A postdoc position is available under the shared supervision of Prof. Maxime Baud and Dr. Timothée Proix, who both specialize in quantitative neuroscience research. Together, they are running a three-year clinical trial involving patients with epilepsy who received a minimally invasive EEG device beneath the scalp for the chronic recording (months) of brain signals during wake and sleep. The postdoc will help with the analysis of massive amounts of EEG data, with a desire to build forecasting algorithms aiming at estimating the risk of seizures 24 hours in advance. The project lies at the interface between machine learning and EEG data analysis. The goal of the project is to develop machine learning algorithms to forecast seizures.

We have an opening for a postdoc position investigating the neural bases of deep multimodal learning in the brain. The project involves EEG and laminar 7T imaging (in collaboration with Dr. Peter Bandettini’s lab at NIMH) to test computational hypotheses for how the brain learns multimodal concept representations. Responsibilities of the postdoc include running EEG and fMRI experiments, data analysis and manuscript preparation. Georgetown University has a vibrant neuroscience community with over fifty labs participating in the Interdisciplinary Program in Neuroscience and a number of relevant research centers, including the new Center for Neuroengineering (cne.georgetown.edu). Interested candidates should submit a CV, a brief (1 page) statement of research interests, representative reprints, and the names and contact information of three references to Interfolio via https://apply.interfolio.com/148520. Faxed, emailed, or mailed applications will not be accepted. Questions about the position can be directed to Maximilian Riesenhuber (mr287@georgetown.edu).

The Grossman Center for Quantitative Biology and Human Behavior at the University of Chicago seeks outstanding applicants for multiple postdoctoral positions in computational and theoretical neuroscience. We especially welcome applicants who develop mathematical approaches, computational models, and machine learning methods to study the brain at the circuits, systems, or cognitive levels. The current faculty members of the Grossman Center to work with are: Brent Doiron’s lab investigates how the cellular and synaptic circuitry of neuronal circuits supports the complex dynamics and computations that are routinely observed in the brain. Jorge Jaramillo’s lab investigates how subcortical structures interact with cortical circuits to subserve cognitive processes such as memory, attention, and decision making. Ramon Nogueira’s lab investigates the geometry of representations as the computational support of cognitive processes like abstraction in noisy artificial and biological neural networks. Marcella Noorman’s lab investigates how properties of synapses, neurons, and circuits shape the neural dynamics that enable flexible and efficient computation. Samuel Muscinelli’s lab studies how the anatomy of brain circuits both governs learning and adapts to it. We combine analytical theory, machine learning, and data analysis, in close collaboration with experimentalists. Appointees will have access to state-of-the-art facilities and multiple opportunities for collaboration with exceptional experimental labs within the Neuroscience Institute, as well as other labs from the departments of Physics, Computer Sciences, and Statistics. The Grossman Center offers competitive postdoctoral salaries in the vibrant and international city of Chicago, and a rich intellectual environment that includes the Argonne National Laboratory and UChicago’s Data Science Institute. The Neuroscience Institute is currently engaged in a major expansion that includes the incorporation of several new faculty members in the next few years.

We are pleased to announce the opening of a PhD position at INMED (Aix-Marseille University) through the SCHADOC program, focused on the neural coding of social interactions and memory in the cortex of behaving mice. The project will investigate how social behaviors essential for cooperation, mating, and group dynamics are encoded in the brain, and how these processes are disrupted in neurodevelopmental disorders such as autism. This project uses longitudinal calcium imaging and population-level data analysis to study how cortical circuits encode social interactions in mice. Recordings from mPFC and S1 in wild-type and Neurod2 KO mice will be used to extract neural representations of social memory. The candidate will develop and apply computational models of neural dynamics and representational geometry to uncover how these codes evolve over time and are disrupted in social amnesia.

