolution microscopy techniques.

She now leads a research group of 14 graduate and undergraduate students working the interface of optical microscopy, neuroscience and artificial intelligence (AI). Her transdisciplinary research program aims at developing novel AI-assisted bioimaging strategies to uncover the molecular signature of altered synaptic plasticity, leading to neurodegeration or cognitive impairment.

Publications

Enhancing STED Microscopy via Fluorescence Lifetime Unmixing and Filtering in Two-Species SPLIT-STED
Andréanne Deschênes
Antoine Ollier
Marie Lafontaine
Albert Michaud-Gagnon
Jeffrey-Gabriel Steavan Santiague
Anthony Bilodeau
Paul De Koninck
A Self-Supervised Foundation Model for Robust and Generalizable Representation Learning in STED Microscopy
Anthony Bilodeau
Julia Chabbert
Kamylle Thériault
Andréanne Deschênes
Jean-Michel Bellavance
Koraly Lessard
Renaud Bernatchez
Paul De Koninck
Foundation Models (FMs) have dramatically increased the potential and power of deep learning algorithms through general capacities over a va… (see more)riety of tasks. The performance increase they offer is obtained without elaborated specific trainings for domains such as natural language processing and computer vision. However, their application in specialized fields like biomedical imaging and fluorescence microscopy remains difficult due to distribution shifts and the scarcity of high-quality annotated datasets. The high cost of data acquisition and the requirement for in-domain expertise further exacerbate this challenge in microscopy. To address this we introduce STED-FM, a foundation model specifically designed for super-resolution STimulated Emission Depletion (STED) microscopy. STED-FM leverages a Vision Transformer architecture trained at scale with Masked Autoencoding on a new dataset of nearly one million STED images. STED-FM learns expressive latent representations without requiring extensive annotations, yielding robust performance across diverse downstream microscopy image analysis tasks. Unsupervised experiments demonstrate the discriminative structure of its learned latent space. These representations can be leveraged for multiple downstream applications, including fully supervised classification and segmentation with reduced annotation requirements. Moreover, STED-FM representations enhance the performance of deep learning–based image denoising and improve the quality of images generated by diffusion models, enabling latent attribute manipulation for the data-driven discovery of subtle nanostructures and phenotypes, as well as algorithmic super-resolution. Moreover, its powerful structure retrieval capabilities are integrated into automated STED microscopy acquisition pipelines, paving the way for smart microscopy. In sum, we demonstrate that STED-FM lays a robust foundation for state-of-the-art algorithms across a wide array of tasks, establishing it as a highly valuable and scalable resource for researchers in super-resolution microscopy.
Quantitative Analysis of Miniature Synaptic Calcium Transients Using Positive Unlabeled Deep Learning
Anthony Bilodeau
Theresa Wiesner
Gabriel Leclerc
Mado Lemieux
Gabriel Nadeau
Katrine Castonguay
Bolin Fan
Simon Labrecque
Renée Hložek
Paul De Koninck
Ca 2+ imaging methods are widely used for studying cellular activity in the brain, allowing detailed ana… (see more)lysis of dynamic processes across various scales. Enhanced by high-contrast optical microscopy and fluorescent Ca 2+ sensors, this technique can be used to reveal localized Ca 2+ fluctuations within neurons, including in sub-cellular compartments, such as the dendritic shaft or spines. Despite advances in Ca 2+ sensors, the analysis of miniature Synaptic Calcium Transients (mSCTs), characterized by variability in morphology and low signal-to-noise ratios, remains challenging. Traditional threshold-based methods struggle with the detection and segmentation of these small, dynamic events. Deep learning (DL) approaches offer promising solutions but are limited by the need for large annotated datasets. Positive Unlabeled (PU) learning addresses this limitation by leveraging unlabeled instances to increase dataset size and enhance performance. This approach is particularly useful in the case of mSCTs that are scarce and small, associated with a very small proportion of the foreground pixels. PU learning significantly increases the effective size of the training dataset, improving model performance. Here, we present a PU learning-based strategy for detecting and segmenting mSCTs. We evaluate the performance of two 3D deep learning models, StarDist-3D and 3D U-Net, which are well established