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Aitor Morales-Gregorio

Publications and source records attributed to Aitor Morales-Gregorio.

3 recordsLinked to original sources

Geometric developmental principles for the emergence of brain-like weighted and directed neuronal networks

Brain networks exhibit remarkable structural properties, including high local clustering, short path lengths, and heavy-tailed weight and degree distributions. While these features are thought to enable efficient information processing with minimal wiring costs, the fundamental principles that generate such complex network architectures across species remain unclear. Here, we analyse single-neuron resolution connectomes across five species (C. Elegans, Platynereis, Drosophila M., zebrafish and mouse) to investigate the fundamental wiring principles underlying brain network formation. We show that distance-dependent connectivity alone produces small-world networks, but fails to generate heavy-tailed distributions. By incorporating weight-preferential attachment, which arises from spatial clustering of synapses along neurites, we reproduce heavy-tailed weight distributions while maintaining small-world topology. Adding degree-preferential attachment, linked to the extent of dendritic and axonal arborization, enables the generation of heavy-tailed degree distributions. Through systematic parameter exploration, we demonstrate that the combination of distance dependence, weight-preferential attachment, and degree-preferential attachment is sufficient to reproduce all characteristic properties of empirical brain networks. Our results reveal that activity-independent geometric constraints during neural development can account for the conserved architectural principles observed across evolutionarily distant species, suggesting universal mechanisms governing neural circuit assembly.

physics.bio-ph

Assessing the similarity of real matrices with arbitrary shape

Assessing the similarity of matrices is valuable for analyzing the extent to which data sets exhibit common features in tasks such as data clustering, dimensionality reduction, pattern recognition, group comparison, and graph analysis. Methods proposed for comparing vectors, such as cosine similarity, can be readily generalized to matrices. However, this approach usually neglects the inherent two-dimensional structure of matrices. Here, we propose singular angle similarity (SAS), a measure for evaluating the structural similarity between two arbitrary, real matrices of the same shape based on singular value decomposition. After introducing the measure, we compare SAS with standard measures for matrix comparison and show that only SAS captures the two-dimensional structure of matrices. Further, we characterize the behavior of SAS in the presence of noise and as a function of matrix dimensionality. Finally, we apply SAS to two use cases: square non-symmetric matrices of probabilistic network connectivity, and non-square matrices representing neural brain activity. For synthetic data of network connectivity, SAS matches intuitive expectations and allows for a robust assessment of similarities and differences. For experimental data of brain activity, SAS captures differences in the structure of high-dimensional responses to different stimuli. We conclude that SAS is a suitable measure for quantifying the shared structure of matrices with arbitrary shape.

q-bio.NC

Bringing Anatomical Information into Neuronal Network Models

For constructing neuronal network models computational neuroscientists have access to wide-ranging anatomical data that nevertheless tend to cover only a fraction of the parameters to be determined. Finding and interpreting the most relevant data, estimating missing values, and combining the data and estimates from various sources into a coherent whole is a daunting task. With this chapter we aim to provide guidance to modelers by describing the main types of anatomical data that may be useful for informing neuronal network models. We further discuss aspects of the underlying experimental techniques relevant to the interpretation of the data, list particularly comprehensive data sets, and describe methods for filling in the gaps in the experimental data. Such methods of `predictive connectomics' estimate connectivity where the data are lacking based on statistical relationships with known quantities. It is instructive, and in certain cases necessary, to use organizational principles that link the plethora of data within a unifying framework where regularities of brain structure can be exploited to inform computational models. In addition, we touch upon the most prominent features of brain organization that are likely to influence predicted neuronal network dynamics, with a focus on the mammalian cerebral cortex. Given the still existing need for modelers to navigate a complex data landscape full of holes and stumbling blocks, it is vital that the field of neuroanatomy is moving toward increasingly systematic data collection, representation, and publication.

q-bio.NC