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. 2017 Dec 6;8:1964. doi: 10.1038/s41467-017-02159-y

Fig. 3.

Fig. 3

Responses of ON ganglion cells to the randomly moving bar. a Schematic of the LN model, composed of a linear filter and static nonlinearity. Filled arrows correspond to learned weights of the model. b Response (PSTH, black) of a ganglion cell whose receptive field center is stimulated by the bar, is not well predicted by the LN model (blue). r = 0.56. c Response (PSTH, black) of the same ganglion cell when the bar is far from the receptive field center, is not predicted well by the LN model (blue). r = 0.01. d Schematic of the subunit model, composed of a first stage (each subunit linearly filters the stimulus and applies a static nonlinearity), followed by weighted linear pooling and a second nonlinearity (see Methods section for details). Filled arrows correspond to learned weights of the model. e Response (PSTH, black) of the same ganglion cell (as in b, c) to central stimulation is predicted well by the subunit model (red). r = 0.9. f Response (PSTH, black) of the same ganglion cell (as in b, c) to distant stimulation is predicted well by the subunit model (red). r = 0.77. g Receptive fields of a population of ON ganglion cells of the same type. Each ellipse represents the position and shape of the spatial receptive field associated with one cell (1-SD contour of the 2D Gaussian fit to the spatial profile of the RF). Inset: temporal profiles of the receptive fields of the same cells. h Performance of the LN (blue) and subunit (red) models in predicting ganglion cell responses, as a function of the distance of the cell to the bar. Blue shade: position distribution of the bar