Abstract

Objective. Inferring the times of sequences of action potentials (APs) (spike trains) from neurophysiological data is a key problem in computational neuroscience. The detection of APs from two-photon imaging of calcium signals offers certain advantages over traditional electrophysiological approaches, as up to thousands of spatially and immunohistochemically defined neurons can be recorded simultaneously. However, due to noise, dye buffering and the limited sampling rates in common microscopy configurations, accurate detection of APs from calcium time series has proved to be a difficult problem. Approach. Here we introduce a novel approach to the problem making use of finite rate of innovation (FRI) theory (Vetterli et al 2002 IEEE Trans. Signal Process. 50 1417–28). For calcium transients well fit by a single exponential, the problem is reduced to reconstructing a stream of decaying exponentials. Signals made of a combination of exponentially decaying functions with different onset times are a subclass of FRI signals, for which much theory has recently been developed by the signal processing community. Main results. We demonstrate for the first time the use of FRI theory to retrieve the timing of APs from calcium transient time series. The final algorithm is fast, non-iterative and parallelizable. Spike inference can be performed in real-time for a population of neurons and does not require any training phase or learning to initialize parameters. Significance. The algorithm has been tested with both real data (obtained by simultaneous electrophysiology and multiphoton imaging of calcium signals in cerebellar Purkinje cell dendrites), and surrogate data, and outperforms several recently proposed methods for spike train inference from calcium imaging data.

Highlights

  • Understanding how information processing occurs in neural circuits is one of the principal problems of systems neuroscience

  • To understand neural information processing, we must monitor the activity of neural circuits at a spatial resolution sufficient to resolve many individual neurons, and a temporal resolution sufficient to resolve individual action potentials (APs) on individual experimental trials

  • To investigate information processing in neural circuits, it is necessary to relate these calcium signals to the properties of the spike trains fired by the neurons, ideally by detecting the times of occurrence of spikes with single AP resolution

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Summary

Introduction

Understanding how information processing occurs in neural circuits is one of the principal problems of systems neuroscience. Populations of neurons can be simultaneously labelled with acetoxy-methyl (AM) ester calcium dyes (Stosiek et al 2003), allowing simultaneous monitoring of AP induced calcium signals in a plane (Ohki et al 2005) or volume (Göbel and Helmchen 2007) of tissue. To investigate information processing in neural circuits, it is necessary to relate these calcium signals to the properties of the spike trains fired by the neurons, ideally by detecting the times of occurrence of spikes with single AP resolution. A number of methods have previously been used to detect spike trains from calcium imaging data, including thresholding the first derivative of the calcium signal (Smetters et al 1999), and the application of template-matching algorithms based on either fixed exponential (Kerr et al 2005, 2007, Greenberg et al 2008) or data-derived (Schultz et al 2009, Ozden et al 2008) templates. Machine learning techniques (Sasaki et al 2008) and probabilistic methods based on sequential Monte Carlo framework (Vogelstein et al 2009) or fast deconvolution (Vogelstein et al 2010) have been proposed

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