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Beyond l1 sparse coding in V1

delete2023-09-12
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I
Ilias Rentzeperis *
L
Luca Calatroni
L
Laurent Perrinet
D
Dario Prandi
DOI:10.1371/journal.pcbi.1011459delete
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Abstract

Abstract

En 中文
Growing evidence indicates that only a sparse subset from a pool of sensory neurons is active for the encoding of visual stimuli at any instant in time. Traditionally, to replicate such biological sparsity, generative models have been using the l1 norm as a penalty due to its convexity, which makes it amenable to fast and simple algorithmic solvers. In this work, we use biological vision as a test-bed and show that the soft thresholding operation associated to the use of the l1 norm is highly suboptimal compared to other functions suited to approximating lp with 0 = p < 1 (including recently proposed continuous exact relaxations), in terms of performance. We show that l1 sparsity employs a pool with more neurons, i.e. has a higher degree of overcompleteness, in order to maintain the same reconstruction error as the other methods considered. More specifically, at the same sparsity level, the thresholding algorithm using the l1 norm as a penalty requires a dictionary of ten times more units compared to the proposed approach, where a non-convex continuous relaxation of the l0 pseudo-norm is used, to reconstruct the external stimulus equally well. At a fixed sparsity level, both l0- and l1-based regularization develop units with receptive field (RF) shapes similar to biological neurons in V1 (and a subset of neurons in V2), but l0-based regularization shows approximately five times better reconstruction of the stimulus. Our results in conjunction with recent metabolic findings indicate that for V1 to operate efficiently it should follow a coding regime which uses a regularization that is closer to the l0 pseudo-norm rather than the l1 one, and suggests a similar mode of operation for the sensory cortex in general.
Keywords:
VISUAL-CORTEX
MACAQUE V1
ORIENTATION SELECTIVITY
L-1/2 REGULARIZATION
SPATIAL STRUCTURE
RECEPTIVE-FIELDS
REPRESENTATION
SEGREGATION
ALGORITHM
NETWORK
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PLOS Biology cover
PLOS Biology
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Universite Paris Saclay
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