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Moran’s I quantifies spatio-temporal pattern formation in neural imaging data
MOTIVATION: Neural activities of the brain occur through the formation of spatio-temporal patterns. In recent years, macroscopic neural imaging techniques have produced a large body of data on these patterned activities, yet a numerical measure of spatio-temporal coherence has often been reduced to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870747/ https://www.ncbi.nlm.nih.gov/pubmed/28575207 http://dx.doi.org/10.1093/bioinformatics/btx351 |
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author | Schmal, Christoph Myung, Jihwan Herzel, Hanspeter Bordyugov, Grigory |
author_facet | Schmal, Christoph Myung, Jihwan Herzel, Hanspeter Bordyugov, Grigory |
author_sort | Schmal, Christoph |
collection | PubMed |
description | MOTIVATION: Neural activities of the brain occur through the formation of spatio-temporal patterns. In recent years, macroscopic neural imaging techniques have produced a large body of data on these patterned activities, yet a numerical measure of spatio-temporal coherence has often been reduced to the global order parameter, which does not uncover the degree of spatial correlation. Here, we propose to use the spatial autocorrelation measure Moran’s I, which can be applied to capture dynamic signatures of spatial organization. We demonstrate the application of this technique to collective cellular circadian clock activities measured in the small network of the suprachiasmatic nucleus (SCN) in the hypothalamus. RESULTS: We found that Moran’s I is a practical quantitative measure of the degree of spatial coherence in neural imaging data. Initially developed with a geographical context in mind, Moran’s I accounts for the spatial organization of any interacting units. Moran’s I can be modified in accordance with the characteristic length scale of a neural activity pattern. It allows a quantification of statistical significance levels for the observed patterns. We describe the technique applied to synthetic datasets and various experimental imaging time-series from cultured SCN explants. It is demonstrated that major characteristics of the collective state can be described by Moran’s I and the traditional Kuramoto order parameter R in a complementary fashion. AVAILABILITY AND IMPLEMENTATION: Python 2.7 code of illustrative examples can be found in the Supplementary Material. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5870747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58707472018-04-05 Moran’s I quantifies spatio-temporal pattern formation in neural imaging data Schmal, Christoph Myung, Jihwan Herzel, Hanspeter Bordyugov, Grigory Bioinformatics Original Papers MOTIVATION: Neural activities of the brain occur through the formation of spatio-temporal patterns. In recent years, macroscopic neural imaging techniques have produced a large body of data on these patterned activities, yet a numerical measure of spatio-temporal coherence has often been reduced to the global order parameter, which does not uncover the degree of spatial correlation. Here, we propose to use the spatial autocorrelation measure Moran’s I, which can be applied to capture dynamic signatures of spatial organization. We demonstrate the application of this technique to collective cellular circadian clock activities measured in the small network of the suprachiasmatic nucleus (SCN) in the hypothalamus. RESULTS: We found that Moran’s I is a practical quantitative measure of the degree of spatial coherence in neural imaging data. Initially developed with a geographical context in mind, Moran’s I accounts for the spatial organization of any interacting units. Moran’s I can be modified in accordance with the characteristic length scale of a neural activity pattern. It allows a quantification of statistical significance levels for the observed patterns. We describe the technique applied to synthetic datasets and various experimental imaging time-series from cultured SCN explants. It is demonstrated that major characteristics of the collective state can be described by Moran’s I and the traditional Kuramoto order parameter R in a complementary fashion. AVAILABILITY AND IMPLEMENTATION: Python 2.7 code of illustrative examples can be found in the Supplementary Material. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-10-01 2017-05-31 /pmc/articles/PMC5870747/ /pubmed/28575207 http://dx.doi.org/10.1093/bioinformatics/btx351 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Schmal, Christoph Myung, Jihwan Herzel, Hanspeter Bordyugov, Grigory Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title | Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title_full | Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title_fullStr | Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title_full_unstemmed | Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title_short | Moran’s I quantifies spatio-temporal pattern formation in neural imaging data |
title_sort | moran’s i quantifies spatio-temporal pattern formation in neural imaging data |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870747/ https://www.ncbi.nlm.nih.gov/pubmed/28575207 http://dx.doi.org/10.1093/bioinformatics/btx351 |
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