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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4765885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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