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      Inferring Nonlinear Neuronal Computation Based on Physiologically Plausible Inputs

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      PLoS Computational Biology
      Public Library of Science

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          Abstract

          The computation represented by a sensory neuron's response to stimuli is constructed from an array of physiological processes both belonging to that neuron and inherited from its inputs. Although many of these physiological processes are known to be nonlinear, linear approximations are commonly used to describe the stimulus selectivity of sensory neurons (i.e., linear receptive fields). Here we present an approach for modeling sensory processing, termed the Nonlinear Input Model (NIM), which is based on the hypothesis that the dominant nonlinearities imposed by physiological mechanisms arise from rectification of a neuron's inputs. Incorporating such ‘upstream nonlinearities’ within the standard linear-nonlinear (LN) cascade modeling structure implicitly allows for the identification of multiple stimulus features driving a neuron's response, which become directly interpretable as either excitatory or inhibitory. Because its form is analogous to an integrate-and-fire neuron receiving excitatory and inhibitory inputs, model fitting can be guided by prior knowledge about the inputs to a given neuron, and elements of the resulting model can often result in specific physiological predictions. Furthermore, by providing an explicit probabilistic model with a relatively simple nonlinear structure, its parameters can be efficiently optimized and appropriately regularized. Parameter estimation is robust and efficient even with large numbers of model components and in the context of high-dimensional stimuli with complex statistical structure (e.g. natural stimuli). We describe detailed methods for estimating the model parameters, and illustrate the advantages of the NIM using a range of example sensory neurons in the visual and auditory systems. We thus present a modeling framework that can capture a broad range of nonlinear response functions while providing physiologically interpretable descriptions of neural computation.

          Author Summary

          Sensory neurons are capable of representing a wide array of computations on sensory stimuli. Such complex computations are thought to arise in large part from the accumulation of relatively simple nonlinear operations across the sensory processing hierarchies. However, models of sensory processing typically rely on mathematical approximations of the overall relationship between stimulus and response, such as linear or quadratic expansions, which can overlook critical elements of sensory computation and miss opportunities to reveal how the underlying inputs contribute to a neuron's response. Here we present a physiologically inspired nonlinear modeling framework, the ‘Nonlinear Input Model’ (NIM), which instead assumes that neuronal computation can be approximated as a sum of excitatory and suppressive ‘neuronal inputs’. We show that this structure is successful at explaining neuronal responses in a variety of sensory areas. Furthermore, model fitting can be guided by prior knowledge about the inputs to a given neuron, and its results can often suggest specific physiological predictions. We illustrate the advantages of the proposed model and demonstrate specific parameter estimation procedures using a range of example sensory neurons in both the visual and auditory systems.

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          Spatio-temporal correlations and visual signalling in a complete neuronal population.

          Statistical dependencies in the responses of sensory neurons govern both the amount of stimulus information conveyed and the means by which downstream neurons can extract it. Although a variety of measurements indicate the existence of such dependencies, their origin and importance for neural coding are poorly understood. Here we analyse the functional significance of correlated firing in a complete population of macaque parasol retinal ganglion cells using a model of multi-neuron spike responses. The model, with parameters fit directly to physiological data, simultaneously captures both the stimulus dependence and detailed spatio-temporal correlations in population responses, and provides two insights into the structure of the neural code. First, neural encoding at the population level is less noisy than one would expect from the variability of individual neurons: spike times are more precise, and can be predicted more accurately when the spiking of neighbouring neurons is taken into account. Second, correlations provide additional sensory information: optimal, model-based decoding that exploits the response correlation structure extracts 20% more information about the visual scene than decoding under the assumption of independence, and preserves 40% more visual information than optimal linear decoding. This model-based approach reveals the role of correlated activity in the retinal coding of visual stimuli, and provides a general framework for understanding the importance of correlated activity in populations of neurons.
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            A point process framework for relating neural spiking activity to spiking history, neural ensemble, and extrinsic covariate effects.

            Multiple factors simultaneously affect the spiking activity of individual neurons. Determining the effects and relative importance of these factors is a challenging problem in neurophysiology. We propose a statistical framework based on the point process likelihood function to relate a neuron's spiking probability to three typical covariates: the neuron's own spiking history, concurrent ensemble activity, and extrinsic covariates such as stimuli or behavior. The framework uses parametric models of the conditional intensity function to define a neuron's spiking probability in terms of the covariates. The discrete time likelihood function for point processes is used to carry out model fitting and model analysis. We show that, by modeling the logarithm of the conditional intensity function as a linear combination of functions of the covariates, the discrete time point process likelihood function is readily analyzed in the generalized linear model (GLM) framework. We illustrate our approach for both GLM and non-GLM likelihood functions using simulated data and multivariate single-unit activity data simultaneously recorded from the motor cortex of a monkey performing a visuomotor pursuit-tracking task. The point process framework provides a flexible, computationally efficient approach for maximum likelihood estimation, goodness-of-fit assessment, residual analysis, model selection, and neural decoding. The framework thus allows for the formulation and analysis of point process models of neural spiking activity that readily capture the simultaneous effects of multiple covariates and enables the assessment of their relative importance.
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              A simple white noise analysis of neuronal light responses.

              A white noise technique is presented for estimating the response properties of spiking visual system neurons. The technique is simple, robust, efficient and well suited to simultaneous recordings from multiple neurons. It provides a complete and easily interpretable model of light responses even for neurons that display a common form of response nonlinearity that precludes classical linear systems analysis. A theoretical justification of the technique is presented that relies only on elementary linear algebra and statistics. Implementation is described with examples. The technique and the underlying model of neural responses are validated using recordings from retinal ganglion cells, and in principle are applicable to other neurons. Advantages and disadvantages of the technique relative to classical approaches are discussed.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput. Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, USA )
                1553-734X
                1553-7358
                July 2013
                July 2013
                18 July 2013
                : 9
                : 7
                : e1003143
                Affiliations
                [1]Department of Biology and Program in Neuroscience and Cognitive Science, University of Maryland, College Park, Maryland, United States of America
                University of Tübingen and Max Planck Institute for Biologial Cybernetics, Germany
                Author notes

                The authors have declared that no competing interests exist.

                Analyzed the data: JMM YC DAB. Wrote the paper: JMM DAB. Developed the model: JMM YC DAB.

                Article
                PCOMPBIOL-D-12-01586
                10.1371/journal.pcbi.1003143
                3715434
                23874185
                79a0f986-f8e8-4607-b1f0-f68057e8be51
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 3 October 2012
                : 1 June 2013
                Page count
                Pages: 18
                Funding
                All authors were supported by NSF IIS-0904430 ( www.nsf.gov). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Neuroscience
                Computational Neuroscience
                Sensory Systems
                Single Neuron Function
                Sensory Systems
                Auditory System
                Visual System
                Mathematics
                Statistics
                Statistical Methods

                Quantitative & Systems biology
                Quantitative & Systems biology

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