Modeling the impact of common noise inputs on the network activity
of retinal ganglion cells
Vidne M, Ahmadian Y, Shlens J, Pillow JW, Kulkarni J, Litke AM, Chichilnisky EJ, Simoncelli EP, & Paninski L.
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J Comput Neurosci, 1-25 (2012). to appear
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Synchronized spontaneous firing among retinal ganglion cells
(RGCs), on timescales faster than visual responses, has been reported
in many studies. Two candidate mechanisms of synchronized firing
include direct coupling and shared noisy inputs. In neighboring
parasol cells of primate retina, which exhibit rapid synchronized
firing that has been studied extensively, recent experimental work
indicates that direct electrical or synaptic coupling is weak, but
shared synaptic input in the absence of modulated stimuli is
strong. However, previous modeling efforts have not accounted for this
aspect of firing in the parasol cell population. Here we develop a new
model that incorporates the effects of common noise, and apply it to
analyze the light responses and synchronized firing of a large,
densely- sampled network of over 250 simultaneously recorded parasol
cells. We use a generalized linear model in which the spike rate in
each cell is determined by the linear combination of the
spatio-temporally filtered visual input, the temporally filtered prior
spikes of that cell, and unobserved sources representing common
noise. The model accurately captures the statistical structure of the
spike trains and the encoding of the visual stimulus, without the
direct coupling assump- tion present in previous modeling
work. Finally, we examined the problem of decoding the visual stimulus
from the spike train given the estimated parameters. The common-noise
model produces Bayesian decod- ing performance as accurate as that of
a model with direct coupling, but with significantly more robustness
to spike timing perturbations.
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