Deep Neuron Embeddings: Data-driven multi-modal discovery of cell types in the neocortex
This project aims to link the morphology and function of excitatory cortical neurons using machine learning to create a "bar code" for neuron classification, enhancing our understanding of brain diversity.
Projectdetails
Introduction
Understanding the relationship between structure and function of cortical neurons and circuits is one of the key challenges in neuroscience. For inhibitory neurons, roughly 15 subtypes are well characterized and we know a fair bit about their function. However, the vast majority of neocortical neurons are excitatory.
Research Gap
Yet we know little about how differences in the morphology of excitatory neurons relate to their computational properties in vivo. I hypothesize that there is a close correspondence between morphology and function of excitatory neurons: distinct subtypes can be identified not only by their morphological features, but also by how they respond to stimulation with natural stimuli.
Methodology
To test this hypothesis, I will build upon recent advances in machine learning and develop a data-driven approach to derive a "bar code" for each neuron: a low-dimensional representation of its morphological features and its response properties to natural stimuli.
Data Source
Using these techniques, I will tackle the structure-function question by harnessing a large-scale functional anatomy dataset: a combination of electron-microscopy reconstructions at sub-micrometer resolution with two-photon functional imaging of nearly all excitatory neurons in one cubic millimeter of the mouse visual cortex.
Potential Impact
If successful, my project could fundamentally change our view on the diversity of excitatory cell types and reveal how morphological features are linked to a neuron's computational output. It could pave the way towards a unified definition of cell types, one of the fundamental building blocks of the brain.
Broader Applications
The same approach could be used in other brain areas and even other cellular systems beyond the brain. More broadly, while machine learning is promising to transform the scientific discovery process as a whole, my project could serve as a prime example of this transformation process in neuroscience and show how machine learning can help to discover structure in nature.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.500.000 |
Totale projectbegroting | € 1.500.000 |
Tijdlijn
Startdatum | 1-6-2022 |
Einddatum | 31-5-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- GEORG-AUGUST-UNIVERSITAT GOTTINGEN STIFTUNG OFFENTLICHEN RECHTSpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
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Next generation mechanistic models of retinal interneurons
This project aims to develop hybrid mechanistic models of retinal amacrine cells, integrating machine learning and imaging data to uncover their roles in visual computations and link them to genetic types.
Using deep learning to understand computations in neural circuits with Connectome-constrained Mechanistic Models
This project aims to develop a machine learning framework that integrates mechanistic modeling and deep learning to understand neural computations in Drosophila melanogaster's circuits.
A novel theory of human cortical microcircuit function: Dedicated neuronal networks for fast cellular and synaptic computation
This project aims to uncover the mechanisms behind fast input-output properties of human-specialized neuron types and their role in cognition and cognitive decline using advanced neurobiological techniques.
A unifying dynamical theory of distributed computation and generalisation in biological and artificial neural systems
This project aims to develop a mathematical framework to model global brain dynamics and infer invariant representations from local neural recordings, enhancing understanding of cognitive processes and machine learning.
Deciphering the Regulatory Logic of Cortical Development
EpiCortex aims to map the regulatory landscape of mouse cortical development across timepoints to understand neuronal lineage specification and improve therapeutic strategies for neuropsychiatric diseases.