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ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations

Brightfield cell microscopy is a foundational tool in life sciences. The acquired images are prone to contain visual artifacts that hinder downstream analysis, and automatically removing them is therefore of great practical interest. Deep convolutional neural networks are state-of-the-art for image...

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Autores principales: Ali, Mohammed A. S., Hollo, Kaspar, Laasfeld, Tõnis, Torp, Jane, Tahk, Maris-Johanna, Rinken, Ago, Palo, Kaupo, Parts, Leopold, Fishman, Dmytro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259686/
https://www.ncbi.nlm.nih.gov/pubmed/35794119
http://dx.doi.org/10.1038/s41598-022-14703-y
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author Ali, Mohammed A. S.
Hollo, Kaspar
Laasfeld, Tõnis
Torp, Jane
Tahk, Maris-Johanna
Rinken, Ago
Palo, Kaupo
Parts, Leopold
Fishman, Dmytro
author_facet Ali, Mohammed A. S.
Hollo, Kaspar
Laasfeld, Tõnis
Torp, Jane
Tahk, Maris-Johanna
Rinken, Ago
Palo, Kaupo
Parts, Leopold
Fishman, Dmytro
author_sort Ali, Mohammed A. S.
collection PubMed
description Brightfield cell microscopy is a foundational tool in life sciences. The acquired images are prone to contain visual artifacts that hinder downstream analysis, and automatically removing them is therefore of great practical interest. Deep convolutional neural networks are state-of-the-art for image segmentation, but require pixel-level annotations, which are time-consuming to produce. Here, we propose ScoreCAM-U-Net, a pipeline to segment artifactual regions in brightfield images with limited user input. The model is trained using only image-level labels, so the process is faster by orders of magnitude compared to pixel-level annotation, but without substantially sacrificing the segmentation performance. We confirm that artifacts indeed exist with different shapes and sizes in three different brightfield microscopy image datasets, and distort downstream analyses such as nuclei segmentation, morphometry and fluorescence intensity quantification. We then demonstrate that our automated artifact removal ameliorates this problem. Such rapid cleaning of acquired images using the power of deep learning models is likely to become a standard step for all large scale microscopy experiments.
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spelling pubmed-92596862022-07-08 ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations Ali, Mohammed A. S. Hollo, Kaspar Laasfeld, Tõnis Torp, Jane Tahk, Maris-Johanna Rinken, Ago Palo, Kaupo Parts, Leopold Fishman, Dmytro Sci Rep Article Brightfield cell microscopy is a foundational tool in life sciences. The acquired images are prone to contain visual artifacts that hinder downstream analysis, and automatically removing them is therefore of great practical interest. Deep convolutional neural networks are state-of-the-art for image segmentation, but require pixel-level annotations, which are time-consuming to produce. Here, we propose ScoreCAM-U-Net, a pipeline to segment artifactual regions in brightfield images with limited user input. The model is trained using only image-level labels, so the process is faster by orders of magnitude compared to pixel-level annotation, but without substantially sacrificing the segmentation performance. We confirm that artifacts indeed exist with different shapes and sizes in three different brightfield microscopy image datasets, and distort downstream analyses such as nuclei segmentation, morphometry and fluorescence intensity quantification. We then demonstrate that our automated artifact removal ameliorates this problem. Such rapid cleaning of acquired images using the power of deep learning models is likely to become a standard step for all large scale microscopy experiments. Nature Publishing Group UK 2022-07-06 /pmc/articles/PMC9259686/ /pubmed/35794119 http://dx.doi.org/10.1038/s41598-022-14703-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Article
Ali, Mohammed A. S.
Hollo, Kaspar
Laasfeld, Tõnis
Torp, Jane
Tahk, Maris-Johanna
Rinken, Ago
Palo, Kaupo
Parts, Leopold
Fishman, Dmytro
ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title_full ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title_fullStr ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title_full_unstemmed ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title_short ArtSeg—Artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
title_sort artseg—artifact segmentation and removal in brightfield cell microscopy images without manual pixel-level annotations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259686/
https://www.ncbi.nlm.nih.gov/pubmed/35794119
http://dx.doi.org/10.1038/s41598-022-14703-y
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