TY - GEN
T1 - Multi-modal image fusion for multispectral super-resolution in microscopy
AU - Dey, Neel
AU - Li, Shijie
AU - Bermond, Katharina
AU - Heintzmann, Rainer
AU - Curcio, Christine A.
AU - Ach, Thomas
AU - Gerig, Guido
N1 - Publisher Copyright:
© COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.
PY - 2019
Y1 - 2019
N2 - Spectral imaging is a ubiquitous tool in modern biochemistry. Despite acquiring dozens to thousands of spectral channels, existing technology cannot capture spectral images at the same spatial resolution as structural microscopy. Due to partial voluming and low light exposure, spectral images are often difficult to interpret and analyze. This highlights a need to upsample the low-resolution spectral image by using spatial information contained in the high-resolution image, thereby creating a fused representation with high specificity both spatially and spectrally. In this paper, we propose a framework for the fusion of co-registered structural and spectral microscopy images to create super-resolved representations of spectral images. As a first application, we super-resolve spectral images of ex-vivo retinal tissue imaged with confocal laser scanning microscopy, by using spatial information from structured illumination microscopy. Second, we super-resolve mass spectroscopic images of mouse brain tissue, by using spatial information from high-resolution histology images. We present a systematic validation of model assumptions crucial towards maintaining the original nature of spectra and the applicability of super-resolution. Goodness-of-fit for spectral predictions are evaluated through functional R2 values, and the spatial quality of the super-resolved images are evaluated using normalized mutual information.
AB - Spectral imaging is a ubiquitous tool in modern biochemistry. Despite acquiring dozens to thousands of spectral channels, existing technology cannot capture spectral images at the same spatial resolution as structural microscopy. Due to partial voluming and low light exposure, spectral images are often difficult to interpret and analyze. This highlights a need to upsample the low-resolution spectral image by using spatial information contained in the high-resolution image, thereby creating a fused representation with high specificity both spatially and spectrally. In this paper, we propose a framework for the fusion of co-registered structural and spectral microscopy images to create super-resolved representations of spectral images. As a first application, we super-resolve spectral images of ex-vivo retinal tissue imaged with confocal laser scanning microscopy, by using spatial information from structured illumination microscopy. Second, we super-resolve mass spectroscopic images of mouse brain tissue, by using spatial information from high-resolution histology images. We present a systematic validation of model assumptions crucial towards maintaining the original nature of spectra and the applicability of super-resolution. Goodness-of-fit for spectral predictions are evaluated through functional R2 values, and the spatial quality of the super-resolved images are evaluated using normalized mutual information.
KW - Bayesian Optimization
KW - Confocal Laser Scanning Microscopy
KW - Image Fusion
KW - Imaging Mass Spectroscopy
KW - Multispectral Image Super-resolution
KW - Multispectral Imaging
KW - Structured Illumination Microscopy
UR - http://www.scopus.com/inward/record.url?scp=85068325681&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068325681&partnerID=8YFLogxK
U2 - 10.1117/12.2512598
DO - 10.1117/12.2512598
M3 - Conference contribution
AN - SCOPUS:85068325681
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2019
A2 - Angelini, Elsa D.
A2 - Angelini, Elsa D.
A2 - Angelini, Elsa D.
A2 - Landman, Bennett A.
PB - SPIE
T2 - Medical Imaging 2019: Image Processing
Y2 - 19 February 2019 through 21 February 2019
ER -