Skip to content
Open access

Graph theory for the analysis of micro-electrode array recordings of human brain slices – framework and benchmarking

Aug 2026 · bioRxiv · 0 citations · 53 references
Biology

TL;DR

It is found that the method alone can change the apparent structure of the network as much as real biological differences do, and practical recommendations for parameter selection, reporting, and cross-method validation in MEA-based network neuroscience are provided.

Abstract

Micro-electrode array (MEA) recordings are widely used to characterize functional connectivity in neural cultures and have gained traction for the analysis of human brain slices. However, the impact of graph construction methodology on the resulting network topology has not been systematically quantified. Here, we benchmark three methods - shared spiking activity, Pearson cross-correlation, and the spike time tiling coefficient (STTC) - across 37 recordings from human cortical slice cultures classified into low, moderate, and high activity groups. We show that method choice alone produces large topological differences (Cohen’s d = 0.86–1.14 for clustering coefficient, d > 1.0 for node count), while higher-order features such as modularity remain stable. Each method exhibits a distinct sensitivity profile: shared spiking detects activity-dependent changes primarily through network size, correlation uniquely captures clustering differences, and STTC combines strong biological sensitivity with negligible parameter dependence across lag windows (all d < 0.1). Within shared spiking, z-score normalization dominates all other parameter choices (d > 1.0 versus bin size effects of d < 0.23), functioning as an implicit analytical null model that fundamentally reshapes the edge set rather than merely rescaling weights. Inter-method edge overlap is low (Jaccard index 0.08–0.45) and activity dependent, demonstrating that these methods identify substantially different connections from identical data. Our results reveal that methodological choices including construction method, threshold, and normalization introduce hidden degrees of freedom with effect sizes comparable to the biological signals being measured. We provide practical recommendations for parameter selection, reporting, and cross-method validation in MEA-based network neuroscience. Author Summary When we record electrical activity from brain tissue using grids of electrodes, we can ask how different sites influence one another and map the tissue as a network of connections. Thanks to novel culturing methods, this approach is increasingly used to study human brain slices. However, deciding what is “connected” is not well defined. Researchers use several different methods, and it has never been clear how much this choice shapes the network they end up describing. Here we compared three widely used methods on 37 recordings from human cortical slices spanning a range of activity levels. We found that the method alone can change the apparent structure of the network as much as real biological differences do. The methods frequently disagreed about which connections exist and some technical choices, including normalization techniques, had surprisingly large effects. Because these hidden choices can rival the biological signal, we provide this benchmarking work with practical recommendations for selecting, reporting, and cross-checking methods, so that network studies of brain tissue become more transparent, comparable, and reproducible.

Read PDF

Similar papers

Preprint Aug 2026

Graph Analysis of Neuronal-Culture Connectivity Derived from a Reservoir-Computing Model

This work presents an analytical pipeline for inferring network-level properties of in vitro cortical cultures from multichannel electrophysiological recordings and proves the validity of the RC-based connectivity inference and establishes a scalable, data-driven framework for functional network characterization in neuronal culture systems.

I. Auslender, G. Letti, Yasaman Heydari et al. · 0 citations
Open access Jul 2026

Brain space-time: graph neural fields capture multimodal spectra and functional properties of brain dynamics

I investigate a graph neural field model implemented on high-resolution multimodal individual human connectomes. The model, based on Wilson-Cowan and wave-diffusion equations, captures the harmonic power spectrum of functional magnetic resonance imaging (fMRI) and the temporal power spectrum of magnetoencephalography (MEG) over a wide range of scales. Additionally, the model displays properties of neuronal activity thought to be relevant for healthy brain function, such as proximity to instability and long-range temporal correlations (LRTCs), without being explicitly designed or optimized to achieve them. Finally, I find that model LRTCs originate in specific temporal frequency bands, display distinct patterns of spatial localization on the cortical surface, and are nontrivially linked to structural connectivity, with particular contributions of long-range white-matter fibers. Together, these findings extend the scope of graph neural fields as an effective framework for model-based investigations of multimodal neuroimaging data.

