Deconvolution of Sustained Neural Activity From Large-Scale Calcium Imaging Data

2020 ◽  
Vol 39 (4) ◽  
pp. 1094-1103
Author(s):  
Younes Farouj ◽  
Fikret Isik Karahanoglu ◽  
Dimitri Van De Ville
eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Markus Frey ◽  
Sander Tanni ◽  
Catherine Perrodin ◽  
Alice O'Leary ◽  
Matthias Nau ◽  
...  

Rapid progress in technologies such as calcium imaging and electrophysiology has seen a dramatic increase in the size and extent of neural recordings. Even so, interpretation of this data requires considerable knowledge about the nature of the representation and often depends on manual operations. Decoding provides a means to infer the information content of such recordings but typically requires highly processed data and prior knowledge of the encoding scheme. Here, we developed a deep-learning framework able to decode sensory and behavioral variables directly from wide-band neural data. The network requires little user input and generalizes across stimuli, behaviors, brain regions, and recording techniques. Once trained, it can be analyzed to determine elements of the neural code that are informative about a given variable. We validated this approach using electrophysiological and calcium-imaging data from rodent auditory cortex and hippocampus as well as human electrocorticography (ECoG) data. We show successful decoding of finger movement, auditory stimuli, and spatial behaviors – including a novel representation of head direction - from raw neural activity.


2020 ◽  
Vol 16 (11) ◽  
pp. e1008330
Author(s):  
Marcus A. Triplett ◽  
Zac Pujic ◽  
Biao Sun ◽  
Lilach Avitan ◽  
Geoffrey J. Goodhill

The pattern of neural activity evoked by a stimulus can be substantially affected by ongoing spontaneous activity. Separating these two types of activity is particularly important for calcium imaging data given the slow temporal dynamics of calcium indicators. Here we present a statistical model that decouples stimulus-driven activity from low dimensional spontaneous activity in this case. The model identifies hidden factors giving rise to spontaneous activity while jointly estimating stimulus tuning properties that account for the confounding effects that these factors introduce. By applying our model to data from zebrafish optic tectum and mouse visual cortex, we obtain quantitative measurements of the extent that neurons in each case are driven by evoked activity, spontaneous activity, and their interaction. By not averaging away potentially important information encoded in spontaneous activity, this broadly applicable model brings new insight into population-level neural activity within single trials.


2020 ◽  
Author(s):  
Darian Hadjiabadi ◽  
Matthew Lovett-Barron ◽  
Ivan Raikov ◽  
Fraser Sparks ◽  
Zhenrui Liao ◽  
...  

AbstractNeurological and psychiatric disorders are associated with pathological neural dynamics. The fundamental connectivity patterns of cell-cell communication networks that enable pathological dynamics to emerge remain unknown. We studied epileptic circuits using a newly developed integrated computational pipeline applied to cellular resolution functional imaging data. Control and preseizure neural dynamics in larval zebrafish and in chronically epileptic mice were captured using large-scale cellular-resolution calcium imaging. Biologically constrained effective connectivity modeling extracted the underlying cell-cell communication network. Novel analysis of the higher-order network structure revealed the existence of ‘superhub’ cells that are unusually richly connected to the rest of the network through feedforward motifs. Instability in epileptic networks was causally linked to superhubs whose involvement in feedforward motifs critically enhanced downstream excitation. Disconnecting individual superhubs was significantly more effective in stabilizing epileptic networks compared to disconnecting hub cells defined traditionally by connection count. Collectively, these results predict a new, maximally selective and minimally invasive cellular target for seizure control.HighlightsHigher-order connectivity patterns of large-scale neuronal communication networks were studied in zebrafish and miceControl and epileptic networks were modeled from in vivo cellular resolution calcium imaging dataRare ‘superhub’ cells unusually richly connected to the rest of the network through higher-order feedforward motifs were identifiedDisconnecting single superhub neurons more effectively stabilized epileptic networks than targeting conventional hub cells defined by high connection count.These data predict a maximally selective novel single cell target for minimally invasive seizure control


2017 ◽  
Author(s):  
Philipp Berens ◽  
Jeremy Freeman ◽  
Thomas Deneux ◽  
Nicolay Chenkov ◽  
Thomas McColgan ◽  
...  

In recent years, two-photon calcium imaging has become a standard tool to probe the function of neural circuits and to study computations in neuronal populations. However, the acquired signal is only an indirect measurement of neural activity due to the comparatively slow dynamics of fluorescent calcium indicators. Different algorithms for estimating spike trains from noisy calcium measurements have been proposed in the past, but it is an open question how far performance can be improved. Here, we report the results of the spikefinder challenge, launched to catalyze the development of new spike inference algorithms through crowd-sourcing. We present ten of the submitted algorithms which show improved performance compared to previously evaluated methods. Interestingly, the top-performing algorithms are based on a wide range of principles from deep neural networks to generative models, yet provide highly correlated estimates of the neural activity. The competition shows that benchmark challenges can drive algorithmic developments in neuroscience.


