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3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo
BACKGROUND: Understanding the cellular architecture is a fundamental problem in various biological studies. C. elegans is widely used as a model organism in these studies because of its unique fate determinations. In recent years, researchers have worked extensively on C. elegans to excavate the reg...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454620/ https://www.ncbi.nlm.nih.gov/pubmed/30961566 http://dx.doi.org/10.1186/s12859-019-2720-x |
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author | Cao, Jianfeng Wong, Ming-Kin Zhao, Zhongying Yan, Hong |
author_facet | Cao, Jianfeng Wong, Ming-Kin Zhao, Zhongying Yan, Hong |
author_sort | Cao, Jianfeng |
collection | PubMed |
description | BACKGROUND: Understanding the cellular architecture is a fundamental problem in various biological studies. C. elegans is widely used as a model organism in these studies because of its unique fate determinations. In recent years, researchers have worked extensively on C. elegans to excavate the regulations of genes and proteins on cell mobility and communication. Although various algorithms have been proposed to analyze nucleus, cell shape features are not yet well recorded. This paper proposes a method to systematically analyze three-dimensional morphological cellular features. RESULTS: Three-dimensional Membrane Morphological Segmentation (3DMMS) makes use of several novel techniques, such as statistical intensity normalization, and region filters, to pre-process the cell images. We then segment membrane stacks based on watershed algorithms. 3DMMS achieves high robustness and precision over different time points (development stages). It is compared with two state-of-the-art algorithms, RACE and BCOMS. Quantitative analysis shows 3DMMS performs best with the average Dice ratio of 97.7% at six time points. In addition, 3DMMS also provides time series of internal and external shape features of C. elegans. CONCLUSION: We have developed the 3DMMS based technique for embryonic shape reconstruction at the single-cell level. With cells accurately segmented, 3DMMS makes it possible to study cellular shapes and bridge morphological features and biological expression in embryo research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2720-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6454620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64546202019-04-19 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo Cao, Jianfeng Wong, Ming-Kin Zhao, Zhongying Yan, Hong BMC Bioinformatics Methodology Article BACKGROUND: Understanding the cellular architecture is a fundamental problem in various biological studies. C. elegans is widely used as a model organism in these studies because of its unique fate determinations. In recent years, researchers have worked extensively on C. elegans to excavate the regulations of genes and proteins on cell mobility and communication. Although various algorithms have been proposed to analyze nucleus, cell shape features are not yet well recorded. This paper proposes a method to systematically analyze three-dimensional morphological cellular features. RESULTS: Three-dimensional Membrane Morphological Segmentation (3DMMS) makes use of several novel techniques, such as statistical intensity normalization, and region filters, to pre-process the cell images. We then segment membrane stacks based on watershed algorithms. 3DMMS achieves high robustness and precision over different time points (development stages). It is compared with two state-of-the-art algorithms, RACE and BCOMS. Quantitative analysis shows 3DMMS performs best with the average Dice ratio of 97.7% at six time points. In addition, 3DMMS also provides time series of internal and external shape features of C. elegans. CONCLUSION: We have developed the 3DMMS based technique for embryonic shape reconstruction at the single-cell level. With cells accurately segmented, 3DMMS makes it possible to study cellular shapes and bridge morphological features and biological expression in embryo research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2720-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-08 /pmc/articles/PMC6454620/ /pubmed/30961566 http://dx.doi.org/10.1186/s12859-019-2720-x Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Cao, Jianfeng Wong, Ming-Kin Zhao, Zhongying Yan, Hong 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title | 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title_full | 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title_fullStr | 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title_full_unstemmed | 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title_short | 3DMMS: robust 3D Membrane Morphological Segmentation of C. elegans embryo |
title_sort | 3dmms: robust 3d membrane morphological segmentation of c. elegans embryo |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454620/ https://www.ncbi.nlm.nih.gov/pubmed/30961566 http://dx.doi.org/10.1186/s12859-019-2720-x |
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