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SKOOTS: Skeleton oriented object segmentation for mitochondria
The segmentation of individual instances of mitochondria from imaging datasets is informative, yet time-consuming to do by hand, sparking interest in developing automated algorithms using deep neural networks. Existing solutions for various segmentation tasks are largely optimized for one of two typ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197543/ https://www.ncbi.nlm.nih.gov/pubmed/37214838 http://dx.doi.org/10.1101/2023.05.05.539611 |
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author | Buswinka, Christopher J Nitta, Hidetomi Osgood, Richard T. Indzhykulian, Artur A. |
author_facet | Buswinka, Christopher J Nitta, Hidetomi Osgood, Richard T. Indzhykulian, Artur A. |
author_sort | Buswinka, Christopher J |
collection | PubMed |
description | The segmentation of individual instances of mitochondria from imaging datasets is informative, yet time-consuming to do by hand, sparking interest in developing automated algorithms using deep neural networks. Existing solutions for various segmentation tasks are largely optimized for one of two types of biomedical imaging: high resolution three-dimensional (whole neuron segmentation in volumetric electron microscopy datasets) or two-dimensional low resolution (whole cell segmentation of light microscopy images). The former requires consistently predictable boundaries to segment large structures, while the latter is boundary invariant but struggles with segmentation of large 3D objects without downscaling. Mitochondria in whole cell 3D EM datasets often occupy the challenging middle ground: large with ambiguous borders, limiting accuracy with existing tools. To rectify this, we have developed skeleton oriented object segmentation (SKOOTS); a new segmentation approach which efficiently handles large, densely packed mitochondria. We show that SKOOTS can accurately, and efficiently, segment 3D mitochondria in previously difficult situations. Furthermore, we will release a new, manually annotated, 3D mitochondria segmentation dataset. Finally, we show this approach can be extended to segment objects in 3D light microscopy datasets. These results bridge the gap between existing segmentation approaches and increases the accessibility for three-dimensional biomedical image analysis. |
format | Online Article Text |
id | pubmed-10197543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101975432023-05-20 SKOOTS: Skeleton oriented object segmentation for mitochondria Buswinka, Christopher J Nitta, Hidetomi Osgood, Richard T. Indzhykulian, Artur A. bioRxiv Article The segmentation of individual instances of mitochondria from imaging datasets is informative, yet time-consuming to do by hand, sparking interest in developing automated algorithms using deep neural networks. Existing solutions for various segmentation tasks are largely optimized for one of two types of biomedical imaging: high resolution three-dimensional (whole neuron segmentation in volumetric electron microscopy datasets) or two-dimensional low resolution (whole cell segmentation of light microscopy images). The former requires consistently predictable boundaries to segment large structures, while the latter is boundary invariant but struggles with segmentation of large 3D objects without downscaling. Mitochondria in whole cell 3D EM datasets often occupy the challenging middle ground: large with ambiguous borders, limiting accuracy with existing tools. To rectify this, we have developed skeleton oriented object segmentation (SKOOTS); a new segmentation approach which efficiently handles large, densely packed mitochondria. We show that SKOOTS can accurately, and efficiently, segment 3D mitochondria in previously difficult situations. Furthermore, we will release a new, manually annotated, 3D mitochondria segmentation dataset. Finally, we show this approach can be extended to segment objects in 3D light microscopy datasets. These results bridge the gap between existing segmentation approaches and increases the accessibility for three-dimensional biomedical image analysis. Cold Spring Harbor Laboratory 2023-05-08 /pmc/articles/PMC10197543/ /pubmed/37214838 http://dx.doi.org/10.1101/2023.05.05.539611 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Buswinka, Christopher J Nitta, Hidetomi Osgood, Richard T. Indzhykulian, Artur A. SKOOTS: Skeleton oriented object segmentation for mitochondria |
title | SKOOTS: Skeleton oriented object segmentation for mitochondria |
title_full | SKOOTS: Skeleton oriented object segmentation for mitochondria |
title_fullStr | SKOOTS: Skeleton oriented object segmentation for mitochondria |
title_full_unstemmed | SKOOTS: Skeleton oriented object segmentation for mitochondria |
title_short | SKOOTS: Skeleton oriented object segmentation for mitochondria |
title_sort | skoots: skeleton oriented object segmentation for mitochondria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197543/ https://www.ncbi.nlm.nih.gov/pubmed/37214838 http://dx.doi.org/10.1101/2023.05.05.539611 |
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