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Amprimo, G.

Publications and source records attributed to Amprimo, G..

2 recordsLinked to original sources

Spike Train Scalograms (STS): a Deep Learning Classification Pipeline for Neuronal Cell Types

Classifying neuronal cell types is crucial for understanding the intricate circuitry of the cerebral cortex, which comprises diverse specialized neurons essential for brain function. Traditional Machine Learning (ML) approaches rely on manually engineered electrophysiological (EP) features, often overlooking subtle and complex patterns within spike train data. This study introduces a novel Spike Train Scalograms (STS)-based Deep Learning (DL) pipeline that integrates Continuous Wavelet Transform (CWT) scalograms with pre-trained Convolutional Neural Network (CNN) architectures to classify neuronal cell types with high accuracy. Utilizing patch-clamp EP recordings from 5,590 murine cortical neurons, the pipeline transforms spike trains into time-frequency representations via CWT, capturing both transient and sustained signal characteristics. These scalograms are then processed by fine-tuned CNN architectures, including InceptionV3, which achieved a balanced accuracy and weighted F1-Score of 90.53% and 90.03%, respectively. The STS pipeline effectively distinguishes between major neuronal types such as Pvalb, Sst, Vip/Lamp5, and Excitatory neurons, even in the presence of class imbalances. Moreover, an explainability analysis using saliency maps and SHAP revealed high correspondence between the DL approach, the ML baseline and biological knowledge of these neuronal types. The results demonstrate that, by combining an advanced spectral analysis with DL techniques, neurons can be classified with high accuracy, employing only two raw sweeps rather then the full stimulation range required by shallow approaches.

bioinformatics↗

Neuronal Spike Shapes (NSS): a simple approach to study electrophysiological data for heterogeneity investigation.

The mammalian brain exhibits a remarkable diversity of neurons, contributing to its intricate architecture and functional complexity. The analysis of multimodal single-cell datasets enables the investigation of cell types and states heterogeneity. In this study, we introduce the Neuronal Spike Shapes (NSS), a straightforward approach for the exploration of excitability states of neurons based on their Action Potential (AP) waveforms. The NSS method describes the AP waveform based on a triangular representation complemented by a set of derived electrophysiological (EP) features. To support this hypothesis, we validate the proposed approach on two datasets of murine cortical neurons, focusing it on GABAergic neurons. The validation process involves a combination of NSS-based clustering analysis, features exploration, Differential Expression (DE), and Gene Ontology (GO) enrichment analysis. Results show that the NSS-based analysis captures neuronal excitability states that possess biological relevance independently of cell subtype. In particular, Neuronal Spike Shapes (NSS) captures, among others, a well-characterized fast-spiking excitability state, supported by both electrophysiological and transcriptomic validation. Gene Ontology Enrichment Analysis reveals voltage-gated potassium (K+) channels as specific markers of the identified NSS partitions. This finding strongly corroborates the biological relevance of NSS partitions as excitability states, as the expression of voltage-gated K+ channels regulates the hyperpolarization phase of the AP, being directly implicated in the regulation of neuronal excitability.

bioengineering↗