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Harth, P.

Publications and source records attributed to Harth, P..

4 recordsLinked to original sources

MoMo - Combining Neuron Morphology and Connectivity forInteractive Motif Analysis in Connectomes

Connectomics, a subfield of neuroscience, reconstructs structural and functional brain maps at synapse-level resolution. These complex spatial maps consist of tree-like neurons interconnected by synapses. Motif analysis is a widely used method for identifying recurring subgraph patterns in connectomes. These motifs, thus, potentially represent fundamental units of information processing. However, existing computational tools often oversimplify neurons as mere nodes in a graph, disregarding their intricate morphologies. In this paper, we introduce MoMo, a novel interactive visualization framework for analyzing neuron morphology-aware motifs in large connectome graphs. First, we propose an advanced graph data structure that integrates both neuronal morphology and synaptic connectivity. This enables highly efficient, parallel subgraph isomorphism searches, allowing for interactive morphological motif queries. Second, we develop a sketch-based interface that facilitates the intuitive exploration of morphology-based motifs within our new data structure. Users can conduct interactive motif searches on state-of-the-art connectomes and visualize results as interactive 3D renderings. We present a detailed goal and task analysis for motif exploration in connectomes, incorporating neuron morphology. Finally, we evaluate MoMo through case studies with four domain experts, who asses the tools usefulness and effectiveness in motif exploration, and relevance to real-world neuroscience research. The source code for MoMo is available here.

neuroscience↗

Dissecting origins of wiring specificity in dense cortical connectomes

What are the origins of the highly specific wiring patterns that are formed by the neurons in the brain? To address this question, we introduce a method to predict the empirically observed wiring diagram - the connectome - at synaptic resolution based on dense electron-microscopic reconstructions of neural tissue. Our method generates the connectome based on the morphological properties of the neurons in combination with synaptic specificity models, whose parameters capture how neurons wire conditional on their subcellular, cellular and cell type properties. We employ simulation-based Bayesian inference to identify all values for these parameters that can generate the observed connectome. Finally, for each synapse in a dense reconstruction, our method provides quantitative measures to reveal which synaptic specificity models are necessary, sufficient and best-suited to generate it. The output of our method are experimentally testable predictions of wiring preferences from subcellular to cell type levels that could account for each synapse in dense reconstructions. We demonstrate our method on dense datasets from mouse primary visual and human temporal cortex. Strikingly, this demonstration shows that just three assumptions, with nearly the same synaptic specificity values, predict the connectivity in both datasets. Our method is openly accessible as a computational framework that includes a comprehensive workflow for the analysis of wiring specificity, and which provides users with full flexibility to define and test their hypotheses. Our method sets the stage to uncover the principles by which neural networks are organized, and to compare these principles across brain areas, species and time points.

neuroscience↗

Simulation-based inference for efficient identification of generative models in connectomics

Recent advances in connectomics research enable the acquisition of increasing amounts of data about the connectivity patterns of neurons. How can we use this wealth of data to efficiently derive and test hypotheses about the principles underlying these patterns? A common approach is to simulate neuronal networks using a hypothesized wiring rule in a generative model and to compare the resulting synthetic data with empirical data. However, most wiring rules have at least some free parameters, and identifying parameters that reproduce empirical data can be challenging as it often requires manual parameter tuning. Here, we propose to use simulation-based Bayesian inference (SBI) to address this challenge. Rather than optimizing a fixed wiring rule to fit the empirical data, SBI considers many parametrizations of a rule and performs Bayesian inference to identify the parameters that are compatible with the data. It uses simulated data from multiple candidate wiring rule parameters and relies on machine learning methods to estimate a probability distribution (the posterior distribution over parameters conditioned on the data) that characterizes all data-compatible parameters. We demonstrate how to apply SBI in computational connectomics by inferring the parameters of wiring rules in an in silico model of the rat barrel cortex, given in vivo connectivity measurements. SBI identifies a wide range of wiring rule parameters that reproduce the measurements. We show how access to the posterior distribution over all data-compatible parameters allows us to analyze their relationship, revealing biologically plausible parameter interactions and enabling experimentally testable predictions. We further show how SBI can be applied to wiring rules at different spatial scales to quantitatively rule out invalid wiring hypotheses. Our approach is applicable to a wide range of generative models used in connectomics, providing a quantitative and efficient way to constrain model parameters with empirical connectivity data. Author summaryThe brain is composed of an intricately connected network of cells--what are the principles that contribute to constructing these patterns of connectivity, and how? To answer these questions, amassing connectivity data alone is not enough. We must also be able to efficiently develop and test our ideas about the underlying connectivity principles. For example, we could simulate a hypothetical wiring rule like "neurons near each other are more likely to form connections" in a computational model and generate corresponding synthetic data. If the synthetic, simulated data resembles the real, measured data, then we have some confidence that our hypotheses might be correct. However, the proposed wiring rules usually have unknown parameters that we need to "tune" such that simulated data matches the measurements. The central challenge thus lies in finding all the potential parametrizations of a wiring rule that can reproduce the measured data, as this process is often idiosyncratic and labor-intensive. To tackle this challenge, we introduce an approach combining computational modeling in connectomics, deep learning, and Bayesian statistical inference to automatically infer a probability distribution over the model parameters likely to explain the data. We demonstrate our approach by inferring the parameters of a wiring rule in a detailed model of the rat barrel cortex and find that the inferred distribution identifies multiple data-compatible model parameters, reveals biologically plausible parameter interactions, and allows us to make experimentally testable predictions.

neuroscience↗

A Theory for the Emergence of Neocortical Network Architecture

It has become increasingly clear that the neurons in the cerebral cortex are not randomly interconnected. This wiring specificity can result from synapse formation mechanisms that interconnect neurons depending on their activity or genetically defined identity. Here we report that in addition to these synapse formation mechanisms, the structural composition of the neuropil provides a third prominent source by which wiring specificity emerges in cortical networks. This structurally determined wiring specificity reflects the packing density, morphological diversity and similarity of the dendritic and axonal processes. The higher these three factors are, the more recurrent the topology of the networks. Conversely, low density, diversity and similarity yield feedforward networks. These principles predict connectivity patterns from subcellular to network scales that are remarkably consistent with empirical observations from a rich body of literature. Thus, cortical network architectures reflect the specific morphological properties of their constituents to much larger degrees than previously thought.

neuroscience↗