Skip to main content
. Author manuscript; available in PMC: 2023 Aug 3.
Published in final edited form as: Neuron. 2022 Jun 8;110(15):2484–2502.e16. doi: 10.1016/j.neuron.2022.05.012

Figure 8. High dimensional representation of conjunctive variables across posterior cortex.

Figure 8.

(A) Fraction explained deviance of cue for the top 25% cue-selective neurons across all cells, separated in 6 areas and sorted by peak location.

(B) Same as (A), except the top 25% of dynamic choice-selective neurons.

(C) Left: average decoding performance for cue based on populations of ~100 nearby neurons for 6 areas, quantified as log likelihood with log base 2. Right: change in decoding performance as a function of the distance between maze positions of the data that the decoders were trained on and tested on (restricted to positions where cue was present). n = 698 decoders.

(D) Same as (C), but for decoding performance of dynamic choice, quantified as the Spearman correlation between decoded and real values. n = 974 decoders.

(E) Schematic for identifying marginally balanced dichotomies over conjunctive conditions formed by a pair of variables.

(F) Spatial maps of shattering dimensionality (average decoding accuracy over all marginally balanced dichotomies) during stem traversal. Each dot indicates a population of 1000 nearby neurons centered on that cortical location.

(G) Shattering dimensionality based on populations of 1000 neurons subsampled from all neurons and each of the 6 areas. All datapoints were not significantly different from one another (p > 0.01, not significant after multiple comparison correction).

Data and statistics in (C), (D), (G) are presented as hierarchical bootstrap mean ± SEM.

See also Figure S8.