Marco Aqil · 0 citations
Open access Aug 2026

BRIDGE: A Computational Workflow from Single Neurons to Network of Mean-Field Models

BRIDGE provides a reproducible foundation for developing biologically informed mean-field models suitable for large-scale and whole-brain simulations, supporting the transition from generic homogeneous population models toward region-specific ones.

Ilaria Carannante, D. Depannemaecker, M. Woodman et al. · 0 citations
Open access Sep 2026

A network-based framework for detecting communities of similar neural spike trains

Recent advances in large-scale electrophysiological recording technologies now allow simultaneous measurement of spike trains from ensembles of neurons. A central challenge in mathematical neuroscience is therefore to identify functional assemblies and their collective organisation directly from this data. The goal of this work is to devise a method to infer the collective organisation of the neurons from their spiking activity. We construct weighted functional networks from neural spike trains using the van Rossum distance to quantify pairwise similarity. The functional network captures similarities in neuron firing patterns and provides a representation of their collective organisation. We hypothesise that similar neuronal assemblies will appear as clustered communities in the network, and employ the Louvain algorithm to detect such assemblies. We validate our approach using synthetic spike train data and simulated data from a stochastic block model of Leaky Integrate and Fire neurons subjected to external Poisson drives, where the ground truth is known. Finally, we apply our approach to large-scale recordings from the Allen Institute Visual Coding: Neuropixels dataset. We find that our methodology works well as long as a sufficient amount of data is available and the temporal structure is strong relative to the noise.

Unknown authors · 0 citations
Open access Aug 2026

Transcriptome-Inspired Spiking Simulations Uncover Human-Specific Prefrontal Dynamics and Provide a Mechanistic Platform for Species-Appropriate Disease Modeling

Whole-brain transcriptomic atlases are now widely available, yet computational neural models are almost exclusively parameterized from rodent data and used to infer human brain function, an extrapolation whose cost remains unquantified. To address this, we constructed a biophysically detailed, conductance-based Hodgkin–Huxley spiking microcircuit of a five-population prefrontal network, where every ion-channel, receptor, and gap-junction conductance was scaled by cell-type-specific gene expression. We parameterized the identical circuit using single-nucleus RNA-seq from mouse mPFC and human DLPFC, alongside a literature-derived baseline, and compared their high-frequency-oscillation (HFO) outputs across seven physiological and pathological states. While population firing rates differed only modestly between the two refinements (∼20% for pyramidal and PV cells), the oscillatory dynamics diverged dramatically. The human-refined circuit generated strongly synchronized PV activity and robust ripple- and fast-ripple-band power (e.g., healthy-wake ripple power, in arbitrary units: 322 vs. 24 and 22), whereas the mouse-refined and literature arms remained asynchronous (interneuron synchrony: 0.21 vs. 0.02). This human ≫mouse ≈ original hierarchy was statistically consistent across all seven states (significant arm differences in 75/77 comparisons). Mechanistically, the human transcriptome drove markedly stronger PV–PV electrical coupling (gap-junction scale: 1.78 vs. 0.96) paired with stronger recurrent pyramidal excitation, which collectively synchronized the fast-spiking PV population into a coherent rhythm that perisomatic inhibition then imposed on the local field potential. Critically, these results are model-dependent; the gene-to-conductance mapping is phenomenological, and mRNA expression does not linearly translate to functional conductance. Nonetheless, under this mapping the divergence localizes PV-mediated coupling and excitation–inhibition balance as the parameters most in need of human-specific recalibration. More broadly, this work establishes transcriptome-informed spiking simulation as a powerful strategy for uncovering species-specific computational principles and for building mechanistically grounded, human-relevant models of prefrontal circuit dysfunction, an approach that moves beyond generic rodent defaults to enable targeted, species-appropriate modeling of neurological and psychiatric disorders.

Qian-Quan Sun, Yihan Wang, Chunzhao Zhang · 0 citations
Open access Jul 2026

Emergent topological structure in spontaneous brain-organoid activity

Topological richness grows with network size, and second homology emerges significantly above the null only in the larger networks, and results show that persistent homology resolves structured topology in neural recordings at the scale experiments actually deliver.

Eve Bodnia, M. Basart, S. Hai et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.