Understanding how brains learn requires bridging evidence across scales—from behaviour and neural circuits to cells, synapses, and molecules. In our work, we use computational modelling and data analysis to explore how the physical properties of neurons and neural circuits constrain learning. These include limits imposed by brain wiring, energy availability, molecular noise, and the 3D structure of dendritic spines. In this talk I will describe one such project testing if wiring motifs from fly brain connectomes can improve performance of reservoir computers, a type of recurrent neural network. The hope is that these insights into brain learning will lead to improved learning algorithms for artificial systems.

This webinar features presentations from SueYeon Chung (New York University) and Srinivas Turaga (HHMI Janelia Research Campus) on theoretical and computational approaches to sensory cognition. Chung introduced a “neural manifold” framework to capture how high-dimensional neural activity is structured into meaningful manifolds reflecting object representations. She demonstrated that manifold geometry—shaped by radius, dimensionality, and correlations—directly governs a population’s capacity for classifying or separating stimuli under nuisance variations. Applying these ideas as a data analysis tool, she showed how measuring object-manifold geometry can explain transformations along the ventral visual stream and suggested that manifold principles also yield better self-supervised neural network models resembling mammalian visual cortex. Turaga described simulating the entire fruit fly visual pathway using its connectome, modeling 64 key cell types in the optic lobe. His team’s systematic approach—combining sparse connectivity from electron microscopy with simple dynamical parameters—recapitulated known motion-selective responses and produced novel testable predictions. Together, these studies underscore the power of combining connectomic detail, task objectives, and geometric theories to unravel neural computations bridging from stimuli to cognitive functions.

It is now widely accepted that openness and transparency are keys to improving the reproducibility of scientific research, but many challenges remain to adoption of these practices. I will discuss the growth of an ecosystem for open science within the field of neuroimaging, focusing on platforms for open data sharing and open source tools for reproducible data analysis. I will also discuss the role of the Brain Imaging Data Structure (BIDS), a community standard for data organization, in enabling this open science ecosystem, and will outline the scientific impacts of these resources.

This course provides a fundamental foundation in the modern techniques of experimental neuroscience. It introduces the essentials of sensors, motor control, microcontrollers, programming, data analysis, and machine learning by guiding students through the “hands on” construction of an increasingly capable robot. In parallel, related concepts in neuroscience are introduced as nature’s solution to the challenges students encounter while designing and building their own intelligent system.

In systems neuroscience, datasets are multimodal and include data-streams of various origins: multichannel electrophysiology, 1- or 2-p calcium imaging, behavior, etc. Often, the exact nature of data streams are unique to each lab, if not each project. Analyzing these datasets in an efficient and open way is crucial for collaboration and reproducibility. In this combined webinar and tutorial, Adrien Peyrache and Guillaume Viejo will present Pynapple, a Python-based data analysis pipeline for systems neuroscience. Designed for flexibility and versatility, Pynapple allows users to perform cross-modal neural data analysis via a common programming approach which facilitates easy sharing of both analysis code and data.

In systems neuroscience, datasets are multimodal and include data-streams of various origins: multichannel electrophysiology, 1- or 2-p calcium imaging, behavior, etc. Often, the exact nature of data streams are unique to each lab, if not each project. Analyzing these datasets in an efficient and open way is crucial for collaboration and reproducibility. In this combined webinar and tutorial, Adrien Peyrache and Guillaume Viejo will present Pynapple, a Python-based data analysis pipeline for systems neuroscience. Designed for flexibility and versatility, Pynapple allows users to perform cross-modal neural data analysis via a common programming approach which facilitates easy sharing of both analysis code and data.

To generate brain circuits that are both flexible and stable requires the coordination of powerful developmental mechanisms acting at different scales, including activity-dependent synaptic plasticity and changes in single neuron properties. The brain prepares to efficiently compute information and reliably generate behavior during early development without any prior sensory experience but through patterned spontaneous activity. After the onset of sensory experience, ongoing activity continues to modify sensory circuits, and plays an important functional role in the mature brain. Using quantitative data analysis, experiment-driven theory and computational modeling, I will present a framework for how neural circuits are built and organized during early postnatal development into functional units, and how they are modified by intact and perturbed sensory-evoked activity. Inspired by experimental data from sensory cortex, I will then show how neural circuits use the resulting non-random connectivity to flexibly gate a network’s response, providing a mechanism for routing information.

