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Exploring highly reliable substructures in auto-reconstructions of a neuron

The digital reconstruction of a neuron is the most direct and effective way to investigate its morphology. Many automatic neuron tracing methods have been proposed, but without manual check it is difficult to know whether a reconstruction or which substructure in a reconstruction is accurate. For a...

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Autores principales: He, Yishan, Huang, Jiajin, Wu, Gaowei, Yang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384950/
https://www.ncbi.nlm.nih.gov/pubmed/34431008
http://dx.doi.org/10.1186/s40708-021-00137-1
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author He, Yishan
Huang, Jiajin
Wu, Gaowei
Yang, Jian
author_facet He, Yishan
Huang, Jiajin
Wu, Gaowei
Yang, Jian
author_sort He, Yishan
collection PubMed
description The digital reconstruction of a neuron is the most direct and effective way to investigate its morphology. Many automatic neuron tracing methods have been proposed, but without manual check it is difficult to know whether a reconstruction or which substructure in a reconstruction is accurate. For a neuron’s reconstructions generated by multiple automatic tracing methods with different principles or models, their common substructures are highly reliable and named individual motifs. In this work, we propose a Vaa3D-based method called Lamotif to explore individual motifs in automatic reconstructions of a neuron. Lamotif utilizes the local alignment algorithm in BlastNeuron to extract local alignment pairs between a specified objective reconstruction and multiple reference reconstructions, and combines these pairs to generate individual motifs on the objective reconstruction. The proposed Lamotif is evaluated on reconstructions of 163 multiple species neurons, which are generated by four state-of-the-art tracing methods. Experimental results show that individual motifs are almost on corresponding gold standard reconstructions and have much higher precision rate than objective reconstructions themselves. Furthermore, an objective reconstruction is mostly quite accurate if its individual motifs have high recall rate. Individual motifs contain common geometry substructures in multiple reconstructions, and can be used to select some accurate substructures from a reconstruction or some accurate reconstructions from automatic reconstruction dataset of different neurons.
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spelling pubmed-83849502021-09-09 Exploring highly reliable substructures in auto-reconstructions of a neuron He, Yishan Huang, Jiajin Wu, Gaowei Yang, Jian Brain Inform Research The digital reconstruction of a neuron is the most direct and effective way to investigate its morphology. Many automatic neuron tracing methods have been proposed, but without manual check it is difficult to know whether a reconstruction or which substructure in a reconstruction is accurate. For a neuron’s reconstructions generated by multiple automatic tracing methods with different principles or models, their common substructures are highly reliable and named individual motifs. In this work, we propose a Vaa3D-based method called Lamotif to explore individual motifs in automatic reconstructions of a neuron. Lamotif utilizes the local alignment algorithm in BlastNeuron to extract local alignment pairs between a specified objective reconstruction and multiple reference reconstructions, and combines these pairs to generate individual motifs on the objective reconstruction. The proposed Lamotif is evaluated on reconstructions of 163 multiple species neurons, which are generated by four state-of-the-art tracing methods. Experimental results show that individual motifs are almost on corresponding gold standard reconstructions and have much higher precision rate than objective reconstructions themselves. Furthermore, an objective reconstruction is mostly quite accurate if its individual motifs have high recall rate. Individual motifs contain common geometry substructures in multiple reconstructions, and can be used to select some accurate substructures from a reconstruction or some accurate reconstructions from automatic reconstruction dataset of different neurons. Springer Berlin Heidelberg 2021-08-24 /pmc/articles/PMC8384950/ /pubmed/34431008 http://dx.doi.org/10.1186/s40708-021-00137-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Research
He, Yishan
Huang, Jiajin
Wu, Gaowei
Yang, Jian
Exploring highly reliable substructures in auto-reconstructions of a neuron
title Exploring highly reliable substructures in auto-reconstructions of a neuron
title_full Exploring highly reliable substructures in auto-reconstructions of a neuron
title_fullStr Exploring highly reliable substructures in auto-reconstructions of a neuron
title_full_unstemmed Exploring highly reliable substructures in auto-reconstructions of a neuron
title_short Exploring highly reliable substructures in auto-reconstructions of a neuron
title_sort exploring highly reliable substructures in auto-reconstructions of a neuron
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384950/
https://www.ncbi.nlm.nih.gov/pubmed/34431008
http://dx.doi.org/10.1186/s40708-021-00137-1
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