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Decoding of human identity by computer vision and neuronal vision

Extracting meaning from a dynamic and variable flow of incoming information is a major goal of both natural and artificial intelligence. Computer vision (CV) guided by deep learning (DL) has made significant strides in recognizing a specific identity despite highly variable attributes. This is the s...

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Autores principales: Zhang, Yipeng, Aghajan, Zahra M., Ison, Matias, Lu, Qiujing, Tang, Hanlin, Kalender, Guldamla, Monsoor, Tonmoy, Zheng, Jie, Kreiman, Gabriel, Roychowdhury, Vwani, Fried, Itzhak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837190/
https://www.ncbi.nlm.nih.gov/pubmed/36635322
http://dx.doi.org/10.1038/s41598-022-26946-w
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author Zhang, Yipeng
Aghajan, Zahra M.
Ison, Matias
Lu, Qiujing
Tang, Hanlin
Kalender, Guldamla
Monsoor, Tonmoy
Zheng, Jie
Kreiman, Gabriel
Roychowdhury, Vwani
Fried, Itzhak
author_facet Zhang, Yipeng
Aghajan, Zahra M.
Ison, Matias
Lu, Qiujing
Tang, Hanlin
Kalender, Guldamla
Monsoor, Tonmoy
Zheng, Jie
Kreiman, Gabriel
Roychowdhury, Vwani
Fried, Itzhak
author_sort Zhang, Yipeng
collection PubMed
description Extracting meaning from a dynamic and variable flow of incoming information is a major goal of both natural and artificial intelligence. Computer vision (CV) guided by deep learning (DL) has made significant strides in recognizing a specific identity despite highly variable attributes. This is the same challenge faced by the nervous system and partially addressed by the concept cells—neurons exhibiting selective firing in response to specific persons/places, described in the human medial temporal lobe (MTL) ⁠. Yet, access to neurons representing a particular concept is limited due to these neurons’ sparse coding. It is conceivable, however, that the information required for such decoding is present in relatively small neuronal populations. To evaluate how well neuronal populations encode identity information in natural settings, we recorded neuronal activity from multiple brain regions of nine neurosurgical epilepsy patients implanted with depth electrodes, while the subjects watched an episode of the TV series “24”. First, we devised a minimally supervised CV algorithm (with comparable performance against manually-labeled data) to detect the most prevalent characters (above 1% overall appearance) in each frame. Next, we implemented DL models that used the time-varying population neural data as inputs and decoded the visual presence of the four main characters throughout the episode. This methodology allowed us to compare “computer vision” with “neuronal vision”—footprints associated with each character present in the activity of a subset of neurons—and identify the brain regions that contributed to this decoding process. We then tested the DL models during a recognition memory task following movie viewing where subjects were asked to recognize clip segments from the presented episode. DL model activations were not only modulated by the presence of the corresponding characters but also by participants’ subjective memory of whether they had seen the clip segment, and by the associative strengths of the characters in the narrative plot. The described approach can offer novel ways to probe the representation of concepts in time-evolving dynamic behavioral tasks. Further, the results suggest that the information required to robustly decode concepts is present in the population activity of only tens of neurons even in brain regions beyond MTL.
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spelling pubmed-98371902023-01-14 Decoding of human identity by computer vision and neuronal vision Zhang, Yipeng Aghajan, Zahra M. Ison, Matias Lu, Qiujing Tang, Hanlin Kalender, Guldamla Monsoor, Tonmoy Zheng, Jie Kreiman, Gabriel Roychowdhury, Vwani Fried, Itzhak Sci Rep Article Extracting meaning from a dynamic and variable flow of incoming information is a major goal of both natural and artificial intelligence. Computer vision (CV) guided by deep learning (DL) has made significant strides in recognizing a specific identity despite highly variable attributes. This is the same challenge faced by the nervous system and partially addressed by the concept cells—neurons exhibiting selective firing in response to specific persons/places, described in the human medial temporal lobe (MTL) ⁠. Yet, access to neurons representing a particular concept is limited due to these neurons’ sparse coding. It is conceivable, however, that the information required for such decoding is present in relatively small neuronal populations. To evaluate how well neuronal populations encode identity information in natural settings, we recorded neuronal activity from multiple brain regions of nine neurosurgical epilepsy patients implanted with depth electrodes, while the subjects watched an episode of the TV series “24”. First, we devised a minimally supervised CV algorithm (with comparable performance against manually-labeled data) to detect the most prevalent characters (above 1% overall appearance) in each frame. Next, we implemented DL models that used the time-varying population neural data as inputs and decoded the visual presence of the four main characters throughout the episode. This methodology allowed us to compare “computer vision” with “neuronal vision”—footprints associated with each character present in the activity of a subset of neurons—and identify the brain regions that contributed to this decoding process. We then tested the DL models during a recognition memory task following movie viewing where subjects were asked to recognize clip segments from the presented episode. DL model activations were not only modulated by the presence of the corresponding characters but also by participants’ subjective memory of whether they had seen the clip segment, and by the associative strengths of the characters in the narrative plot. The described approach can offer novel ways to probe the representation of concepts in time-evolving dynamic behavioral tasks. Further, the results suggest that the information required to robustly decode concepts is present in the population activity of only tens of neurons even in brain regions beyond MTL. Nature Publishing Group UK 2023-01-12 /pmc/articles/PMC9837190/ /pubmed/36635322 http://dx.doi.org/10.1038/s41598-022-26946-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Yipeng
Aghajan, Zahra M.
Ison, Matias
Lu, Qiujing
Tang, Hanlin
Kalender, Guldamla
Monsoor, Tonmoy
Zheng, Jie
Kreiman, Gabriel
Roychowdhury, Vwani
Fried, Itzhak
Decoding of human identity by computer vision and neuronal vision
title Decoding of human identity by computer vision and neuronal vision
title_full Decoding of human identity by computer vision and neuronal vision
title_fullStr Decoding of human identity by computer vision and neuronal vision
title_full_unstemmed Decoding of human identity by computer vision and neuronal vision
title_short Decoding of human identity by computer vision and neuronal vision
title_sort decoding of human identity by computer vision and neuronal vision
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837190/
https://www.ncbi.nlm.nih.gov/pubmed/36635322
http://dx.doi.org/10.1038/s41598-022-26946-w
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