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Quality of biological images, reconstructed using localization microscopy data
MOTIVATION: Fluorescence localization microscopy is extensively used to study the details of spatial architecture of subcellular compartments. This modality relies on determination of spatial positions of fluorophores, labeling an extended biological structure, with precision exceeding the diffracti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192211/ https://www.ncbi.nlm.nih.gov/pubmed/29028905 http://dx.doi.org/10.1093/bioinformatics/btx597 |
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author | Ruszczycki, Błażej Bernas, Tytus |
author_facet | Ruszczycki, Błażej Bernas, Tytus |
author_sort | Ruszczycki, Błażej |
collection | PubMed |
description | MOTIVATION: Fluorescence localization microscopy is extensively used to study the details of spatial architecture of subcellular compartments. This modality relies on determination of spatial positions of fluorophores, labeling an extended biological structure, with precision exceeding the diffraction limit. Several established models describe influence of pixel size, signal-to-noise ratio and optical resolution on the localization precision. The labeling density has been also recognized as important factor affecting reconstruction fidelity of the imaged biological structure. However, quantitative data on combined influence of sampling and localization errors on the fidelity of reconstruction are scarce. It should be noted that processing localization microscopy data is similar to reconstruction of a continuous (extended) non-periodic signal from a non-uniform, noisy point samples. In two dimensions the problem may be formulated within the framework of matrix completion. However, no systematic approach has been adopted in microscopy, where images are typically rendered by representing localized molecules with Gaussian distributions (widths determined by localization precision). RESULTS: We analyze the process of two-dimensional reconstruction of extended biological structures as a function of the density of registered emitters, localization precision and the area occupied by the rendered localized molecule. We quantify overall reconstruction fidelity with different established image similarity measures. Furthermore, we analyze the recovered similarity measure in the frequency space for different reconstruction protocols. We compare the cut-off frequency to the limiting sampling frequency, as determined by labeling density. AVAILABILITY AND IMPLEMENTATION: The source code used in the simulations along with test images is available at https://github.com/blazi13/qbioimages. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6192211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61922112019-03-01 Quality of biological images, reconstructed using localization microscopy data Ruszczycki, Błażej Bernas, Tytus Bioinformatics Original Papers MOTIVATION: Fluorescence localization microscopy is extensively used to study the details of spatial architecture of subcellular compartments. This modality relies on determination of spatial positions of fluorophores, labeling an extended biological structure, with precision exceeding the diffraction limit. Several established models describe influence of pixel size, signal-to-noise ratio and optical resolution on the localization precision. The labeling density has been also recognized as important factor affecting reconstruction fidelity of the imaged biological structure. However, quantitative data on combined influence of sampling and localization errors on the fidelity of reconstruction are scarce. It should be noted that processing localization microscopy data is similar to reconstruction of a continuous (extended) non-periodic signal from a non-uniform, noisy point samples. In two dimensions the problem may be formulated within the framework of matrix completion. However, no systematic approach has been adopted in microscopy, where images are typically rendered by representing localized molecules with Gaussian distributions (widths determined by localization precision). RESULTS: We analyze the process of two-dimensional reconstruction of extended biological structures as a function of the density of registered emitters, localization precision and the area occupied by the rendered localized molecule. We quantify overall reconstruction fidelity with different established image similarity measures. Furthermore, we analyze the recovered similarity measure in the frequency space for different reconstruction protocols. We compare the cut-off frequency to the limiting sampling frequency, as determined by labeling density. AVAILABILITY AND IMPLEMENTATION: The source code used in the simulations along with test images is available at https://github.com/blazi13/qbioimages. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-03-01 2017-09-25 /pmc/articles/PMC6192211/ /pubmed/29028905 http://dx.doi.org/10.1093/bioinformatics/btx597 Text en © The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Ruszczycki, Błażej Bernas, Tytus Quality of biological images, reconstructed using localization microscopy data |
title | Quality of biological images, reconstructed using localization microscopy
data |
title_full | Quality of biological images, reconstructed using localization microscopy
data |
title_fullStr | Quality of biological images, reconstructed using localization microscopy
data |
title_full_unstemmed | Quality of biological images, reconstructed using localization microscopy
data |
title_short | Quality of biological images, reconstructed using localization microscopy
data |
title_sort | quality of biological images, reconstructed using localization microscopy
data |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192211/ https://www.ncbi.nlm.nih.gov/pubmed/29028905 http://dx.doi.org/10.1093/bioinformatics/btx597 |
work_keys_str_mv | AT ruszczyckibłazej qualityofbiologicalimagesreconstructedusinglocalizationmicroscopydata AT bernastytus qualityofbiologicalimagesreconstructedusinglocalizationmicroscopydata |