LimeSeg: a coarse-grained lipid membrane simulation for 3D image segmentation.

3D segmentation Cell membrane segmentation Cell surface Cell volume ImageJ Point-cloud Surfel-based

Journal

BMC bioinformatics
ISSN: 1471-2105
Titre abrégé: BMC Bioinformatics
Pays: England
ID NLM: 100965194

Informations de publication

Date de publication:
03 Jan 2019
Historique:
received: 17 04 2018
accepted: 06 11 2018
entrez: 5 1 2019
pubmed: 5 1 2019
medline: 14 2 2019
Statut: epublish

Résumé

3D segmentation is often a prerequisite for 3D object display and quantitative measurements. Yet existing voxel-based methods do not directly give information on the object surface or topology. As for spatially continuous approaches such as level-set, active contours and meshes, although providing surfaces and concise shape description, they are generally not suitable for multiple object segmentation and/or for objects with an irregular shape, which can hamper their adoption by bioimage analysts. We developed LimeSeg, a computationally efficient and spatially continuous 3D segmentation method. LimeSeg is easy-to-use and can process many and/or highly convoluted objects. Based on the concept of SURFace ELements ("Surfels"), LimeSeg resembles a highly coarse-grained simulation of a lipid membrane in which a set of particles, analogous to lipid molecules, are attracted to local image maxima. The particles are self-generating and self-destructing thus providing the ability for the membrane to evolve towards the contour of the objects of interest. The capabilities of LimeSeg: simultaneous segmentation of numerous non overlapping objects, segmentation of highly convoluted objects and robustness for big datasets are demonstrated on experimental use cases (epithelial cells, brain MRI and FIB-SEM dataset of cellular membrane system respectively). In conclusion, we implemented a new and efficient 3D surface reconstruction plugin adapted for various sources of images, which is deployed in the user-friendly and well-known ImageJ environment.

Sections du résumé

BACKGROUND BACKGROUND
3D segmentation is often a prerequisite for 3D object display and quantitative measurements. Yet existing voxel-based methods do not directly give information on the object surface or topology. As for spatially continuous approaches such as level-set, active contours and meshes, although providing surfaces and concise shape description, they are generally not suitable for multiple object segmentation and/or for objects with an irregular shape, which can hamper their adoption by bioimage analysts.
RESULTS RESULTS
We developed LimeSeg, a computationally efficient and spatially continuous 3D segmentation method. LimeSeg is easy-to-use and can process many and/or highly convoluted objects. Based on the concept of SURFace ELements ("Surfels"), LimeSeg resembles a highly coarse-grained simulation of a lipid membrane in which a set of particles, analogous to lipid molecules, are attracted to local image maxima. The particles are self-generating and self-destructing thus providing the ability for the membrane to evolve towards the contour of the objects of interest. The capabilities of LimeSeg: simultaneous segmentation of numerous non overlapping objects, segmentation of highly convoluted objects and robustness for big datasets are demonstrated on experimental use cases (epithelial cells, brain MRI and FIB-SEM dataset of cellular membrane system respectively).
CONCLUSION CONCLUSIONS
In conclusion, we implemented a new and efficient 3D surface reconstruction plugin adapted for various sources of images, which is deployed in the user-friendly and well-known ImageJ environment.

Identifiants

pubmed: 30606118
doi: 10.1186/s12859-018-2471-0
pii: 10.1186/s12859-018-2471-0
pmc: PMC6318983
doi:

Substances chimiques

Lipids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2

Subventions

Organisme : FP7 People: Marie-Curie Actions
ID : 300532-2011

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Auteurs

Sarah Machado (S)

Marcos González Gaitán lab, University of Geneva, Department of Biochemistry, quai Ernest-Ansermet 30, Geneva, 1211, Switzerland.

Vincent Mercier (V)

Aurélien Roux lab, University of Geneva, Department of Biochemistry, quai Ernest-Ansermet 30, Geneva, 1211, Switzerland.

Nicolas Chiaruttini (N)

Aurélien Roux lab, University of Geneva, Department of Biochemistry, quai Ernest-Ansermet 30, Geneva, 1211, Switzerland. nicolas.chiaruttini@unige.ch.

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Classifications MeSH