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      Deconvolution of calcium imaging data using marked point processes

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      1 , 2 , 3 , 4 , *
      PLoS Computational Biology
      Public Library of Science

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          Abstract

          Calcium imaging has been widely used for measuring spiking activities of neurons. When using calcium imaging, we need to extract summarized information from the raw movie beforehand. Recent studies have used matrix deconvolution for this preprocessing. However, such an approach can neither directly estimate the generative mechanism of spike trains nor use stimulus information that has a strong influence on neural activities. Here, we propose a new deconvolution method for calcium imaging using marked point processes. We consider that the observed movie is generated from a probabilistic model with marked point processes as hidden variables, and we calculate the posterior of these variables using a variational inference approach. Our method can simultaneously estimate various kinds of information, such as cell shape, spike occurrence time, and tuning curve. We apply our method to simulated and experimental data to verify its performance.

          Author summary

          Calcium imaging is a promising technique that enables the observation of the activities of large neural populations as a movie. Since the measured movie is a large-scale dataset containing a considerable amount of information, we need to apply a preprocessing procedure to extract crucial information from the raw movie for the analysis that follows. Recent studies have adopted matrix decomposition to decompose the observed movie into the product of two matrices: one consisting of cell shapes and the other consisting of calcium florescent time series. This approach can estimate cell locations and activities simultaneously; however, it cannot express some aspects of neural population codes. For instance, this approach cannot incorporate other covariates that may affect the neural population activities. In this paper, we propose a new statistical model for calcium imaging movies and an estimation procedure for this model. To express the random occurrence of spikes occurring in the movie, our model adopts a marked point process, which is used to express sequences of events to which certain characteristic values are attached. Our model can estimate cell shapes, spikes, and tuning curves of cells directly without any additional preprocessing procedure, and it also improves the estimation accuracy compared to the conventional approach.

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          Graphical Models, Exponential Families, and Variational Inference

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            Simultaneous Denoising, Deconvolution, and Demixing of Calcium Imaging Data.

            We present a modular approach for analyzing calcium imaging recordings of large neuronal ensembles. Our goal is to simultaneously identify the locations of the neurons, demix spatially overlapping components, and denoise and deconvolve the spiking activity from the slow dynamics of the calcium indicator. Our approach relies on a constrained nonnegative matrix factorization that expresses the spatiotemporal fluorescence activity as the product of a spatial matrix that encodes the spatial footprint of each neuron in the optical field and a temporal matrix that characterizes the calcium concentration of each neuron over time. This framework is combined with a novel constrained deconvolution approach that extracts estimates of neural activity from fluorescence traces, to create a spatiotemporal processing algorithm that requires minimal parameter tuning. We demonstrate the general applicability of our method by applying it to in vitro and in vivo multi-neuronal imaging data, whole-brain light-sheet imaging data, and dendritic imaging data.
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              Long-term dynamics of CA1 hippocampal place codes

              Via Ca2+-imaging in freely behaving mice that repeatedly explored a familiar environment, we tracked thousands of CA1 pyramidal cells' place fields over weeks. Place coding was dynamic, for each day the ensemble representation of this environment involved a unique subset of cells. Yet, cells within the ∼15–25% overlap between any two of these subsets retained the same place fields, which sufficed to preserve an accurate spatial representation across weeks.
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                Author and article information

                Contributors
                Role: InvestigationRole: SoftwareRole: Writing – original draftRole: Writing – review & editing
                Role: InvestigationRole: SupervisionRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput. Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, CA USA )
                1553-734X
                1553-7358
                March 2020
                12 March 2020
                : 16
                : 3
                : e1007650
                Affiliations
                [1 ] NTT Communication Science Laboratories, Atsugi-shi, Japan
                [2 ] Department of Mathematical Informatics, The University of Tokyo, Tokyo, Japan
                [3 ] RIKEN Center for Brain Science, Wako-shi, Japan
                [4 ] International Research Center for Neurointelligence (IRCN), The University of Tokyo, Tokyo, Japan
                University of Toronto at Scarborough, CANADA
                Author notes

                The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0001-8371-5092
                Article
                PCOMPBIOL-D-19-00443
                10.1371/journal.pcbi.1007650
                7093033
                32163407
                abaaf37a-7761-4fec-9002-462b4c5913ac
                © 2020 Shibue, Komaki

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 19 March 2019
                : 10 January 2020
                Page count
                Figures: 11, Tables: 0, Pages: 25
                Funding
                This work (FK) was supported by MEXT KAKENHI Grant number 16H06533 (Ministry of Education, Culture, Sports, Science and Technology, http://www.mext.go.jp/en/), JST CREST Grant Number JPMJCR1763 (Japan Science and Technology Agency, http://www.jst.go.jp/EN/), and AMED Grant Numbers JP19dm0207001 and JP18dm0307009 (Japan Agency for Medical Research and Development, https://www.amed.go.jp/en/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Neurons
                Biology and Life Sciences
                Neuroscience
                Cellular Neuroscience
                Neurons
                Research and Analysis Methods
                Imaging Techniques
                Neuroimaging
                Calcium Imaging
                Biology and Life Sciences
                Neuroscience
                Neuroimaging
                Calcium Imaging
                Biology and Life Sciences
                Neuroscience
                Neuronal Tuning
                Research and Analysis Methods
                Imaging Techniques
                Fluorescence Imaging
                Biology and Life Sciences
                Physiology
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                Membrane Potential
                Action Potentials
                Medicine and Health Sciences
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                Electrophysiology
                Membrane Potential
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                Biology and Life Sciences
                Physiology
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                Neurophysiology
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                Medicine and Health Sciences
                Physiology
                Electrophysiology
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                Action Potentials
                Biology and Life Sciences
                Neuroscience
                Neurophysiology
                Action Potentials
                Computer and Information Sciences
                Software Engineering
                Preprocessing
                Engineering and Technology
                Software Engineering
                Preprocessing
                Physical Sciences
                Mathematics
                Operator Theory
                Kernel Functions
                Research and Analysis Methods
                Animal Studies
                Experimental Organism Systems
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                Research and Analysis Methods
                Model Organisms
                Mouse Models
                Research and Analysis Methods
                Animal Studies
                Experimental Organism Systems
                Animal Models
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                Custom metadata
                vor-update-to-uncorrected-proof
                2020-03-24
                Data are available at CodeNeuro: http://neurofinder.codeneuro.org/.

                Quantitative & Systems biology
                Quantitative & Systems biology

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