ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data
Siewert Hugelier
1
,
Qing Tang
1
,
Hannah Hyun-Sook Kim
1, 2
,
Melina Theoni Gyparaki
3, 4
,
Charles Bond
1, 5
,
Adriana Naomi Santiago-Ruiz
1, 2
,
Sílvia Porta
6
,
M. Lakadamyali
1, 7
1
3
4
Vertex Pharmaceuticals, New York, USA
|
Publication type: Journal Article
Publication date: 2024-09-10
scimago Q1
wos Q1
SJR: 17.251
CiteScore: 49.0
Impact factor: 32.1
ISSN: 15487091, 15487105
PubMed ID:
39256629
Abstract
Single-molecule localization microscopy (SMLM) has gained widespread use for visualizing the morphology of subcellular organelles and structures with nanoscale spatial resolution. However, analysis tools for automatically quantifying and classifying SMLM images have lagged behind. Here we introduce Enhanced Classification of Localized Point clouds by Shape Extraction (ECLiPSE), an automated machine learning analysis pipeline specifically designed to classify cellular structures captured through two-dimensional or three-dimensional SMLM. ECLiPSE leverages a comprehensive set of shape descriptors, the majority of which are directly extracted from the localizations to minimize bias during the characterization of individual structures. ECLiPSE has been validated using both unsupervised and supervised classification on datasets, including various cellular structures, achieving near-perfect accuracy. We apply two-dimensional ECLiPSE to classify morphologically distinct protein aggregates relevant for neurodegenerative diseases. Additionally, we employ three-dimensional ECLiPSE to identify relevant biological differences between healthy and depolarized mitochondria. ECLiPSE will enhance the way we study cellular structures across various biological contexts. Enhanced Classification of Localized Point clouds by Shape Extraction (ECLiPSE) is a robust feature extraction and classification pipeline for diverse and heterogeneous structures in both 2D and 3D single-molecule localization microscopy data.
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10
Total citations:
10
Citations from 2024:
9
(100%)
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GOST
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Hugelier S. et al. ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data // Nature Methods. 2024. Vol. 21. No. 10. pp. 1909-1915.
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Hugelier S., Tang Q., Kim H. H., Gyparaki M. T., Bond C., Santiago-Ruiz A. N., Porta S., Lakadamyali M. ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data // Nature Methods. 2024. Vol. 21. No. 10. pp. 1909-1915.
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RIS
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TY - JOUR
DO - 10.1038/s41592-024-02414-3
UR - https://www.nature.com/articles/s41592-024-02414-3
TI - ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data
T2 - Nature Methods
AU - Hugelier, Siewert
AU - Tang, Qing
AU - Kim, Hannah Hyun-Sook
AU - Gyparaki, Melina Theoni
AU - Bond, Charles
AU - Santiago-Ruiz, Adriana Naomi
AU - Porta, Sílvia
AU - Lakadamyali, M.
PY - 2024
DA - 2024/09/10
PB - Springer Nature
SP - 1909-1915
IS - 10
VL - 21
PMID - 39256629
SN - 1548-7091
SN - 1548-7105
ER -
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BibTex (up to 50 authors)
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@article{2024_Hugelier,
author = {Siewert Hugelier and Qing Tang and Hannah Hyun-Sook Kim and Melina Theoni Gyparaki and Charles Bond and Adriana Naomi Santiago-Ruiz and Sílvia Porta and M. Lakadamyali},
title = {ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data},
journal = {Nature Methods},
year = {2024},
volume = {21},
publisher = {Springer Nature},
month = {sep},
url = {https://www.nature.com/articles/s41592-024-02414-3},
number = {10},
pages = {1909--1915},
doi = {10.1038/s41592-024-02414-3}
}
Cite this
MLA
Copy
Hugelier, Siewert, et al. “ECLiPSE: a versatile classification technique for structural and morphological analysis of 2D and 3D single-molecule localization microscopy data.” Nature Methods, vol. 21, no. 10, Sep. 2024, pp. 1909-1915. https://www.nature.com/articles/s41592-024-02414-3.