Ontology highlight
ABSTRACT: Objective
Although optical imaging of neurons using fluorescent genetically encoded calcium sensors has enabled large-scale in vivo experiments, the sensors' slow dynamics often blur closely timed action potentials into indistinguishable transients. While several previous approaches have been proposed to estimate the timing of individual spikes, they have overlooked the important and practical problem of estimating interspike interval (ISI) for overlapping transients.Methods
We use statistical detection theory to find the minimum detectable ISI under different levels of signal-to-noise ratio (SNR), model complexity, and recording speed. We also derive the Cramer-Rao lower bounds (CRBs) for the problem of ISI estimation. We use Monte-Carlo simulations with biologically derived parameters to numerically obtain the minimum detectable ISI and evaluate the performance of our estimators. Furthermore, we apply our detector to distinguish overlapping transients from experimentally obtained calcium imaging data.Results
Experiments based on simulated and real data across different SNR levels and recording speeds show that our algorithms can accurately distinguish two fluorescence signals with ISI on the order of tens of milliseconds, shorter than the waveform's rise time. Our study shows that the statistically optimal ISI estimators closely approached the CRBs.Conclusion
Our work suggests that full analysis using recording speed, sensor kinetics, SNR, and the sensor's stochastically distributed response to action potentials can accurately resolve ISIs much smaller than the fluorescence waveform's rise time in modern calcium imaging experiments.Significance
Such analysis aids not only in future spike detection methods, but also in future experimental design when choosing sensors of neuronal activity.
SUBMITTER: Soltanian-Zadeh S
PROVIDER: S-EPMC6230443 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature
IEEE transactions on bio-medical engineering 20180308 11
<h4>Objective</h4>Although optical imaging of neurons using fluorescent genetically encoded calcium sensors has enabled large-scale in vivo experiments, the sensors' slow dynamics often blur closely timed action potentials into indistinguishable transients. While several previous approaches have been proposed to estimate the timing of individual spikes, they have overlooked the important and practical problem of estimating interspike interval (ISI) for overlapping transients.<h4>Methods</h4>We u ...[more]