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Joint registration of multiple point clouds for fast particle fusion in localization microscopy

SUMMARY: We present a fast particle fusion method for particles imaged with single-molecule localization microscopy. The state-of-the-art approach based on all-to-all registration has proven to work well but its computational cost scales unfavorably with the number of particles N, namely as N(2). Ou...

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Autores principales: Wang, Wenxiu, Heydarian, Hamidreza, Huijben, Teun A P M, Stallinga, Sjoerd, Rieger, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9191212/
https://www.ncbi.nlm.nih.gov/pubmed/35552632
http://dx.doi.org/10.1093/bioinformatics/btac320
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author Wang, Wenxiu
Heydarian, Hamidreza
Huijben, Teun A P M
Stallinga, Sjoerd
Rieger, Bernd
author_facet Wang, Wenxiu
Heydarian, Hamidreza
Huijben, Teun A P M
Stallinga, Sjoerd
Rieger, Bernd
author_sort Wang, Wenxiu
collection PubMed
description SUMMARY: We present a fast particle fusion method for particles imaged with single-molecule localization microscopy. The state-of-the-art approach based on all-to-all registration has proven to work well but its computational cost scales unfavorably with the number of particles N, namely as N(2). Our method overcomes this problem and achieves a linear scaling of computational cost with N by making use of the Joint Registration of Multiple Point Clouds (JRMPC) method. Straightforward application of JRMPC fails as mostly locally optimal solutions are found. These usually contain several overlapping clusters that each consist of well-aligned particles, but that have different poses. We solve this issue by repeated runs of JRMPC for different initial conditions, followed by a classification step to identify the clusters, and a connection step to link the different clusters obtained for different initializations. In this way a single well-aligned structure is obtained containing the majority of the particles. RESULTS: We achieve reconstructions of experimental DNA-origami datasets consisting of close to 400 particles within only 10 min on a CPU, with an image resolution of 3.2 nm. In addition, we show artifact-free reconstructions of symmetric structures without making any use of the symmetry. We also demonstrate that the method works well for poor data with a low density of labeling and for 3D data. AVAILABILITY AND IMPLEMENTATION: The code is available for download from https://github.com/wexw/Joint-Registration-of-Multiple-Point-Clouds-for-Fast-Particle-Fusion-in-Localization-Microscopy. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-91912122022-06-14 Joint registration of multiple point clouds for fast particle fusion in localization microscopy Wang, Wenxiu Heydarian, Hamidreza Huijben, Teun A P M Stallinga, Sjoerd Rieger, Bernd Bioinformatics Original Papers SUMMARY: We present a fast particle fusion method for particles imaged with single-molecule localization microscopy. The state-of-the-art approach based on all-to-all registration has proven to work well but its computational cost scales unfavorably with the number of particles N, namely as N(2). Our method overcomes this problem and achieves a linear scaling of computational cost with N by making use of the Joint Registration of Multiple Point Clouds (JRMPC) method. Straightforward application of JRMPC fails as mostly locally optimal solutions are found. These usually contain several overlapping clusters that each consist of well-aligned particles, but that have different poses. We solve this issue by repeated runs of JRMPC for different initial conditions, followed by a classification step to identify the clusters, and a connection step to link the different clusters obtained for different initializations. In this way a single well-aligned structure is obtained containing the majority of the particles. RESULTS: We achieve reconstructions of experimental DNA-origami datasets consisting of close to 400 particles within only 10 min on a CPU, with an image resolution of 3.2 nm. In addition, we show artifact-free reconstructions of symmetric structures without making any use of the symmetry. We also demonstrate that the method works well for poor data with a low density of labeling and for 3D data. AVAILABILITY AND IMPLEMENTATION: The code is available for download from https://github.com/wexw/Joint-Registration-of-Multiple-Point-Clouds-for-Fast-Particle-Fusion-in-Localization-Microscopy. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-05-13 /pmc/articles/PMC9191212/ /pubmed/35552632 http://dx.doi.org/10.1093/bioinformatics/btac320 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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
Wang, Wenxiu
Heydarian, Hamidreza
Huijben, Teun A P M
Stallinga, Sjoerd
Rieger, Bernd
Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title_full Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title_fullStr Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title_full_unstemmed Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title_short Joint registration of multiple point clouds for fast particle fusion in localization microscopy
title_sort joint registration of multiple point clouds for fast particle fusion in localization microscopy
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9191212/
https://www.ncbi.nlm.nih.gov/pubmed/35552632
http://dx.doi.org/10.1093/bioinformatics/btac320
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