A BaSiC tool for background and shading correction of optical microscopy images.
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Peng T
Department of Computer Science, Chair of Computer Aided Medical Procedure, Technische Universität München, Boltzmannstr. 3, Garching 85748, Germany.
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Thorn K
Department of Biochemistry and Biophysics, University of California, San Francisco, 600 16th Street, San Francisco, California 94158, USA.
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Schroeder T
Department of Biosystems Science and Engineering (D-BSSE), ETH Zurich, Basel 4058, Switzerland.
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Wang L
Department of Computer Science, Chair of Computer Aided Medical Procedure, Technische Universität München, Boltzmannstr. 3, Garching 85748, Germany.
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Theis FJ
Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Institute of Computational Biology, Ingolstädter Landstraße 1, Neuherberg 85764, Germany.
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Marr C
Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Institute of Computational Biology, Ingolstädter Landstraße 1, Neuherberg 85764, Germany.
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Navab N
Department of Computer Science, Chair of Computer Aided Medical Procedure, Technische Universität München, Boltzmannstr. 3, Garching 85748, Germany.
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Published in:
- Nature communications. - 2017
English
Quantitative analysis of bioimaging data is often skewed by both shading in space and background variation in time. We introduce BaSiC, an image correction method based on low-rank and sparse decomposition which solves both issues. In comparison to existing shading correction tools, BaSiC achieves high-accuracy with significantly fewer input images, works for diverse imaging conditions and is robust against artefacts. Moreover, it can correct temporal drift in time-lapse microscopy data and thus improve continuous single-cell quantification. BaSiC requires no manual parameter setting and is available as a Fiji/ImageJ plugin.
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Language
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Open access status
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gold
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Persistent URL
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https://sonar.ch/global/documents/217395
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