Biological brains possess an exceptional ability to infer relevant behavioral responses to a wide range of stimuli from only a few examples. This capacity to generalize beyond the training set has been proven particularly challenging to realize in artificial systems. How neural processes enable this capacity to extrapolate to novel stimuli is a fundamental open question. A prominent but underexplored hypothesis suggests that generalization is facilitated by a low-dimensional organization of collective neural activity, yet evidence for the underlying neural mechanisms remains wanting. Combining network modeling, theory and neural data analysis, we tested this hypothesis in the framework of flexible timing tasks, which rely on the interplay between inputs and recurrent dynamics. We first trained recurrent neural networks on a set of timing tasks while minimizing the dimensionality of neural activity by imposing low-rank constraints on the connectivity, and compared the performance and generalization capabilities with networks trained without any constraint. We then examined the trained networks, characterized the dynamical mechanisms underlying the computations, and verified their predictions in neural recordings. Our key finding is that low-dimensional dynamics strongly increases the ability to extrapolate to inputs outside of the range used in training. Critically, this capacity to generalize relies on controlling the low-dimensional dynamics by a parametric contextual input. We found that this parametric control of extrapolation was based on a mechanism where tonic inputs modulate the dynamics along non-linear manifolds in activity space while preserving their geometry. Comparisons with neural recordings in the dorsomedial frontal cortex of macaque monkeys performing flexible timing tasks confirmed the geometric and dynamical signatures of this mechanism. Altogether, our results tie together a number of previous experimental findings and suggest that the low-dimensional organization of neural dynamics plays a central role in generalizable behaviors.

The ability to reach, grasp, and manipulate objects is a remarkable expression of motor skill, and the loss of this ability in injury, stroke, or disease can be devastating. These behaviors are controlled by the coordinated activity of tens of millions of neurons distributed across many CNS regions, including the primary motor cortex. While many studies have characterized the activity of single cortical neurons during reaching, the principles governing the dynamics of large, distributed neural populations remain largely unknown. Recent work in primates has suggested that during the execution of reaching, motor cortex may autonomously generate the neural pattern controlling the movement, much like the spinal central pattern generator for locomotion. In this seminar, I will describe recent work that tests this hypothesis using large-scale neural recording, high-resolution behavioral measurements, dynamical systems approaches to data analysis, and optogenetic perturbations in mice. We find, by contrast, that motor cortex requires strong, continuous, and time-varying thalamic input to generate the neural pattern driving reaching. In a second line of work, we demonstrate that the cortico-cerebellar loop is not critical for driving the arm towards the target, but instead fine-tunes movement parameters to enable precise and accurate behavior. Finally, I will describe my future plans to apply these experimental and analytical approaches to the adaptive control of locomotion in complex environments.

Entorhinal grid cells, so-called because of their hexagonally tiled spatial receptive fields, are organized in modules which, collectively, are believed to form a population code for the animal’s position. Here, we apply topological data analysis to simultaneous recordings of hundreds of grid cells and show that joint activity of grid cells within a module lies on a toroidal manifold. Each position of the animal in its physical environment corresponds to a single location on the torus, and each grid cell is preferentially active within a single “field” on the torus. Toroidal firing positions persist between environments, and between wakefulness and sleep, in agreement with continuous attractor models of grid cells.

Networks are widely used as mathematical models of complex systems across many scientific disciplines, and in particular within neuroscience. In this talk, we introduce two aspects of our collaborative research: (1) machine learning and networks, and (2) graph dimensionality. Machine learning and networks. Decades of work have produced a vast corpus of research characterising the topological, combinatorial, statistical and spectral properties of graphs. Each graph property can be thought of as a feature that captures important (and sometimes overlapping) characteristics of a network. We have developed hcga, a framework for highly comparative analysis of graph data sets that computes several thousands of graph features from any given network. Taking inspiration from hctsa, hcga offers a suite of statistical learning and data analysis tools for automated identification and selection of important and interpretable features underpinning the characterisation of graph data sets. We show that hcga outperforms other methodologies (including deep learning) on supervised classification tasks on benchmark data sets whilst retaining the interpretability of network features, which we exemplify on a dataset of neuronal morphologies images. Graph dimensionality. Dimension is a fundamental property of objects and the space in which they are embedded. Yet ideal notions of dimension, as in Euclidean spaces, do not always translate to physical spaces, which can be constrained by boundaries and distorted by inhomogeneities, or to intrinsically discrete systems such as networks. Deviating from approaches based on fractals, here, we present a new framework to define intrinsic notions of dimension on networks, the relative, local and global dimension. We showcase our method on various physical systems.

