Neural anatomy and optical microscopy (NAOMi) simulation for evaluating calcium imaging methods
| Autor: | David W. Tank, Adam S. Charles, Jeffrey L. Gauthier, Alexander Song, Jonathan W. Pillow |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
0301 basic medicine
Computer science Gaussian ComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISION Article law.invention symbols.namesake 03 medical and health sciences Mice 0302 clinical medicine Optical microscope Two-photon excitation microscopy law Microscopy Leverage (statistics) Animals Segmentation Computer Simulation Spatial analysis 030304 developmental biology 0303 health sciences Ground truth Mouse cortex General Neuroscience Optical physics Anatomy Numerical aperture Functional imaging 030104 developmental biology symbols Calcium Artifacts 030217 neurology & neurosurgery Algorithms |
| Zdroj: | J Neurosci Methods |
| ISSN: | 1872-678X |
| Popis: | Background The past decade has seen a multitude of new in vivo functional imaging methodologies. However, the lack of ground-truth comparisons or evaluation metrics makes the large-scale, systematic validation vital to the continued development and use of optical microscopy impossible. New-method We provide a new framework for evaluating two-photon microscopy methods via in silico Neural Anatomy and Optical Microscopy (NAOMi) simulation. Our computationally efficient model generates large anatomical volumes of mouse cortex, simulates neural activity, and incorporates optical propagation and scanning to create realistic calcium imaging datasets. Results We verify NAOMi simulations against in vivo two-photon recordings from mouse cortex. We leverage this in silico ground truth to directly compare different segmentation algorithms and optical designs. We find modern segmentation algorithms extract strong neural time-courses comparable to estimation using oracle spatial information, but with an increase in the false positive rate. Comparison between optical setups demonstrate improved resilience to motion artifacts in sparsely labeled samples using Bessel beams, increased signal-to-noise ratio and cell-count using low numerical aperture Gaussian beams and nuclear GCaMP, and more uniform spatial sampling with temporal focusing versus multi-plane imaging. Comparison with existing methods NAOMi is a first-of-its kind framework for assessing optical imaging modalities. Existing methods are either anatomical simulations or do not address functional imaging. Thus there is no competing method for simulating realistic functional optical microscopy data. Conclusions By leveraging the rich accumulated knowledge of neural anatomy and optical physics, we provide a powerful new tool to assess and develop important methods in neural imaging. |
| Databáze: | OpenAIRE |
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