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Spike Estimation From Fluorescence Signals Using High-Resolution Property of Group Delay

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TLDR
The proposed approach, GD spike, is compared with other spike estimation methods, including MLspike, Vogelstein de-convolution algorithm, and data-driven spike-triggered mixture model and shows superior results.
Abstract
Spike estimation from calcium (Ca $^{2+}$ ) fluorescence signals is a fundamental and challenging problem in neuroscience. Several models and algorithms have been proposed for this task over the past decade. Nevertheless, it is still hard to achieve accurate spike positions from the Ca $^{2+}$ fluorescence signals. While existing methods rely on data-driven methods and the physiology of neurons for modeling the spiking process, this paper exploits the nature of the fluorescence responses to spikes using signal processing. We first motivate the problem by a novel analysis of the high-resolution property of minimum-phase group delay (GD) functions for multi-pole resonators. The resonators could be connected either in series or in parallel. The Ca $^{2+}$ indicator responds to a spike with a sudden rise, that is followed by an exponential decay. We interpret the Ca $^{2+}$ signal as the response of an impulse train to the change in Ca $^{2+}$ concentration, where the Ca $^{2+}$ response corresponds to a resonator. We perform minimum-phase GD-based filtering of the Ca $^{2+}$ signal for resolving spike locations. The performance of the proposed algorithm is evaluated on nine datasets spanning various indicators, sampling rates, and mouse brain regions. The proposed approach, GDspike, is compared with other spike estimation methods, including MLspike, Vogelstein de-convolution algorithm, and data-driven spike-triggered mixture model. The performance of GDspike is superior to that of the Vogelstein algorithm and is comparable to that of MLspike. It can also be used to post-process the output of MLspike, which further enhances the performance.

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Journal ArticleDOI

Reliable Sensory Processing in Mouse Visual Cortex through Cooperative Interactions between Somatostatin and Parvalbumin Interneurons

TL;DR: In this paper, the role of different inhibitory interneurons (INs) in reliable coding in the primary visual cortex (V1) was investigated. But, the same neurons can also respond highly reliably.
Journal ArticleDOI

Signal-to-signal neural networks for improved spike estimation from calcium imaging data

TL;DR: In this paper, a neural network-based signal-to-signal conversion approach is proposed to estimate the spike information in an end-toend fashion, where the source corresponding to the action potentials at a lower resolution is estimated at the output.
Posted ContentDOI

Signal-to-signal networks for improved spike estimation from calcium imaging data

TL;DR: A novel neural network-based data-driven algorithm that takes the fluorescence recording as the input and synthesizes the spike information signal, which is well-correlated with the actual spike positions, and outperforms state-of-the-art methods on standard evaluation framework.
Journal ArticleDOI

Importance of Signal Processing Cues in Transcription Correction for Low-Resource Indian Languages

TL;DR: The issue of vowel deletions is studied and group-delay-based segmentation is used to determine insertion/deletion of vowels in the speech utterance and the transcriptions are corrected in the training data based on this.
Posted ContentDOI

High frequency spike inference with particle Gibbs sampling

TL;DR: This study introduces an auto-regressive generative model that accounts for bursting neuronal activity and baseline fluorescence modulation, and it also applies recent sequential Monte Carlo approaches to obtain joint posterior distributions of static and dynamic model parameters.
References
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TL;DR: A family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice in vivo are developed and provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
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In vivo two-photon calcium imaging of neuronal networks

TL;DR: In vivo two-photon calcium imaging recordings indicated that whisker deflection-evoked Ca2+ transients occur in a subset of layer 2/3 neurons of the barrel cortex, demonstrating the suitability of this technique for real-time analyses of intact neuronal circuits with the resolution of individual cells.
Journal ArticleDOI

Simultaneous Denoising, Deconvolution, and Demixing of Calcium Imaging Data

TL;DR: This work presents a modular approach for analyzing calcium imaging recordings of large neuronal ensembles that 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 neurons in the optical field and a temporal matrix that characterizes the calcium concentration of each neuron over time.
Journal ArticleDOI

Sensitive red protein calcium indicators for imaging neural activity

TL;DR: Improved red GECIs based on mRuby (jRCaMP1a, b) and mApple (jRGECO1a) are presented, with sensitivity comparable to GCaMP6, to facilitate deep-tissue imaging, dual-color imaging together with GFP-based reporters, and the use of optogenetics in combination with calcium imaging.
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