Remarkable advances in experimental neuroscience now enable us to simultaneously observe the activity of many neurons, thereby providing an opportunity to understand how the moment by moment collective dynamics of the brain instantiates learning and cognition. However, efficiently extracting such a conceptual understanding from large, high dimensional neural datasets requires concomitant advances in theoretically driven experimental design, data analysis, and neural circuit modeling. We will discuss how the modern frameworks of high dimensional statistics and deep learning can aid us in this process. In particular we will discuss: (1) how unsupervised tensor component analysis and time warping can extract unbiased and interpretable descriptions of how rapid single trial circuit dynamics change slowly over many trials to mediate learning; (2) how to tradeoff very different experimental resources, like numbers of recorded neurons and trials to accurately discover the structure of collective dynamics and information in the brain, even without spike sorting; (3) deep learning models that accurately capture the retina’s response to natural scenes as well as its internal structure and function; (4) algorithmic approaches for simplifying deep network models of perception; (5) optimality approaches to explain cell-type diversity in the first steps of vision in the retina.

Over the past years, genetic studies have uncovered hundreds of genetic variants to be associated with complex brain disorders. While this really represents a big step forward in understanding the genetic etiology of brain disorders, the functional interpretation of these variants remains challenging. We aim to help with the functional characterization of variants through transcriptomic data analysis. For instance, we rely on brain transcriptome atlases, such as Allen Brain Atlases, to infer functional relations between genes. One example of this is the identification of signaling mechanisms of steroid receptors. Further, by integrating brain transcriptome atlases with neuropathology and neuroimaging data, we identify key genes and pathways associated with brain disorders (e.g. Parkinson's disease). With technological advances, we can now profile gene expression in single-cells at large scale. These developments have presented significant computational developments. Our lab focuses on developing scalable methods to identify cells in single-cell data through interactive visualization, scalable clustering, classification, and interpretable trajectory modelling. We also work on methods to integrate single-cell data across studies and technologies.

In this talk I will present recent developments in data sharing, organization, and analyses that allow to build fully reproducible workflows. First, I will present the Brain Imaging Data structure and discuss how this allows to build workflows, showing some new tools to read/import/create studies from EEG data structured that way. Second, I will present several newly developed tools for reproducible pre-processing and statistical analyses. Although it does take some extra effort, I will argue that it largely feasible to make most EEG data analysis fully reproducible.

Remarkable advances in experimental neuroscience now enable us to simultaneously observe the activity of many neurons, thereby providing an opportunity to understand how the moment by moment collective dynamics of the brain instantiates learning and cognition.  However, efficiently extracting such a conceptual understanding from large, high dimensional neural datasets requires concomitant advances in theoretically driven experimental design, data analysis, and neural circuit modeling.  We will discuss how the modern frameworks of high dimensional statistics and deep learning can aid us in this process.  In particular we will discuss: how unsupervised tensor component analysis and time warping can extract unbiased and interpretable descriptions of how rapid single trial circuit dynamics change slowly over many trials to mediate learning; how to tradeoff very different experimental resources, like numbers of recorded neurons and trials to accurately discover the structure of collective dynamics and information in the brain, even without spike sorting; deep learning models that accurately capture the retina’s response to natural scenes as well as its internal structure and function; algorithmic approaches for simplifying deep network models of perception; optimality approaches to explain cell-type diversity in the first steps of vision in the retina.