Target-to-Background Separation for Spectral Unmixing in In-Vivo Fluorescence Imaging
We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, w...
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Published in | Shanghai jiao tong da xue xue bao Vol. 19; no. 5; pp. 600 - 611 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Shanghai Jiaotong University Press
2014
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Subjects | |
Online Access | Get full text |
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Summary: | We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, we first enhance the intrinsic accumulation contrast in target-to-background fluorescence using h-dome transformation; then separate multi-target fluorescence areas from the background in sparse multispectral data utilizing kernel maximum auto- correlation factor analysis; we further use fast marching-based image inpainting method to patch up the removed target fluorescence areas and reconstruct the multispectral BF; with the BF matrix being subtracted from the original data, the multi-target fluorophores are easily unmixed from the subtracted data using multivariate curve resolution-alternating least squares method. In two preliminary in-vivo experiments, the proposed method demon- strated excellent performance to unmix multi-target fluorescences while other state-of-art unmixing methods failed to get desired results. |
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Bibliography: | fluorescence imaging, spectral unmixing, autofluorescence removal, target detection, kernel maxi-mum autocorrelation factor, target-to-background separation 31-1943/U We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, we first enhance the intrinsic accumulation contrast in target-to-background fluorescence using h-dome transformation; then separate multi-target fluorescence areas from the background in sparse multispectral data utilizing kernel maximum auto- correlation factor analysis; we further use fast marching-based image inpainting method to patch up the removed target fluorescence areas and reconstruct the multispectral BF; with the BF matrix being subtracted from the original data, the multi-target fluorophores are easily unmixed from the subtracted data using multivariate curve resolution-alternating least squares method. In two preliminary in-vivo experiments, the proposed method demon- strated excellent performance to unmix multi-target fluorescences while other state-of-art unmixing methods failed to get desired results. ZHAO Yong , HU Cheng , PENG Jin-liang, QIN Bin-jie (School of Biomedical Engineering, Shanghai Jiaotong University, Shanghai 200240, China) ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1007-1172 1995-8188 |
DOI: | 10.1007/s12204-014-1548-9 |