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Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction
Histological brain slices are widely used in neuroscience to study the anatomical organization of neural circuits. Systematic and accurate comparisons of anatomical data from multiple brains, especially from different studies, can benefit tremendously from registering histological slices onto a comm...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297281/ https://www.ncbi.nlm.nih.gov/pubmed/30618698 http://dx.doi.org/10.3389/fninf.2018.00093 |
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author | Xiong, Jing Ren, Jing Luo, Liqun Horowitz, Mark |
author_facet | Xiong, Jing Ren, Jing Luo, Liqun Horowitz, Mark |
author_sort | Xiong, Jing |
collection | PubMed |
description | Histological brain slices are widely used in neuroscience to study the anatomical organization of neural circuits. Systematic and accurate comparisons of anatomical data from multiple brains, especially from different studies, can benefit tremendously from registering histological slices onto a common reference atlas. Most existing methods rely on an initial reconstruction of the volume before registering it to a reference atlas. Because these slices are prone to distortions during the sectioning process and often sectioned with non-standard angles, reconstruction is challenging and often inaccurate. Here we describe a framework that maps each slice to its corresponding plane in the Allen Mouse Brain Atlas (2015) to build a plane-wise mapping and then perform 2D nonrigid registration to build a pixel-wise mapping. We use the L2 norm of the histogram of oriented gradients difference of two patches as the similarity metric for both steps and a Markov random field formulation that incorporates tissue coherency to compute the nonrigid registration. To fix significantly distorted regions that are misshaped or much smaller than the control grids, we train a context-aggregation network to segment and warp them to their corresponding regions with thin plate spline. We have shown that our method generates results comparable to an expert neuroscientist and is significantly better than reconstruction-first approaches. Code and sample dataset are available at sites.google.com/view/brain-mapping. |
format | Online Article Text |
id | pubmed-6297281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62972812019-01-07 Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction Xiong, Jing Ren, Jing Luo, Liqun Horowitz, Mark Front Neuroinform ICT Histological brain slices are widely used in neuroscience to study the anatomical organization of neural circuits. Systematic and accurate comparisons of anatomical data from multiple brains, especially from different studies, can benefit tremendously from registering histological slices onto a common reference atlas. Most existing methods rely on an initial reconstruction of the volume before registering it to a reference atlas. Because these slices are prone to distortions during the sectioning process and often sectioned with non-standard angles, reconstruction is challenging and often inaccurate. Here we describe a framework that maps each slice to its corresponding plane in the Allen Mouse Brain Atlas (2015) to build a plane-wise mapping and then perform 2D nonrigid registration to build a pixel-wise mapping. We use the L2 norm of the histogram of oriented gradients difference of two patches as the similarity metric for both steps and a Markov random field formulation that incorporates tissue coherency to compute the nonrigid registration. To fix significantly distorted regions that are misshaped or much smaller than the control grids, we train a context-aggregation network to segment and warp them to their corresponding regions with thin plate spline. We have shown that our method generates results comparable to an expert neuroscientist and is significantly better than reconstruction-first approaches. Code and sample dataset are available at sites.google.com/view/brain-mapping. Frontiers Media S.A. 2018-12-11 /pmc/articles/PMC6297281/ /pubmed/30618698 http://dx.doi.org/10.3389/fninf.2018.00093 Text en Copyright © 2018 Xiong, Ren, Luo and Horowitz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | ICT Xiong, Jing Ren, Jing Luo, Liqun Horowitz, Mark Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title | Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title_full | Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title_fullStr | Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title_full_unstemmed | Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title_short | Mapping Histological Slice Sequences to the Allen Mouse Brain Atlas Without 3D Reconstruction |
title_sort | mapping histological slice sequences to the allen mouse brain atlas without 3d reconstruction |
topic | ICT |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297281/ https://www.ncbi.nlm.nih.gov/pubmed/30618698 http://dx.doi.org/10.3389/fninf.2018.00093 |
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