ShapeMetrics: A userfriendly pipeline for 3D cell segmentation and spatial tissue analysis.
3D cell segmentation
Cell morphology analysis
Cell segmentation pipeline
Cell shape
Cell size
Ilastik
MATLAB
ShapeMetrics
Single cell analysis
Spatial localization
Tissue analysis
User-friendly code
Journal
Developmental biology
ISSN: 1095-564X
Titre abrégé: Dev Biol
Pays: United States
ID NLM: 0372762
Informations de publication
Date de publication:
01 06 2020
01 06 2020
Historique:
received:
13
08
2019
revised:
29
01
2020
accepted:
01
02
2020
pubmed:
18
2
2020
medline:
7
1
2021
entrez:
17
2
2020
Statut:
ppublish
Résumé
The demand for single-cell level data is constantly increasing within life sciences. In order to meet this demand, robust cell segmentation methods that can tackle challenging in vivo tissues with complex morphology are required. However, currently available cell segmentation and volumetric analysis methods perform poorly on 3D images. Here, we generated ShapeMetrics, a MATLAB-based script that segments cells in 3D and, by performing unbiased clustering using a heatmap, separates the cells into subgroups according to their volumetric and morphological differences. The cells can be accurately segregated according to different biologically meaningful features such as cell ellipticity, longest axis, cell elongation, or the ratio between cell volume and surface area. Our machine learning based script enables dissection of a large amount of novel data from microscope images in addition to the traditional information based on fluorescent biomarkers. Furthermore, the cells in different subgroups can be spatially mapped back to their original locations in the tissue image to help elucidate their roles in their respective morphological contexts. In order to facilitate the transition from bulk analysis to single-cell level accuracy, we emphasize the user-friendliness of our method by providing detailed step-by-step instructions through the pipeline hence aiming to reach users with less experience in computational biology.
Identifiants
pubmed: 32061886
pii: S0012-1606(20)30046-4
doi: 10.1016/j.ydbio.2020.02.003
pmc: PMC9624194
mid: NIHMS1836468
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Intramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
7-19Subventions
Organisme : Intramural NIH HHS
ID : ZIA DE000748
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIC DE000750
Pays : United States
Informations de copyright
Published by Elsevier Inc.
Références
Sci Rep. 2018 Jul 24;8(1):11135
pubmed: 30042482
Sci Rep. 2016 Aug 26;6:32412
pubmed: 27561654
Nature. 2010 Feb 18;463(7283):958-62
pubmed: 20130577
Source Code Biol Med. 2013 Aug 09;8(1):16
pubmed: 23938087
Development. 2018 Nov 19;145(22):
pubmed: 30333214
Front Physiol. 2018 Nov 12;9:1588
pubmed: 30483151
Nat Methods. 2017 Aug 31;14(9):849-863
pubmed: 28858338
Sci Rep. 2019 Mar 28;9(1):5302
pubmed: 30923332
J Vis Exp. 2014 Jul 08;(89):
pubmed: 25046278
PLoS Biol. 2018 Jul 3;16(7):e2005970
pubmed: 29969450
PLoS Genet. 2014 Mar 06;10(3):e1004193
pubmed: 24603431
Genome Biol. 2017 Nov 23;18(1):223
pubmed: 29169371
Stem Cell Reports. 2014 Mar 11;2(3):382-97
pubmed: 24672759
Semin Cell Dev Biol. 2012 May;23(3):320-32
pubmed: 22430756
Stem Cell Reports. 2018 Oct 9;11(4):912-928
pubmed: 30220628
Nat Commun. 2017 Nov 28;8(1):1830
pubmed: 29184067
Cell Rep. 2016 Dec 6;17(10):2648-2659
pubmed: 27926868
Methods Mol Biol. 2019;2002:151-163
pubmed: 30194538