Spike Data Processing

Spike data processing is the computational analysis of neuronal action-potential recordings to convert raw voltage or extracellular signals into interpretable measures of neural activity. It typically involves filtering noise, detecting waveform events, sorting spikes by waveform or recording source, and extracting features such as firing rate, timing, and interspike intervals. In neuroscience, these steps help researchers distinguish activity from individual neurons, characterize population dynamics, and relate neural firing to stimuli, behavior, or disease. Reliable processing supports electrophysiology, brain-computer interfaces, and models of neural coding, while careful parameter selection and validation reduce missed spikes, false detections, and sorting errors.

Spike Data Processing - Related Videos

Research

JoVE EoE - Neurophysiology

Triggering a Closed-Loop Stimulation by Neuron Spiking Activity

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2025

This video demonstrates the operation of closed-loop stimulation in a rat with a surgically implanted device to record neural activity. Neuronal signals are first recorded and analyzed. Template waveforms are then uploaded, and parameters are defined to trigger closed-loop stimulation.

Research

JoVE Journal - Immunology and Infection
Free Sample

Averaging of Viral Envelope Glycoprotein Spikes from Electron Cryotomography Reconstructions using Jsubtomo

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Cited by 23 •

2014

An approach is presented for determining structures of viral membrane glycoprotein complexes using a combination of electron cryo-tomography and sub-tomogram averaging with the computational package Jsubtomo.

Optical Recording of Suprathreshold Neural Activity with Single-cell and Single-spike Resolution

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Cited by 1 •

2012

Understanding the function of the vertebrate central nervous system requires recordings from many neurons because cortical function arises on the level of populations of neurons. Here we describe an optical method to record suprathreshold neural activity with single-cell and single-spike resolution, dithered random-access scanning. This method records somatic fluorescence calcium signals from up to 100 neurons with high temporal resolution. A maximum-likelihood algorithm deconvolves the...

A Simple Stimulatory Device for Evoking Point-like Tactile Stimuli: A Searchlight for LFP to Spike Transitions

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Cited by 4 •

2014

To elucidate the complex transition from Local Field Potentials (LFPs) to spikes a suitable stimulator for light mechanical peripheral stimuli was built. As an application, the spiking activities recorded from somatosensory cortex were analyzed by a multi-objective optimization strategy. The results demonstrated that the proposed stimulator was able to deliver tactile stimuli with millisecond and millimeter precisions.

Visualizing Dose-Dependent Spike Protein Uptake with Quantum Dot Conjugates

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2026

Source: Tran, B. N., et. al. High-throughput Confocal Imaging of Quantum Dot-Conjugated SARS-CoV-2 Spike Trimers to Track Binding and Endocytosis in HEK293T Cells. J. Vis. Exp. (2022)This video demonstrates the use of quantum dot–conjugated spike protein (QD-Spike) to visualize dose-dependent viral entry in ACE2-GFP–expressing cells. Confocal imaging captures the internalization of QD-Spike via receptor-mediated endocytosis, modeling early coronavirus entry.

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