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Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study

Simple cells in primary visual cortex were famously found to respond to low-level image components such as edges. Sparse coding and independent component analysis (ICA) emerged as the standard computational models for simple cell coding because they linked their receptive fields to the statistics of...

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Autores principales: Bornschein, Jörg, Henniges, Marc, Lücke, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675001/
https://www.ncbi.nlm.nih.gov/pubmed/23754938
http://dx.doi.org/10.1371/journal.pcbi.1003062
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author Bornschein, Jörg
Henniges, Marc
Lücke, Jörg
author_facet Bornschein, Jörg
Henniges, Marc
Lücke, Jörg
author_sort Bornschein, Jörg
collection PubMed
description Simple cells in primary visual cortex were famously found to respond to low-level image components such as edges. Sparse coding and independent component analysis (ICA) emerged as the standard computational models for simple cell coding because they linked their receptive fields to the statistics of visual stimuli. However, a salient feature of image statistics, occlusions of image components, is not considered by these models. Here we ask if occlusions have an effect on the predicted shapes of simple cell receptive fields. We use a comparative approach to answer this question and investigate two models for simple cells: a standard linear model and an occlusive model. For both models we simultaneously estimate optimal receptive fields, sparsity and stimulus noise. The two models are identical except for their component superposition assumption. We find the image encoding and receptive fields predicted by the models to differ significantly. While both models predict many Gabor-like fields, the occlusive model predicts a much sparser encoding and high percentages of ‘globular’ receptive fields. This relatively new center-surround type of simple cell response is observed since reverse correlation is used in experimental studies. While high percentages of ‘globular’ fields can be obtained using specific choices of sparsity and overcompleteness in linear sparse coding, no or only low proportions are reported in the vast majority of studies on linear models (including all ICA models). Likewise, for the here investigated linear model and optimal sparsity, only low proportions of ‘globular’ fields are observed. In comparison, the occlusive model robustly infers high proportions and can match the experimentally observed high proportions of ‘globular’ fields well. Our computational study, therefore, suggests that ‘globular’ fields may be evidence for an optimal encoding of visual occlusions in primary visual cortex.
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spelling pubmed-36750012013-06-10 Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study Bornschein, Jörg Henniges, Marc Lücke, Jörg PLoS Comput Biol Research Article Simple cells in primary visual cortex were famously found to respond to low-level image components such as edges. Sparse coding and independent component analysis (ICA) emerged as the standard computational models for simple cell coding because they linked their receptive fields to the statistics of visual stimuli. However, a salient feature of image statistics, occlusions of image components, is not considered by these models. Here we ask if occlusions have an effect on the predicted shapes of simple cell receptive fields. We use a comparative approach to answer this question and investigate two models for simple cells: a standard linear model and an occlusive model. For both models we simultaneously estimate optimal receptive fields, sparsity and stimulus noise. The two models are identical except for their component superposition assumption. We find the image encoding and receptive fields predicted by the models to differ significantly. While both models predict many Gabor-like fields, the occlusive model predicts a much sparser encoding and high percentages of ‘globular’ receptive fields. This relatively new center-surround type of simple cell response is observed since reverse correlation is used in experimental studies. While high percentages of ‘globular’ fields can be obtained using specific choices of sparsity and overcompleteness in linear sparse coding, no or only low proportions are reported in the vast majority of studies on linear models (including all ICA models). Likewise, for the here investigated linear model and optimal sparsity, only low proportions of ‘globular’ fields are observed. In comparison, the occlusive model robustly infers high proportions and can match the experimentally observed high proportions of ‘globular’ fields well. Our computational study, therefore, suggests that ‘globular’ fields may be evidence for an optimal encoding of visual occlusions in primary visual cortex. Public Library of Science 2013-06-06 /pmc/articles/PMC3675001/ /pubmed/23754938 http://dx.doi.org/10.1371/journal.pcbi.1003062 Text en © 2013 Bornschein et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bornschein, Jörg
Henniges, Marc
Lücke, Jörg
Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title_full Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title_fullStr Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title_full_unstemmed Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title_short Are V1 Simple Cells Optimized for Visual Occlusions? A Comparative Study
title_sort are v1 simple cells optimized for visual occlusions? a comparative study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675001/
https://www.ncbi.nlm.nih.gov/pubmed/23754938
http://dx.doi.org/10.1371/journal.pcbi.1003062
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