2019 ◽  
Author(s):  
Shreya Saxena ◽  
Ian Kinsella ◽  
Simon Musall ◽  
Sharon H. Kim ◽  
Jozsef Meszaros ◽  
...  

Widefield calcium imaging enables recording of large-scale neural activity across the mouse dorsal cortex. In order to examine the relationship of these neural signals to the resulting behavior, it is critical to demix the recordings into meaningful spatial and temporal components that can be mapped onto well-defined brain regions. However, no current tools satisfactorily extract the activity of the different brain regions in individual mice in a data-driven manner, while taking into account mouse-specific and preparation-specific differences. Here, we introduce Localized semi-Nonnegative Matrix Factorization (LocaNMF), a method that efficiently decomposes widefield video data and allows us to directly compare activity across multiple mice by outputting mouse-specific localized functional regions that are significantly more interpretable than more traditional decomposition techniques. Moreover, it provides a natural subspace to directly compare correlation maps and neural dynamics across different behaviors, mice, and experimental conditions, and enables identification of task- and movement-related brain regions.


2021 ◽  
Author(s):  
Ryoma Hattori ◽  
Takaki Komiyama

Two-photon microscopy has been widely used to record the activity of populations of individual neurons at high spatial resolution in behaving animals. The ability to perform imaging for an extended period of time allows the investigation of activity changes associated with behavioral states and learning. However, imaging often accompanies shifts of the imaging field, including rapid (~100ms) translation and slow, spatially non-uniform distortion. To combat this issue and obtain a stable time series of the target structures, motion correction algorithms are commonly applied. However, typical motion correction algorithms are limited to full field translation of images and are unable to correct non-uniform distortions. Here, we developed a novel algorithm, PatchWarp, to robustly correct slow image distortion for calcium imaging data. PatchWarp is a two-step algorithm with rigid and non-rigid image registrations. To correct non-uniform image distortions, it splits the imaging field and estimates the best affine transformation matrix for each of the subfields. The distortion-corrected subfields are stitched together like a patchwork to reconstruct the distortion-corrected imaging field. We show that PatchWarp robustly corrects image distortions of calcium imaging data collected from various cortical areas through glass window or GRIN lens with a higher accuracy than existing non-rigid algorithms. Furthermore, it provides a fully automated method of registering images from different imaging sessions for longitudinal neural activity analyses. PatchWarp improves the quality of neural activity analyses and would be useful as a general approach to correct image distortions in a wide range of disciplines.


2019 ◽  
Author(s):  
Marcus A. Triplett ◽  
Zac Pujic ◽  
Biao Sun ◽  
Lilach Avitan ◽  
Geoffrey J. Goodhill

AbstractThe pattern of neural activity evoked by a stimulus can be substantially affected by ongoing spontaneous activity. Separating these two types of activity is particularly important for calcium imaging data given the slow temporal dynamics of calcium indicators. Here we present a statistical model that decouples stimulus-driven activity from low dimensional spontaneous activity in this case. The model identifies hidden factors giving rise to spontaneous activity while jointly estimating stimulus tuning properties that account for the confounding effects that these factors introduce. By applying our model to data from zebrafish optic tectum and mouse visual cortex, we obtain quantitative measurements of the extent that neurons in each case are driven by evoked activity, spontaneous activity, and their interaction. This broadly applicable model brings new insight into population-level neural activity in single trials without averaging away potentially important information encoded in spontaneous activity.


2017 ◽  
Author(s):  
Andrea Giovannucci ◽  
Johannes Friedrich ◽  
Matt Kaufman ◽  
Anne Churchland ◽  
Dmitri Chklovskii ◽  
...  

AbstractOptical imaging methods using calcium indicators are critical for monitoring the activity of large neuronal populations in vivo. Imaging experiments typically generate a large amount of data that needs to be processed to extract the activity of the imaged neuronal sources. While deriving such processing algorithms is an active area of research, most existing methods require the processing of large amounts of data at a time, rendering them vulnerable to the volume of the recorded data, and preventing realtime experimental interrogation. Here we introduce OnACID, an Online framework for the Analysis of streaming Calcium Imaging Data, including i) motion artifact correction, ii) neuronal source extraction, and iii) activity denoising and deconvolution. Our approach combines and extends previous work on online dictionary learning and calcium imaging data analysis, to deliver an automated pipeline that can discover and track the activity of hundreds of cells in real time, thereby enabling new types of closed-loop experiments. We apply our algorithm on two large scale experimental datasets, benchmark its performance on manually annotated data, and show that it outperforms a popular offline approach.


Neuron ◽  
2009 ◽  
Vol 63 (6) ◽  
pp. 747-760 ◽  
Author(s):  
Eran A. Mukamel ◽  
Axel Nimmerjahn ◽  
Mark J. Schnitzer

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