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The Population Tracking Model: A Simple, Scalable Statistical Model for Neural Population Data

机译:人口跟踪模型:神经人口数据的简单,可扩展的统计模型

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摘要

Our understanding of neural population coding has been limited by a lack of analysis methods to characterize spiking data from large populations. The biggest challenge comes from the fact that the number of possible network activity patterns scales exponentially with the number of neurons recorded (). Here we introduce a new statistical method for characterizing neural population activity that requires semi-independent fitting of only as many parameters as the square of the number of neurons, requiring drastically smaller data sets and minimal computation time. The model works by matching the population rate (the number of neurons synchronously active) and the probability that each individual neuron fires given the population rate. We found that this model can accurately fit synthetic data from up to 1000 neurons. We also found that the model could rapidly decode visual stimuli from neural population data from macaque primary visual cortex about 65 ms after stimulus onset. Finally, we used the model to estimate the entropy of neural population activity in developing mouse somatosensory cortex and, surprisingly, found that it first increases, and then decreases during development. This statistical model opens new options for interrogating neural population data and can bolster the use of modern large-scale in vivo Ca and voltage imaging tools.
机译:我们对神经种群编码的理解受到缺乏用于表征来自大种群的峰值数据的分析方法的限制。最大的挑战来自以下事实:可能的网络活动模式的数量与记录的神经元的数量成指数比例增长。在这里,我们介绍了一种用于表征神经种群活动的新统计方法,该方法只需要半独立拟合神经元数量平方的参数,就需要非常小的数据集和最少的计算时间。该模型通过匹配种群率(同步活跃的神经元数量)和给定种群率下每个单个神经元激发的概率进行匹配。我们发现该模型可以准确地拟合多达1000个神经元的合成数据。我们还发现,该模型可以在刺激发生后约65毫秒内从猕猴初级视觉皮层的神经种群数据快速解码视觉刺激。最后,我们使用该模型估算了发育中的小鼠体感皮层中神经种群活动的熵,令人惊讶的是,发现它在发育过程中先增加,然后减少。该统计模型为询问神经种群数据开辟了新的选择,并可以支持现代大规模体内Ca和电压成像工具的使用。

著录项

  • 来源
    《Neural computation》 |2017年第1期|50-93|共44页
  • 作者单位

    Department of Computer Science, University of Bristol, Bristol BS81UB. U.K., and Howard Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, CA 92037, U.S.A. cian.odonnell@bristol.ac.uk;

    Salk Institute for Biological Studies, La Jolla, CA 92037, U.S.A., and Departments of Neurology and Neurobiology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, U.S.A. tgoncalves@salk.edu;

    School of Mathematics, University of Bristol, Bristol BS81UB, U.K. Nick.Whiteley@bristol.ac.uk;

    Departments of Neurology and Neurobiology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, U.S.A. CPCailliau@mednet.ucla.edu;

    Howard Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, CA 92037, U.S.A., and Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093, U.S.A. terry@salk.edu;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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