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Spectral methods for neural characterization using generalized quadratic models

机译:使用广义二次模型的神经表征光谱方法

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We describe a set of fast, tractable methods for characterizing neural responses to high-dimensional sensory stimuli using a model we refer to as the generalized quadratic model (GQM). The GQM consists of a low-rank quadratic function followed by a point nonlinearity and exponential-family noise. The quadratic function characterizes the neuron's stimulus selectivity in terms of a set linear receptive fields followed by a quadratic combination rule, and the invertible nonlinearity maps this output to the desired response range. Special cases of the GQM include the 2nd-order Volterra model and the elliptical Linear-Nonlinear-Poisson model. Here we show that for "canonical form" GQMs, spectral decomposition of the first two response-weighted moments yields approximate maximum-likelihood estimators via a quantity called the expected log-likelihood. The resulting theory generalizes moment-based estimators such as the spike-triggered co-variance, and, in the Gaussian noise case, provides closed-form estimators under a large class of non-Gaussian stimulus distributions. We show that these estimators are fast and provide highly accurate estimates with far lower computational cost than full maximum likelihood. Moreover, the GQM provides a natural framework for combining multi-dimensional stimulus sensitivity and spike-history dependencies within a single model. We show applications to both analog and spiking data using intracellular recordings of V1 membrane potential and extracellular recordings of retinal spike trains.
机译:我们描述了一系列快速,易易易读的方法,用于使用我们称为广义二次模型(GQM)的模型来表征对高维感官刺激的神经响应。 GQM由低秩二次函数组成,然后是点非线性和指数家庭噪声。二次函数表征了内核的刺激选择性,即在设置线性接收领域,然后是二次组合规则,并且可逆的非线性将该输出映射到所需的响应范围。 GQM的特殊情况包括2nd阶Volterra模型和椭圆线性非线性 - 泊松模型。在这里,我们表明,对于“规范形式”GQM,前两个响应加权时刻的光谱分解通过称为预期的对数似然的数量产生近似的最大似然估计。由此产生的理论概括了诸如Spike触发的共方的矩的估计器,并且在高斯噪声壳体中,在大类非高斯刺激分布下提供闭合型估计。我们表明这些估计器快速,提供了高度准确的估计,其计算成本远低于完全最大可能性。此外,GQM提供了一种自然框架,用于将多维刺激灵敏度和峰值历史依赖性组合在单个模型中。我们将应用于模拟和尖峰数据使用V1膜势的细胞内记录和视网膜尖峰列车的细胞外记录。

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