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A generic methodological framework for studying single cell motility in high-throughput time-lapse data

Motivation: Motility is a fundamental cellular attribute, which plays a major part in processes ranging from embryonic development to metastasis. Traditionally, single cell motility is often studied by live cell imaging. Yet, such studies were so far limited to low throughput. To systematically stud...

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Autores principales: Schoenauer Sebag, Alice, Plancade, Sandra, Raulet-Tomkiewicz, Céline, Barouki, Robert, Vert, Jean-Philippe, Walter, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765885/
https://www.ncbi.nlm.nih.gov/pubmed/26072499
http://dx.doi.org/10.1093/bioinformatics/btv225
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author Schoenauer Sebag, Alice
Plancade, Sandra
Raulet-Tomkiewicz, Céline
Barouki, Robert
Vert, Jean-Philippe
Walter, Thomas
author_facet Schoenauer Sebag, Alice
Plancade, Sandra
Raulet-Tomkiewicz, Céline
Barouki, Robert
Vert, Jean-Philippe
Walter, Thomas
author_sort Schoenauer Sebag, Alice
collection PubMed
description Motivation: Motility is a fundamental cellular attribute, which plays a major part in processes ranging from embryonic development to metastasis. Traditionally, single cell motility is often studied by live cell imaging. Yet, such studies were so far limited to low throughput. To systematically study cell motility at a large scale, we need robust methods to quantify cell trajectories in live cell imaging data. Results: The primary contribution of this article is to present Motility study Integrated Workflow (MotIW), a generic workflow for the study of single cell motility in high-throughput time-lapse screening data. It is composed of cell tracking, cell trajectory mapping to an original feature space and hit detection according to a new statistical procedure. We show that this workflow is scalable and demonstrates its power by application to simulated data, as well as large-scale live cell imaging data. This application enables the identification of an ontology of cell motility patterns in a fully unsupervised manner. Availability and implementation: Python code and examples are available online (http://cbio.ensmp.fr/∼aschoenauer/motiw.html) Contact: thomas.walter@mines-paristech.fr Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-47658852016-03-04 A generic methodological framework for studying single cell motility in high-throughput time-lapse data Schoenauer Sebag, Alice Plancade, Sandra Raulet-Tomkiewicz, Céline Barouki, Robert Vert, Jean-Philippe Walter, Thomas Bioinformatics Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Motivation: Motility is a fundamental cellular attribute, which plays a major part in processes ranging from embryonic development to metastasis. Traditionally, single cell motility is often studied by live cell imaging. Yet, such studies were so far limited to low throughput. To systematically study cell motility at a large scale, we need robust methods to quantify cell trajectories in live cell imaging data. Results: The primary contribution of this article is to present Motility study Integrated Workflow (MotIW), a generic workflow for the study of single cell motility in high-throughput time-lapse screening data. It is composed of cell tracking, cell trajectory mapping to an original feature space and hit detection according to a new statistical procedure. We show that this workflow is scalable and demonstrates its power by application to simulated data, as well as large-scale live cell imaging data. This application enables the identification of an ontology of cell motility patterns in a fully unsupervised manner. Availability and implementation: Python code and examples are available online (http://cbio.ensmp.fr/∼aschoenauer/motiw.html) Contact: thomas.walter@mines-paristech.fr Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2015-06-15 2015-06-10 /pmc/articles/PMC4765885/ /pubmed/26072499 http://dx.doi.org/10.1093/bioinformatics/btv225 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland
Schoenauer Sebag, Alice
Plancade, Sandra
Raulet-Tomkiewicz, Céline
Barouki, Robert
Vert, Jean-Philippe
Walter, Thomas
A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title_full A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title_fullStr A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title_full_unstemmed A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title_short A generic methodological framework for studying single cell motility in high-throughput time-lapse data
title_sort generic methodological framework for studying single cell motility in high-throughput time-lapse data
topic Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765885/
https://www.ncbi.nlm.nih.gov/pubmed/26072499
http://dx.doi.org/10.1093/bioinformatics/btv225
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