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Guillaume Huguet

Doctorat - UdeM
Superviseur⋅e principal⋅e
Sujets de recherche
Apprentissage spectral
Biologie computationnelle
Modèles génératifs

Publications

High-effect gene-coding variants impact cognition, mental well-being, and neighborhood safety substrates in brain morphology
Kuldeep Kumar
Zohra Saci
Martineau Jean-Louis
Xiaoqian J. Chai
Tian Ge
B.T. Thomas Yeo
Paul M. Thompson
Carrie E. Bearden
Ole A. Andreassen
Sébastien Jacquemont
Our genetic makeup, together with environmental and social influences, shape our brain's development. Yet, the imaging genetics field has st… (voir plus)ruggled to integrate all these modalities to investigate the interplay between genetic blueprint, environment, human health, daily living skills and outcomes. Hence, we interrogated the Adolescent Brain Cognitive Development (ABCD) cohort to outline the effects of rare high-effect genetic variants on brain architecture and corresponding implications on cognitive, behavioral, psychosocial, and socioeconomic traits. Specifically, we designed a holistic pattern-learning algorithm that quantitatively dissects the impacts of copy number variations (CNVs) on brain structure and 962 behavioral variables spanning 20 categories in 7,657 adolescents. Our results reveal associations between genetic alterations, higher-order brain networks, and specific parameters of the family well-being (increased parental and child stress, anxiety and depression) or neighborhood dynamics (decreased safety); effects extending beyond the impairment of cognitive ability or language capacity, dominantly reported in the CNV literature. Our investigation thus spotlights a far-reaching interplay between genetic variation and subjective life quality in adolescents and their families.
High-effect gene-coding variants impact cognition, mental well-being, and neighborhood safety substrates in brain morphology
Kuldeep Kumar
Zohra Saci
Martineau Jean-Louis
Xiaoqian J. Chai
Tian Ge
B.T. Thomas Yeo
Paul M. Thompson
Carrie E. Bearden
Ole A. Andreassen
Sébastien Jacquemont
Our genetic makeup, together with environmental and social influences, shape our brain's development. Yet, the imaging genetics field has st… (voir plus)ruggled to integrate all these modalities to investigate the interplay between genetic blueprint, environment, human health, daily living skills and outcomes. Hence, we interrogated the Adolescent Brain Cognitive Development (ABCD) cohort to outline the effects of rare high-effect genetic variants on brain architecture and corresponding implications on cognitive, behavioral, psychosocial, and socioeconomic traits. Specifically, we designed a holistic pattern-learning algorithm that quantitatively dissects the impacts of copy number variations (CNVs) on brain structure and 962 behavioral variables spanning 20 categories in 7,657 adolescents. Our results reveal associations between genetic alterations, higher-order brain networks, and specific parameters of the family well-being (increased parental and child stress, anxiety and depression) or neighborhood dynamics (decreased safety); effects extending beyond the impairment of cognitive ability or language capacity, dominantly reported in the CNV literature. Our investigation thus spotlights a far-reaching interplay between genetic variation and subjective life quality in adolescents and their families.
295. Rare Variant Genetic Architecture of the Human Cortical MRI Phenotypes in General Population
Kuldeep Kumar
Sayeh Kazem
Zhijie Liao
Thomas Renne
Martineau Jean‐Louis
Zhe Xie
Zohra Saci
Laura Almasy
David C. Glahn
Tomáš Paus
Carrie E. Bearden
Paul M. Thompson
Richard A. I. Bethlehem
Varun Warrier
Sébastien Jacquemont
Improving and Generalizing Flow-Based Generative Models with Minibatch Optimal Transport
Continuous normalizing flows (CNFs) are an attractive generative modeling technique, but they have been held back by limitations in their si… (voir plus)mulation-based maximum likelihood training. We introduce the generalized \textit{conditional flow matching} (CFM) technique, a family of simulation-free training objectives for CNFs. CFM features a stable regression objective like that used to train the stochastic flow in diffusion models but enjoys the efficient inference of deterministic flow models. In contrast to both diffusion models and prior CNF training algorithms, CFM does not require the source distribution to be Gaussian or require evaluation of its density. A variant of our objective is optimal transport CFM (OT-CFM), which creates simpler flows that are more stable to train and lead to faster inference, as evaluated in our experiments. Furthermore, OT-CFM is the first method to compute dynamic OT in a simulation-free way. Training CNFs with CFM improves results on a variety of conditional and unconditional generation tasks, such as inferring single cell dynamics, unsupervised image translation, and Schrödinger bridge inference.
