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Vestergaard, C. L.

Publications and source records attributed to Vestergaard, C. L..

3 recordsLinked to original sources

Statistical signature of subtle behavioural changes inlarge-scale behavioural assays

The central nervous system can generate various behaviours, including motor responses, which we can observe through video recordings. Recent advancements in genetics, automated behavioural acquisition at scale, and machine learning enable us to link behaviours to their underlying neural mechanisms causally. Moreover, in some animals, such as the Drosophila larva, this mapping is possible at unprecedented scales of millions of animals and single neurons, allowing us to identify the neural circuits generating particular behaviours. These high-throughput screening efforts are invaluable, linking the activation or suppression of specific neurons to behavioural patterns in millions of animals. This provides a rich dataset to explore how diverse nervous system responses can be to the same stimuli. However, challenges remain in identifying subtle behaviours from these large datasets, including immediate and delayed responses to neural activation or suppression, and understanding these behaviours on a large scale. We introduce several statistically robust methods for analyzing behavioural data in response to these challenges: 1) A generative physical model that regularizes the inference of larval shapes across the entire dataset. 2) An unsupervised kernel-based method for statistical testing in learned behavioural spaces aimed at detecting subtle deviations in behaviour. 3) A generative model for larval behavioural sequences, providing a benchmark for identifying complex behavioural changes. 4) A comprehensive analysis technique using suffix trees to categorize genetic lines into clusters based on common action sequences. We showcase these methodologies through a behavioural screen focused on responses to an air puff, analyzing data from 280,716 larvae across 568 genetic lines. Author SummaryThere is a significant gap in understanding between the architecture of neural circuits and the mechanisms of action selection and behaviour generation.Drosophila larvae have emerged as an ideal platform for simultaneously probing behaviour and the underlying neuronal computation [1]. Modern genetic tools allow efficient activation or silencing of individual and small groups of neurons. Combining these techniques with standardized stimuli over thousands of individuals makes it possible to relate neurons to behaviour causally. However, extracting these relationships from massive and noisy recordings requires the development of new statistically robust approaches. We introduce a suite of statistical methods that utilize individual behavioural data and the overarching structure of the behavioural screen to deduce subtle behavioural changes from raw data. Given our studys extensive number of larvae, addressing and preempting potential challenges in body shape recognition is critical for enhancing behaviour detection. To this end, we have adopted a physics-informed inference model. Our first group of techniques enables robust statistical analysis within a learned continuous behaviour latent space, facilitating the detection of subtle behavioural shifts relative to reference genetic lines. A second array of methods probes for subtle variations in action sequences by comparing them to a bespoke generative model. Together, these strategies have enabled us to construct representations of behavioural patterns specific to a lineage and identify a roster of "hit" neurons with the potential to influence behaviour subtly.

neuroscience↗

LarvaTagger: Manual and automatic tagging of Drosophila larval behaviour

MotivationAs more behavioural assays are carried out in large-scale experiments on Drosophila larvae, the definitions of the archetypal actions of a larva are regularly refined. In addition, video recording and tracking technologies constantly evolve. Consequently, automatic tagging tools for Drosophila larval behaviour must be retrained to learn new representations from new data. However, existing tools cannot transfer knowledge from large amounts of previously accumulated data. We introduce LarvaTagger, a piece of software that combines a pre-trained deep neural network, providing a continuous latent representation of larva actions for stereotypical behaviour identification, with a graphical user interface to manually tag the behaviour and train new automatic taggers with the updated ground truth. ResultsWe reproduced results from an automatic tagger with high accuracy, and we demonstrated that pre-training on large databases accelerates the training of a new tagger, achieving similar prediction accuracy using less data. AvailabilityAll the code is free and open source. Docker images are also available. See git-lab.pasteur.fr/nyx/LarvaTagger.jl.

bioinformatics↗

A maximum mean discrepancy approach reveals subtle changes in α-synuclein dynamics

Numerous models have been developed to account for the complex properties of the random walks of biomolecules. However, when analysing experimental data, conditions are rarely met to ensure model identification. The dynamics may simultaneously be influenced by spatial and temporal heterogeneities of the environment, out-of-equilibrium fluxes and conformal changes of the tracked molecules. Recorded trajectories are often too short to reliably discern such multi-scale dynamics, which precludes unambiguous assessment of the type of random walk and its parameters. Furthermore, the motion of biomolecules may not be well described by a single, canonical random walk model. Here, we develop a methodology for comparing biomolecule dynamics observed in different experimental conditions without beforehand identifying the model generating the recorded random walks. We introduce a two-step statistical testing scheme. We first use simulation-based inference to train a graph neural network to learn a fixed-length latent representation of recorded random walks. As a second step, we use a maximum mean discrepancy statistical test on the vectors of learnt features to compare biological conditions. This procedure allows us to characterise sets of random walks regardless of their generating models. We initially tested our approach on numerical trajectories. We then demonstrated its ability to detect changes in -synuclein dynamics at synapses in cultured cortical neurons in response to membrane depolarisation. Using our methodology, we identify the domains in the latent space where the variations between conditions are the most significant, which provides a way of interpreting the detected differences in terms of single trajectory characteristics. Our data show that changes in -synuclein dynamics between the chosen conditions are largely driven by increased protein mobility in the depolarised state. Author summaryThe continuous refinement of methods for single molecule tracking in live cells advance our understanding of how biomolecules move inside cells. Analysing the trajectories of single molecules is complicated by their highly erratic and noisy nature and thus requires the use of statistical models of their motion. However, it is often not possible to unambiguously determine a model from a set of short and noisy trajectories. Furthermore, the heterogeneous nature of the cellular environment means that the molecules motion is often not properly described by a single model. In this paper we develop a new statistical testing scheme to detect changes in biomolecule dynamics within organelles without needing to identify a model of their motion. We train a graph neural network on large-scale simulations of random walks to learn a latent representation that captures relevant physical properties of a trajectory. We use a kernel-based statistical test within that latent space to compare the properties of two sets of trajectories recorded under different biological conditions. We apply our approach to detect differences in the dynamics of -synuclein, a presynaptic protein, in axons and boutons during synaptic stimulation. This represents an important step towards automated single-molecule-based read-out of pharmacological action.

biophysics↗