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Abu-Bonsrah, K. D.

Publications and source records attributed to Abu-Bonsrah, K. D..

3 recordsLinked to original sources

Handwritten Digit classification with neural cultures is influenced by neural architecture, network dynamics, and decoding methods

As silicon-based computing approaches fundamental physical limits, neurocomputing offers an energy-efficient alternative by leveraging the intrinsic non-linear dynamics of biological systems. To harness these dynamics, it is vital to understand the structure-function relationship governing how neural cultures process complex spatio-temporal information and how to appropriately decode the resulting neural electrophysiological activity. We investigated this utilizing a closed-loop electrophysiology platform, the CL1, to implement reservoir computing in human iPSC-derived neuronal networks. To systematically evaluate the variables driving neurocomputational capacity, we explored how cellular composition (cortical vs. hippocampal lineages), and the physical architecture (unstructured monolayers, 3D neural organoids, and modular networks confined by microfluidic devices) influenced electrophysiological properties and interacted with different decoding methodologies. Using a spatio-temporal version of a handwritten digit pattern recognition task (MNIST), we analyzed how these biological and analytical factors influenced classification accuracy. To ensure robust interpretation this required us to first demonstrated that reservoir computing decoding methods require strict artifact control and trial-based cross-validation to distinguish network computation from artifactual signal separability or temporal data leakage. Applying this validated frequency-domain pipeline, we suggest a clear functional hierarchy where structural modularity acts as a vital functional regularizer. Modular cortical cultures significantly outperformed unconstrained monolayers and organoids on MNIST. Furthermore, decoding frequency information from raw signals proved superior to typical time-bin decoding implementations. These findings establish that maximizing the computational potential of Synthetic Biological Intelligence, while avoiding false positives, requires a synergistic optimization of cellular identity, structural governance, and rigorous decoding logic. In doing so, this work provides a critical base establishing the criteria under which to evaluate neurocomputing implementations.

neuroscience↗

A novel protocol for the efficient generation of all three major hippocampal neuronal sub-populations from human pluripotent stem cells

The diverse computational functions of the human hippocampus rely on coordinated interactions among dentate gyrus (DG), CA3, and CA1 subfields, yet generating all three neuronal identities in vitro - particularly CA1 - has remained challenging. Here we establish a reproducible and modular differentiation protocol that directs human pluripotent stem cells (hPSCs) through dorsomedial telencephalic progenitors to yield DG, CA3, and CA1 neuronal subtypes together with hippocampal regionally specified astrocytes. Early tri-inhibition combined with Sonic hedgehog suppression produced dorsal forebrain progenitors (FOXG1+, PAX6+), while FGF2 treatment supported progenitor maintenance and induced TBR2+ intermediate progenitors. Controlled WNT activation using CHIR99021 drove progressive enrichment of PROX1 hippocampal progenitors across two independent donor lines. Terminal differentiation produced MAP2+/TAU+ neurons that expressed DG (PROX1), CA3 (GRIK4), and CA1 (WFS1, OCT6) markers, with maturing synaptic puncta. Defined progenitors generated long-lived (>400 days) hippocampal organoids exhibiting mixed neuronal-glial populations and spontaneous activity characterized by increased firing rates, high information entropy, and hub-like causal connectivity relative to monolayers, whereas astrocytes-supplemented monolayers displayed intermediate maturation. Population level electrophysiological analysis was also conducted to explore the dynamics of these different cultures. This platform enables systematic experimental control over neuron-astrocyte ratios, culture geometry, and developmental timing, providing a foundation for mechanistic studies of human hippocampal development, circuit function, and disease. Note on figure qualityThis is the preprint version of the manuscript. Figures are included adjacent to described results for the convenience of the reader but may be lower resolution due to file size restrictions on bioRxiv. High resolution figures are included as separate .tiff files for download.

neuroscience↗

Igniting full-length isoform analysis in single-cell and spatial RNA-seq data with FLAMESv2

Long-read single-cell RNA-sequencing enables the profiling of RNA isoform expression and alternative splicing at single cell resolution. However, diverse single-cell technologies and sparse isoform data demand flexible and accurate analysis tools. We introduce FLAMESv2, a highly modular and protocol-agnostic R/Bioconductor package for long-read single-cell RNA-seq data analysis. FLAMESv2 supports a wide range of single-cell and spatial protocols, is highly configurable, scales to allow multi-sample analysis and provides versatile visualisation and analysis outputs. We demonstrate its compatibility with both droplet-based and combinatorial barcoding single-cell methods, as well as spatial transcriptomics workflows. Benchmarking confirms FLAMESv2 achieves field-leading performance across key analysis tasks. Applying FLAMESv2 to in vitro differentiation of stem cells into neurons, we identify cell-types, differentiation trajectories, expression of annotated and novel isoforms and isoform expression diversity and heterogeneity within individual cells. FLAMESv2 provides a comprehensive, flexible approach to analysing long-read single-cell RNA-sequencing, unlocking this powerful methodology for RNA isoform characterisation.

bioinformatics↗