Assessing Neural Network Representations During Training Using Noise-Resilient Diffusion Spectral Entropy
Danqi Liao
Chen Liu
Benjamin W Christensen
Maximilian Nickel
Ian Adelstein
Entropy and mutual information in neural networks provide rich information on the learning process, but they have proven difficult to comput… (voir plus)e reliably in high dimensions. Indeed, in noisy and high-dimensional data, traditional estimates in ambient dimensions approach a fixed entropy and are prohibitively hard to compute. To address these issues, we leverage data geometry to access the underlying manifold and reliably compute these information-theoretic measures. Specifically, we define diffusion spectral entropy (DSE) in neural representations of a dataset as well as diffusion spectral mutual information (DSMI) between different variables representing data. First, we show that they form noise-resistant measures of intrinsic dimensionality and relationship strength in high-dimensional simulated data that outperform classic Shannon entropy, nonparametric estimation, and mutual information neural estimation (MINE). We then study the evolution of representations in classification networks with supervised learning, self-supervision, or overfitting. We observe that (1) DSE of neural representations increases during training; (2) DSMI with the class label increases during generalizable learning but stays stagnant during overfitting; (3) DSMI with the input signal shows differing trends: on MNIST it increases, while on CIFAR-10 and STL-10 it decreases. Finally, we show that DSE can be used to guide better network initialization and that DSMI can be used to predict downstream classification accuracy across 962 models on ImageNet.
Sequence-Augmented SE(3)-Flow Matching For Conditional Protein Backbone Generation
Simulation-Free Schrödinger Bridges via Score and Flow Matching
We present simulation-free score and flow matching ([SF]…
F66. FROM GENE TO COGNITION: MAPPING THE EFFECTS OF GENOMIC DELETIONS AND DUPLICATIONS ON COGNITIVE ABILITY
Sayeh Kazem
Kuldeep Kumar
Thomas Renne
Martineau Jean-Louis
Zohra Saci
Laura Almasy
David Glahn
Sébastien Jacquemont
W56. UNRAVELING THE IMPACT OF GENOMIC VARIATIONS ON COGNITIVE ABILITY ACROSS THE HUMAN CORTEX: INSIGHTS FROM GENE EXPRESSION AND COPY NUMBER VARIANTS
Kuldeep Kumar
Sayeh Kazem
Thomas Renne
Bank Engchuan
Omar Shanta
Bhooma Thiruvahindrapuram
J. MacDonald
Marieke Klein
Stephen W Scherer
Laura Almasy
Jonathan Sebat
David C. Glahn
Sébastien Jacquemont
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
Kuldeep Kumar
Claudia Modenato
Clara A. Moreau
C. Ching
Christopher R. K. Ching
Annabelle Harvey
Sandra Martin-Brevet
Martineau Jean-Louis
Elise Douard
Charles-Olivier Martin
C.O. Martin
Nadine Younis
Petra Tamer
Anne M. Maillard
Borja Rodriguez-Herreros
Aurélie Pain
Sonia Richetin
Leila Kushan
Dmitry Isaev … (voir 26 de plus)
Kathryn Alpert
Anjani Ragothaman
Jessica A. Turner
Wei Wang
T. Ho
Tiffany C. Ho
Lianne Schmaal
Ana I. Silva
Marianne B.M. van den Bree
V. Marianne
David E.J. Linden
M. J. Owen
Marie Owen
Jeremy Hall
Sarah Lippé
Bogdan Draganski
Boris A. Gutman
Ida E. Sønderby
Ole A. Andreassen
Laura Schultz
Laura Almasy
David C. Glahn
Carrie E. Bearden
Paul M. Thompson
Sébastien Jacquemont
OBJECTIVE Copy number variants (CNVs) are well-known genetic pleiotropic risk factors for multiple neurodevelopmental and psychiatric disord… (voir plus)ers (NPDs), including autism (ASD) and schizophrenia. Little is known about how different CNVs conferring risk for the same condition may affect subcortical brain structures and how these alterations relate to the level of disease risk conferred by CNVs. To fill this gap, the authors investigated gross volume, vertex-level thickness, and surface maps of subcortical structures in 11 CNVs and six NPDs. METHODS Subcortical structures were characterized using harmonized ENIGMA protocols in 675 CNV carriers (CNVs at 1q21.1, TAR, 13q12.12, 15q11.2, 16p11.2, 16p13.11, and 22q11.2; age range, 6-80 years; 340 males) and 782 control subjects (age range, 6-80 years; 387 males) as well as ENIGMA summary statistics for ASD, schizophrenia, attention deficit hyperactivity disorder, obsessive-compulsive disorder, bipolar disorder, and major depression. RESULTS All CNVs showed alterations in at least one subcortical measure. Each structure was affected by at least two CNVs, and the hippocampus and amygdala were affected by five. Shape analyses detected subregional alterations that were averaged out in volume analyses. A common latent dimension was identified, characterized by opposing effects on the hippocampus/amygdala and putamen/pallidum, across CNVs and across NPDs. Effect sizes of CNVs on subcortical volume, thickness, and local surface area were correlated with their previously reported effect sizes on cognition and risk for ASD and schizophrenia. CONCLUSIONS The findings demonstrate that subcortical alterations associated with CNVs show varying levels of similarities with those associated with neuropsychiatric conditions, as well distinct effects, with some CNVs clustering with adult-onset conditions and others with ASD. These findings provide insight into the long-standing questions of why CNVs at different genomic loci increase the risk for the same NPD and why a single CNV increases the risk for a diverse set of NPDs.
Neural FIM for learning Fisher information metrics from point cloud data
Oluwadamilola Fasina
Yanlei Zhang
Maximilian Nickel
Ian Adelstein
Although data diffusion embeddings are ubiquitous in unsupervised learning and have proven to be a viable technique for uncovering the under… (voir plus)lying intrinsic geometry of data, diffusion embeddings are inherently limited due to their discrete nature. To this end, we propose neural FIM, a method for computing the Fisher information metric (FIM) from point cloud data - allowing for a continuous manifold model for the data. Neural FIM creates an extensible metric space from discrete point cloud data such that information from the metric can inform us of manifold characteristics such as volume and geodesics. We demonstrate Neural FIM's utility in selecting parameters for the PHATE visualization method as well as its ability to obtain information pertaining to local volume illuminating branching points and cluster centers embeddings of a toy dataset and two single-cell datasets of IPSC reprogramming and PBMCs (immune cells).
Graph Fourier MMD for Signals on Graphs
While numerous methods have been proposed for computing distances between probability distributions in Euclidean space, relatively little at… (voir plus)tention has been given to computing such distances for distributions on graphs. However, there has been a marked increase in data that either lies on graph (such as protein interaction networks) or can be modeled as a graph (single cell data), particularly in the biomedical sciences. Thus, it becomes important to find ways to compare signals defined on such graphs. Here, we propose Graph Fourier MMD (GFMMD), a novel distance between distributions and signals on graphs. GFMMD is defined via an optimal witness function that is both smooth on the graph and maximizes difference in expectation between the pair of distributions on the graph. We find an analytical solution to this optimization problem as well as an embedding of distributions that results from this method. We also prove several properties of this method including scale invariance and applicability to disconnected graphs. We showcase it on graph benchmark datasets as well on single cell RNA-sequencing data analysis. In the latter, we use the GFMMD-based gene embeddings to find meaningful gene clusters. We also propose a novel type of score for gene selection called "gene localization score" which helps select genes for cellular state space characterization.