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High-resolution data-driven model of the mouse connectome
Knowledge of mesoscopic brain connectivity is important for understanding inter- and intraregion information processing. Models of structural connectivity are typically constructed and analyzed with the assumption that regions are homogeneous. We instead use the Allen Mouse Brain Connectivity Atlas...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372022/ https://www.ncbi.nlm.nih.gov/pubmed/30793081 http://dx.doi.org/10.1162/netn_a_00066 |
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author | Knox, Joseph E. Harris, Kameron Decker Graddis, Nile Whitesell, Jennifer D. Zeng, Hongkui Harris, Julie A. Shea-Brown, Eric Mihalas, Stefan |
author_facet | Knox, Joseph E. Harris, Kameron Decker Graddis, Nile Whitesell, Jennifer D. Zeng, Hongkui Harris, Julie A. Shea-Brown, Eric Mihalas, Stefan |
author_sort | Knox, Joseph E. |
collection | PubMed |
description | Knowledge of mesoscopic brain connectivity is important for understanding inter- and intraregion information processing. Models of structural connectivity are typically constructed and analyzed with the assumption that regions are homogeneous. We instead use the Allen Mouse Brain Connectivity Atlas to construct a model of whole-brain connectivity at the scale of 100 μm voxels. The data consist of 428 anterograde tracing experiments in wild type C57BL/6J mice, mapping fluorescently labeled neuronal projections brain-wide. Inferring spatial connectivity with this dataset is underdetermined, since the approximately 2 × 10(5) source voxels outnumber the number of experiments. To address this issue, we assume that connection patterns and strengths vary smoothly across major brain divisions. We model the connectivity at each voxel as a radial basis kernel-weighted average of the projection patterns of nearby injections. The voxel model outperforms a previous regional model in predicting held-out experiments and compared with a human-curated dataset. This voxel-scale model of the mouse connectome permits researchers to extend their previous analyses of structural connectivity to much higher levels of resolution, and it allows for comparison with functional imaging and other datasets. |
format | Online Article Text |
id | pubmed-6372022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63720222019-02-21 High-resolution data-driven model of the mouse connectome Knox, Joseph E. Harris, Kameron Decker Graddis, Nile Whitesell, Jennifer D. Zeng, Hongkui Harris, Julie A. Shea-Brown, Eric Mihalas, Stefan Netw Neurosci Research Articles Knowledge of mesoscopic brain connectivity is important for understanding inter- and intraregion information processing. Models of structural connectivity are typically constructed and analyzed with the assumption that regions are homogeneous. We instead use the Allen Mouse Brain Connectivity Atlas to construct a model of whole-brain connectivity at the scale of 100 μm voxels. The data consist of 428 anterograde tracing experiments in wild type C57BL/6J mice, mapping fluorescently labeled neuronal projections brain-wide. Inferring spatial connectivity with this dataset is underdetermined, since the approximately 2 × 10(5) source voxels outnumber the number of experiments. To address this issue, we assume that connection patterns and strengths vary smoothly across major brain divisions. We model the connectivity at each voxel as a radial basis kernel-weighted average of the projection patterns of nearby injections. The voxel model outperforms a previous regional model in predicting held-out experiments and compared with a human-curated dataset. This voxel-scale model of the mouse connectome permits researchers to extend their previous analyses of structural connectivity to much higher levels of resolution, and it allows for comparison with functional imaging and other datasets. MIT Press 2018-12-01 /pmc/articles/PMC6372022/ /pubmed/30793081 http://dx.doi.org/10.1162/netn_a_00066 Text en © 2018 Massachusetts Institute of Technology 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 use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/legalcode. |
spellingShingle | Research Articles Knox, Joseph E. Harris, Kameron Decker Graddis, Nile Whitesell, Jennifer D. Zeng, Hongkui Harris, Julie A. Shea-Brown, Eric Mihalas, Stefan High-resolution data-driven model of the mouse connectome |
title | High-resolution data-driven model of the mouse connectome |
title_full | High-resolution data-driven model of the mouse connectome |
title_fullStr | High-resolution data-driven model of the mouse connectome |
title_full_unstemmed | High-resolution data-driven model of the mouse connectome |
title_short | High-resolution data-driven model of the mouse connectome |
title_sort | high-resolution data-driven model of the mouse connectome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372022/ https://www.ncbi.nlm.nih.gov/pubmed/30793081 http://dx.doi.org/10.1162/netn_a_00066 |
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