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. 2022 Apr 28;13:2303. doi: 10.1038/s41467-022-29433-y

Fig. 4. Second model stage. Afferent sorting in the cortical subplate.

Fig. 4

a The model sorts afferents by retinotopy, eye input and ONOFF polarity. The sorting by eye input is done by performing a convolution between an afferent sorting filter and a binary randomized cortical subplate that assigns values of 1 to afferents from the contralateral eye (black pixels) and -1 to afferents from the ipsilateral eye (white pixels). The model selects an afferent (left, red outline) and computes the convolution at 9 neighboring positions (middle). Then, it selects the position that gives the highest convolution value (right), which is the position where the afferent is surrounded by the largest number of afferents of the same type. b Sorting of afferents by eye input in a larger cortical plate. The afferent sorting is performed in 10 developmental steps based on the convolutions with the afferent sorting filter (concentric purple and orange circles on the left). The afferents are randomly organized at step 0 (left), start segregating at step 1 (middle) and the segregation is complete at step 10 (right). c The same sorting method is used for ONOFF polarity. At the end of the sorting process, afferents are segregated by eye input and ONOFF polarity (left) in addition to retinotopy (right). d Random afferent sorting by retinotopy causes random mapping of all stimulus dimensions in simulated visual cortex. From left to right, mapping of retinotopy, ocular dominance, ONOFF polarity and orientation preference for the contralateral eye. e Random afferent sorting by eye input causes random mapping of all stimulus dimensions except retinotopy in simulated cortex. From left to right, normal cortical retinotopy and random mapping for ocular dominance, ONOFF polarity and orientation preference. f Random afferent sorting for ONOFF polarity causes random cortical mapping of all stimulus dimensions except retinotopy and eye input. From left to right, pairs of panels showing cortical retinotopy for both eyes, afferent segregation by eye input but not ONOFF polarity, and random mapping of orientation preference and selectivity for both eyes.