TL;DR
This paper introduces a rapid, online algorithm for nonconvex deconvolution of calcium imaging data, significantly improving speed and accuracy over existing methods, and overcoming previous technical challenges.
Contribution
The authors develop a fast, online algorithm for calcium imaging deconvolution that is more efficient and avoids negative spikes, outperforming prior approaches.
Findings
Deconvolution of 100,000 timesteps in less than a second.
Superior performance on spikefinder challenge datasets.
Open-source implementation available for wider use.
Abstract
Calcium imaging data promises to transform the field of neuroscience by making it possible to record from large populations of neurons simultaneously. However, determining the exact moment in time at which a neuron spikes, from a calcium imaging data set, amounts to a non-trivial deconvolution problem which is of critical importance for downstream analyses. While a number of formulations have been proposed for this task in the recent literature, in this paper we focus on a formulation recently proposed in Jewell and Witten (2017) which has shown initial promising results. However, this proposal is slow to run on fluorescence traces of hundreds of thousands of timesteps. Here we develop a much faster online algorithm for solving the optimization problem of Jewell and Witten (2017) that can be used to deconvolve a fluorescence trace of 100,000 timesteps in less than a second.…
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