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@ARTICLE{Uttenweiler:30346,
author = {Uttenweiler, D. and Weber, C. and Jähne, B. and Fink, R.
H. A. and Scharr, H.},
title = {{S}patiotemporal anisotropic diffusion filtering to improve
signal-to-noise ratios and object restoration in
fluorescence microscopic image sequences},
journal = {Journal of biomedical optics},
volume = {8},
issn = {1083-3668},
address = {Bellingham, Wash.},
publisher = {SPIE},
reportid = {PreJuSER-30346},
pages = {40 - 47},
year = {2003},
note = {Record converted from VDB: 12.11.2012},
abstract = {We present an approach for significantly improving the
quantitative analysis of motion in noisy fluorescence
microscopic image sequences. The new partial differential
equation based method is a general extension of a 2-D
nonlinear anisotropic diffusion filtering scheme to a
specially adapted 3-D nonlinear anisotropic diffusion
filtering scheme, with two spatial image dimensions and the
time t in the image sequence as the third dimension. Motion
in image sequences is considered as oriented, line-like
structures in the spatiotemporal x,y,t domain, which are
determined by the structure tensor method. Image enhancement
is achieved by a structure adopted smoothing kernel in three
dimensions, thereby using the full 3-D information inherent
in spatiotemporal image sequences. As an example for low
signal-to-noise ratio (SNR) microscopic image sequences we
have applied this method to noisy in vitro motility assay
data, where fluorescently labeled actin filaments move over
a surface of immobilized myosin. With the 3-D anisotropic
diffusion filtering the SNR is significantly improved (by a
factor of 3.8) and closed object structures are reliably
restored, which were originally degraded by noise.
Generally, this approach is very valuable for all
applications where motion has to be measured quantitatively
in low light level fluorescence microscopic image sequences
of cellular, subcellular, and molecular processes.},
keywords = {Actins: chemistry / Actins: ultrastructure / Animals /
Fluorescence Polarization: methods / Image Processing,
Computer-Assisted / Microscopy, Fluorescence: methods /
Motion / Rabbits / Actins (NLM Chemicals) / J (WoSType)},
cin = {ICG-III},
ddc = {530},
cid = {I:(DE-Juel1)VDB49},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
shelfmark = {Biochemical Research Methods / Optics / Radiology, Nuclear
Medicine $\&$ Medical Imaging},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:12542378},
UT = {WOS:000180755400005},
doi = {10.1117/1.1527627},
url = {https://juser.fz-juelich.de/record/30346},
}