A BaSiC tool for background and shading correction of optical microscopy images

Tingying Peng(Helmholtz Zentrum München), Kurt S. Thorn(University of California, San Francisco), Timm Schroeder(ETH Zurich), Lichao Wang(Helmholtz Zentrum München), Fabian J. Theis(Helmholtz Zentrum München), Carsten Marr(Helmholtz Zentrum München), Nassir Navab(Johns Hopkins University)
Nature Communications
June 8, 2017
Cited by 398Open Access
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Abstract

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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