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A deep learning and novelty detection framework for rapid phenotyping in high-content screening

Supervised machine learning is a powerful and widely used method for analyzing high-content screening data. Despite its accuracy, efficiency, and versatility, supervised machine learning has drawbacks, most notably its dependence on a priori knowledge of expected phenotypes and time-consuming classi...

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Detalles Bibliográficos
Autores principales: Sommer, Christoph, Hoefler, Rudolf, Samwer, Matthias, Gerlich, Daniel W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687041/
https://www.ncbi.nlm.nih.gov/pubmed/28954863
http://dx.doi.org/10.1091/mbc.E17-05-0333
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author Sommer, Christoph
Hoefler, Rudolf
Samwer, Matthias
Gerlich, Daniel W.
author_facet Sommer, Christoph
Hoefler, Rudolf
Samwer, Matthias
Gerlich, Daniel W.
author_sort Sommer, Christoph
collection PubMed
description Supervised machine learning is a powerful and widely used method for analyzing high-content screening data. Despite its accuracy, efficiency, and versatility, supervised machine learning has drawbacks, most notably its dependence on a priori knowledge of expected phenotypes and time-consuming classifier training. We provide a solution to these limitations with CellCognition Explorer, a generic novelty detection and deep learning framework. Application to several large-scale screening data sets on nuclear and mitotic cell morphologies demonstrates that CellCognition Explorer enables discovery of rare phenotypes without user training, which has broad implications for improved assay development in high-content screening.
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spelling pubmed-56870412018-01-22 A deep learning and novelty detection framework for rapid phenotyping in high-content screening Sommer, Christoph Hoefler, Rudolf Samwer, Matthias Gerlich, Daniel W. Mol Biol Cell Articles Supervised machine learning is a powerful and widely used method for analyzing high-content screening data. Despite its accuracy, efficiency, and versatility, supervised machine learning has drawbacks, most notably its dependence on a priori knowledge of expected phenotypes and time-consuming classifier training. We provide a solution to these limitations with CellCognition Explorer, a generic novelty detection and deep learning framework. Application to several large-scale screening data sets on nuclear and mitotic cell morphologies demonstrates that CellCognition Explorer enables discovery of rare phenotypes without user training, which has broad implications for improved assay development in high-content screening. The American Society for Cell Biology 2017-11-07 /pmc/articles/PMC5687041/ /pubmed/28954863 http://dx.doi.org/10.1091/mbc.E17-05-0333 Text en © 2017 Sommer, Hoefler, et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Sommer, Christoph
Hoefler, Rudolf
Samwer, Matthias
Gerlich, Daniel W.
A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title_full A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title_fullStr A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title_full_unstemmed A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title_short A deep learning and novelty detection framework for rapid phenotyping in high-content screening
title_sort deep learning and novelty detection framework for rapid phenotyping in high-content screening
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687041/
https://www.ncbi.nlm.nih.gov/pubmed/28954863
http://dx.doi.org/10.1091/mbc.E17-05-0333
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