Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Sparse component analysis: A method that uncovers separable computations within neural population activity.

Neuron·2026
Same author

Beast3D: Animal behavioral analysis and neural encoding from multi-view video via Gaussian splatting.

ArXiv·2026
Same author

Lightning Pose 3D: an uncertainty-aware framework for data-efficient multi-view animal pose estimation.

bioRxiv : the preprint server for biology·2026
Same author

Statistically valid explainable black-box machine learning: applications in sex classification across species using brain imaging.

PloS one·2026
Same author

Computational optimization of two-photon holographic stimulation sites<i>in vivo</i>.

Journal of neural engineering·2026
Same author

Animal behavioral analysis and neural encoding with transformer-based self-supervised pretraining.

ArXiv·2026

Related Experiment Video

Updated: Jun 12, 2026

Optical Recording of Suprathreshold Neural Activity with Single-cell and Single-spike Resolution
08:48

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

Published on: September 5, 2012

Fast nonnegative deconvolution for spike train inference from population calcium imaging.

Joshua T Vogelstein1, Adam M Packer, Timothy A Machado

  • 1Johns Hopkins University, Department of Neuroscience, 3400 N. Charles St., Baltimore, MD 21205, USA. joshuav@jhu.edu

Journal of Neurophysiology
|June 18, 2010
PubMed
Summary

This study introduces a fast nonnegative deconvolution filter for inferring neuronal spiking activity from calcium imaging data. This new method outperforms traditional Wiener filtering, enabling real-time analysis of large neuronal populations.

More Related Videos

Calcium Imaging In Electrically Stimulated Flat-Mounted Retinas
07:25

Calcium Imaging In Electrically Stimulated Flat-Mounted Retinas

Published on: August 18, 2023

Imaging Calcium Dynamics in Subpopulations of Mouse Pancreatic Islet Cells
08:03

Imaging Calcium Dynamics in Subpopulations of Mouse Pancreatic Islet Cells

Published on: November 26, 2019

Related Experiment Videos

Last Updated: Jun 12, 2026

Optical Recording of Suprathreshold Neural Activity with Single-cell and Single-spike Resolution
08:48

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

Published on: September 5, 2012

Calcium Imaging In Electrically Stimulated Flat-Mounted Retinas
07:25

Calcium Imaging In Electrically Stimulated Flat-Mounted Retinas

Published on: August 18, 2023

Imaging Calcium Dynamics in Subpopulations of Mouse Pancreatic Islet Cells
08:03

Imaging Calcium Dynamics in Subpopulations of Mouse Pancreatic Islet Cells

Published on: November 26, 2019

Area of Science:

  • Neuroscience
  • Computational Biology
  • Signal Processing

Background:

  • Fluorescent calcium indicators are widely used to monitor neuronal activity.
  • Extracting precise spike trains from fluorescence data is challenging.

Purpose of the Study:

  • To develop a fast and accurate algorithm for inferring neuronal spike trains from fluorescence imaging data.
  • To improve upon existing deconvolution methods for calcium imaging analysis.

Main Methods:

  • A fast nonnegative deconvolution filter was developed, utilizing an interior-point method for positivity constraints.
  • The algorithm was tested on simulated and biological data, and spatial filtering was applied.
  • Parameter estimation was performed solely using fluorescence data, eliminating the need for joint calibration.

Main Results:

  • The nonnegative deconvolution filter significantly outperformed optimal linear deconvolution (Wiener filtering).
  • The algorithm operates in linear time, allowing for faster-than-real-time inference even with large neuronal populations (>100 neurons).
  • Spatial filtering further enhanced the accuracy of inferred spike trains.

Conclusions:

  • The developed nonnegative deconvolution filter provides a robust and efficient method for analyzing neuronal spiking activity.
  • This approach simplifies experimental workflows by removing the need for joint electrophysiological and imaging calibration.
  • The algorithm facilitates high-throughput analysis of large-scale neuronal population dynamics.