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Skyler Thomas

Publications and source records attributed to Skyler Thomas.

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Partitioning Neural Co-Variability

Trial-to-trial variability of neural responses has been linked to important aspects of neural computation and is essential for understanding how neuronal populations respond. While current overdispersion models treat each neuron's gain as independent of each other, this assumption fails to capture the network statistics of neuronal populations. As no existing model can capture overdispersed structured spiking gain-modulation across a neural population, network-level gain covariance remains largely unstudied. We thus present the Poisson matrix-normal latent variable (PMNLV) model, which extends single-neuron overdispersion to neural populations by placing a matrix-normal prior over the latent gain with a Kronecker-factored covariance. Spike counts are Poisson-distributed with a rate equal to the sum of a per-neuron stimulus tuning term and a matrix-normal gain, passed through a quadratic soft-rectifying link. We derive two complementary estimation algorithms: a variational EM (VEM) with a matrix-normal posterior that recovers dense Kronecker factors without structural assumptions, and a Kernel Tournament Method (KTM) that performs data-driven selection over a biologically motivated kernel dictionary and composite likelihood. On simulated data, both algorithms recover the inter-neuron and temporal covariance factors and accurate tuning curves. Applying VEM to Neuropixel recordings across four cortical regions of mouse visual hierarchy, we replicate a previous finding that single-neuron marginal variability changes little across cortical areas. We then show that shared population co-variability, invisible to scalar summaries e.g., the Fano factor, peaks in primary visual cortex and declines in higher visual areas. The PMNLV framework is applicable to any simultaneously recorded population where structured gain covariance is of scientific interest.

q-bio.QM

Fast Two-photon Microscopy by Neuroimaging with Oblong Random Acquisition (NORA)

Advances in neural imaging have enabled neuroscientists to study how large neural populations conspire to produce perception, behavior and cognition. Despite many advances in optical methods, there exists a fundamental tradeoff between imaging speed, field of view, and resolution that limits the scope of neural imaging, especially for the raster-scanning multi-photon imaging needed to image deeper into the brain. One approach to overcoming this trade-off is computational imaging: the co-development of optics designed to encode the target images into fewer measurements that are faster to acquire, with algorithms that compensate by inverting the optical coding to recover a larger or higher resolution image. We present here one such approach for raster-scanning two-photon imaging: Neuroimaging with Oblong Random Acquisition (NORA). NORA quickly acquires each frame in a microscopy video by subsampling only a fraction of the fast scanning lines, ignoring large portions of each frame. NORA mitigates the loss of information by 1) extending the point-spread function in the slow-scan direction to effectively integrate the fluorescence of several lines into a single set of measurements and 2) imaging different, randomly selected, lines at each frame. Rather than reconstruct the video frame-by-frame, NORA recovers full video sequences via nuclear-norm minimization on the pixels-by-time matrix, for which we prove theoretical guarantees on recovery. We simulated NORA imaging using the Neural Anatomy and Optical Microscopy (NAOMi) biophysical simulator, and used the simulations to demonstrate that NORA can accurately recover 400 um X 400 um fields of view at subsampling rates up to 20X, despite realistic noise and motion conditions. As NORA requires minimal changes to current microscopy systems, our results indicate that NORA can provide a promising avenue towards fast imaging of neural circuits.

eess.IV