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A fast fiducial marker tracking model for fully automatic alignment in electron tomography

MOTIVATION: Automatic alignment, especially fiducial marker-based alignment, has become increasingly important due to the high demand of subtomogram averaging and the rapid development of large-field electron microscopy. Among the alignment steps, fiducial marker tracking is a crucial one that deter...

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Detalles Bibliográficos
Autores principales: Han, Renmin, Zhang, Fa, Gao, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030832/
https://www.ncbi.nlm.nih.gov/pubmed/29069299
http://dx.doi.org/10.1093/bioinformatics/btx653
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author Han, Renmin
Zhang, Fa
Gao, Xin
author_facet Han, Renmin
Zhang, Fa
Gao, Xin
author_sort Han, Renmin
collection PubMed
description MOTIVATION: Automatic alignment, especially fiducial marker-based alignment, has become increasingly important due to the high demand of subtomogram averaging and the rapid development of large-field electron microscopy. Among the alignment steps, fiducial marker tracking is a crucial one that determines the quality of the final alignment. Yet, it is still a challenging problem to track the fiducial markers accurately and effectively in a fully automatic manner. RESULTS: In this paper, we propose a robust and efficient scheme for fiducial marker tracking. Firstly, we theoretically prove the upper bound of the transformation deviation of aligning the positions of fiducial markers on two micrographs by affine transformation. Secondly, we design an automatic algorithm based on the Gaussian mixture model to accelerate the procedure of fiducial marker tracking. Thirdly, we propose a divide-and-conquer strategy against lens distortions to ensure the reliability of our scheme. To our knowledge, this is the first attempt that theoretically relates the projection model with the tracking model. The real-world experimental results further support our theoretical bound and demonstrate the effectiveness of our algorithm. This work facilitates the fully automatic tracking for datasets with a massive number of fiducial markers. AVAILABILITY AND IMPLEMENTATION: The C/C ++ source code that implements the fast fiducial marker tracking is available at https://github.com/icthrm/gmm-marker-tracking. Markerauto 1.6 version or later (also integrated in the AuTom platform at http://ear.ict.ac.cn/) offers a complete implementation for fast alignment, in which fast fiducial marker tracking is available by the ‘-t’ option. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-60308322018-07-10 A fast fiducial marker tracking model for fully automatic alignment in electron tomography Han, Renmin Zhang, Fa Gao, Xin Bioinformatics Original Papers MOTIVATION: Automatic alignment, especially fiducial marker-based alignment, has become increasingly important due to the high demand of subtomogram averaging and the rapid development of large-field electron microscopy. Among the alignment steps, fiducial marker tracking is a crucial one that determines the quality of the final alignment. Yet, it is still a challenging problem to track the fiducial markers accurately and effectively in a fully automatic manner. RESULTS: In this paper, we propose a robust and efficient scheme for fiducial marker tracking. Firstly, we theoretically prove the upper bound of the transformation deviation of aligning the positions of fiducial markers on two micrographs by affine transformation. Secondly, we design an automatic algorithm based on the Gaussian mixture model to accelerate the procedure of fiducial marker tracking. Thirdly, we propose a divide-and-conquer strategy against lens distortions to ensure the reliability of our scheme. To our knowledge, this is the first attempt that theoretically relates the projection model with the tracking model. The real-world experimental results further support our theoretical bound and demonstrate the effectiveness of our algorithm. This work facilitates the fully automatic tracking for datasets with a massive number of fiducial markers. AVAILABILITY AND IMPLEMENTATION: The C/C ++ source code that implements the fast fiducial marker tracking is available at https://github.com/icthrm/gmm-marker-tracking. Markerauto 1.6 version or later (also integrated in the AuTom platform at http://ear.ict.ac.cn/) offers a complete implementation for fast alignment, in which fast fiducial marker tracking is available by the ‘-t’ option. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-03-01 2017-10-23 /pmc/articles/PMC6030832/ /pubmed/29069299 http://dx.doi.org/10.1093/bioinformatics/btx653 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Papers
Han, Renmin
Zhang, Fa
Gao, Xin
A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title_full A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title_fullStr A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title_full_unstemmed A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title_short A fast fiducial marker tracking model for fully automatic alignment in electron tomography
title_sort fast fiducial marker tracking model for fully automatic alignment in electron tomography
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030832/
https://www.ncbi.nlm.nih.gov/pubmed/29069299
http://dx.doi.org/10.1093/bioinformatics/btx653
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