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ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy

The microscopy research at the Bionanoprobe (currently at beamline 9-ID and later 2-ID after APS-U) of Argonne National Laboratory focuses on applying synchrotron X-ray fluorescence (XRF) techniques to obtain trace elemental mappings of cryogenic biological samples to gain insights about their role...

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Autores principales: Chowdhury, M. A. Z., Ok, K., Luo, Y., Liu, Z., Chen, S., O’Halloran, T. V., Kettimuthu, R., Tekawade, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641565/
https://www.ncbi.nlm.nih.gov/pubmed/36345757
http://dx.doi.org/10.1107/S1600577522008876
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author Chowdhury, M. A. Z.
Ok, K.
Luo, Y.
Liu, Z.
Chen, S.
O’Halloran, T. V.
Kettimuthu, R.
Tekawade, A.
author_facet Chowdhury, M. A. Z.
Ok, K.
Luo, Y.
Liu, Z.
Chen, S.
O’Halloran, T. V.
Kettimuthu, R.
Tekawade, A.
author_sort Chowdhury, M. A. Z.
collection PubMed
description The microscopy research at the Bionanoprobe (currently at beamline 9-ID and later 2-ID after APS-U) of Argonne National Laboratory focuses on applying synchrotron X-ray fluorescence (XRF) techniques to obtain trace elemental mappings of cryogenic biological samples to gain insights about their role in critical biological activities. The elemental mappings and the morphological aspects of the biological samples, in this instance, the bacterium Escherichia coli (E. Coli), also serve as label-free biological fingerprints to identify E. coli cells that have been treated differently. The key limitations of achieving good identification performance are the extraction of cells from raw XRF measurements via binary conversion, definition of features, noise floor and proportion of cells treated differently in the measurement. Automating cell extraction from raw XRF measurements across different types of chemical treatment and the implementation of machine-learning models to distinguish cells from the background and their differing treatments are described. Principal components are calculated from domain knowledge specific features and clustered to distinguish healthy and poisoned cells from the background without manual annotation. The cells are ranked via fuzzy clustering to recommend regions of interest for automated experimentation. The effects of dwell time and the amount of data required on the usability of the software are also discussed.
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spelling pubmed-96415652022-11-14 ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy Chowdhury, M. A. Z. Ok, K. Luo, Y. Liu, Z. Chen, S. O’Halloran, T. V. Kettimuthu, R. Tekawade, A. J Synchrotron Radiat Computer Programs The microscopy research at the Bionanoprobe (currently at beamline 9-ID and later 2-ID after APS-U) of Argonne National Laboratory focuses on applying synchrotron X-ray fluorescence (XRF) techniques to obtain trace elemental mappings of cryogenic biological samples to gain insights about their role in critical biological activities. The elemental mappings and the morphological aspects of the biological samples, in this instance, the bacterium Escherichia coli (E. Coli), also serve as label-free biological fingerprints to identify E. coli cells that have been treated differently. The key limitations of achieving good identification performance are the extraction of cells from raw XRF measurements via binary conversion, definition of features, noise floor and proportion of cells treated differently in the measurement. Automating cell extraction from raw XRF measurements across different types of chemical treatment and the implementation of machine-learning models to distinguish cells from the background and their differing treatments are described. Principal components are calculated from domain knowledge specific features and clustered to distinguish healthy and poisoned cells from the background without manual annotation. The cells are ranked via fuzzy clustering to recommend regions of interest for automated experimentation. The effects of dwell time and the amount of data required on the usability of the software are also discussed. International Union of Crystallography 2022-10-25 /pmc/articles/PMC9641565/ /pubmed/36345757 http://dx.doi.org/10.1107/S1600577522008876 Text en © M. A. Z. Chowdhury et al. 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Computer Programs
Chowdhury, M. A. Z.
Ok, K.
Luo, Y.
Liu, Z.
Chen, S.
O’Halloran, T. V.
Kettimuthu, R.
Tekawade, A.
ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title_full ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title_fullStr ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title_full_unstemmed ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title_short ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy
title_sort roi-finder: machine learning to guide region-of-interest scanning for x-ray fluorescence microscopy
topic Computer Programs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641565/
https://www.ncbi.nlm.nih.gov/pubmed/36345757
http://dx.doi.org/10.1107/S1600577522008876
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