for the segmentation of small volumetric structures in microscopy datasets. By integrating PU learning, we enhance the 3D U-Net’s performance, demonstrating significant gains over traditional methods. This work pioneers the application of PU learning in Ca 2+ imaging analysis, offering a robust framework for mSCT detection and segmentation. We also demonstrate how this quantitative analysis pipeline can be used for subsequent mSCTs feature analysis. We characterize morphological and kinetic changes of mSCTs associated with the application of chemical long-term potentiation (cLTP) stimulation in cultured rat hippocampal neurons. Our data-driven approach shows that a cLTP-inducing stimulus leads to the emergence of new active dendritic regions and differently affects mSCTs subtypes.
Development of AI-assisted microscopy frameworks through realistic simulation with pySTED
Anthony Bilodeau
Albert Michaud-Gagnon
Julia Chabbert
Benoit Turcotte
Jörn Heine
The integration of artificial intelligence into microscopy systems significantly enhances performance, optimizing both image acquisition and… (see more) analysis phases. Development of artificial intelligence-assisted super-resolution microscopy is often limited by access to large biological datasets, as well as by difficulties to benchmark and compare approaches on heterogeneous samples. We demonstrate the benefits of a realistic stimulated emission depletion microscopy simulation platform, pySTED, for the development and deployment of artificial intelligence strategies for super-resolution microscopy. pySTED integrates theoretically and empirically validated models for photobleaching and point spread function generation in stimulated emission depletion microscopy, as well as simulating realistic point-scanning dynamics and using a deep learning model to replicate the underlying structures of real images. This simulation environment can be used for data augmentation to train deep neural networks, for the development of online optimization strategies and to train reinforcement learning models. Using pySTED as a training environment allows the reinforcement learning models to bridge the gap between simulation and reality, as showcased by its successful deployment on a real microscope system without fine tuning.
Filtering Pixel Latent Variables for Unmixing Noisy and Undersampled Volumetric Images
Andréanne Deschênes
Vincent Boulanger
Jean-Michel Bellavance
Julia Chabbert
Alexy Pelletier-Rioux
Resolution enhancement with a task-assisted GAN to guide optical nanoscopy image analysis and acquisition
Theresa Wiesner
Andréanne Deschênes
Anthony Bilodeau
Benoit Turcotte
Filtering Pixel Latent Variables for Unmixing Volumetric Images
Measurements of different overlapping components require robust unmixing algorithms to convert the raw multi-dimensional measurements to use… (see more)ful unmixed images. Such algorithms perform reliable separation of the components when the raw signal is fully resolved and contains enough information to fit curves on the raw distributions. In experimental physics, measurements are often noisy, undersam-pled, or unresolved spatially or spectrally. We propose a novel method where bandpass filters are applied to the latent space of a multi-dimensional convolutional neural network to separate the overlapping signal components and extract each of their relative contributions. Simultaneously processing all dimensions with multi-dimensional convolution kernels empowers the network to combine the information from adjacent pixels and time-or spectral-bins, facilitating component separation in instances where individual pixels lack well-resolved information. We demonstrate the applicability of the method to real experimental physics problems using fluorescence lifetime microscopy and mode decomposition in optical fibers as test cases. The successful application of our approach to these two distinct experimental cases, characterized by different measured distributions, highlights the versatility of our approach in addressing a wide array of imaging tasks.
Annotation Cost-Sensitive Deep Active Learning with Limited Data (Student Abstract)
Contextual bandit optimization of super-resolution microscopy
Anthony Bilodeau
Renaud Bernatchez
Albert Michaud-Gagnon
Microscopy analysis neural network to solve detection, enumeration and segmentation from image-level annotations
Anthony Bilodeau
Constantin V.L. Delmas
Martin Parent
Paul De Koninck
Neuronal activity remodels the F-actin based submembrane lattice in dendrites but not axons of hippocampal neurons
Anthony Bilodeau
Mado Lemieux
Marc-André Gardner
Theresa Wiesner
Gabrielle Laramée
Paul De Koninck