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Illustration of: (a) neuron, (b) action potential, and (c) spike activity s with different stimulus levels and resulting calcium concentration c.

Illustration of: (a) neuron, (b) action potential, and (c) spike activity s with different stimulus levels and resulting calcium concentration c.

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Extracting and detecting spike activities from the fluorescence observations is an important step in understanding how neuron systems work. The main challenge lies in the combined ambient noise with fluctuated baseline, which contaminates the observations, thereby deteriorating the reliability of spike detection. This may be even worse in the face...

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... data (e.g., the brain science, the cell communications, and sequencing [5], [6]), as the changes of calcium-ion concentration reflect the occurrence of most cell functions [7]. For example, in order to study the dynamic behaviors of neuron cells, neuron action potentials (spike activities) are required to be detected. As is shown in Fig. 1(a)-(b), such spike activity links to a calcium influx that may lead to a steep increase of the intracellular free calciumion. As such, detecting the neuron spike activities requires the track of the calcium concentration, which serves as the key to characterizing the neuron dynamics, and further understanding how neuron systems react ...
Context 2
... in real biological systems may guide the designs of synthetic neural systems that mimic neuron [8]- [10] and cell signaling [11]- [13]. In the context of neural activity inference, spikes, dynamical baseline, and critical model parameters are detected and estimated through the fluorescence observations from a calcium image. As is shown in Fig. 1(c), such inference is limited by three difficulties. Firstly, spikes lead to a rapid rise in intracellular calcium (Ca 2+ ) concentration followed by a slow decay (i.e., time-to-peak 8-40ms, and decay constant 0.3-1.5s [14]- [17]). This effect gives rise to the transients induced by individual spikes to overlap, and aggregating in a ...

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