Convolutional neural network denoising in fluorescence lifetime imaging microscopy (FLIM)

dc.contributor.authorMannam, Varun
dc.contributor.authorZhang, Yide
dc.contributor.authorYuan, Xiaotong
dc.contributor.authorHato, Takashi
dc.contributor.authorDagher, Pierre C.
dc.contributor.authorNichols, Evan L.
dc.contributor.authorSmith, Cody J.
dc.contributor.authorDunn, Kenneth W.
dc.contributor.authorHoward, Scott
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-08-14T11:08:02Z
dc.date.available2024-08-14T11:08:02Z
dc.date.issued2021
dc.description.abstractFluorescence lifetime imaging microscopy (FLIM) systems are limited by their slow processing speed, low signal- to-noise ratio (SNR), and expensive and challenging hardware setups. In this work, we demonstrate applying a denoising convolutional network to improve FLIM SNR. The network will integrated with an instant FLIM system with fast data acquisition based on analog signal processing, high SNR using high-efficiency pulse-modulation, and cost-effective implementation utilizing off-the-shelf radio-frequency components. Our instant FLIM system simultaneously provides the intensity, lifetime, and phasor plots in vivo and ex vivo. By integrating image de- noising using the trained deep learning model on the FLIM data, provide accurate FLIM phasor measurements are obtained. The enhanced phasor is then passed through the K-means clustering segmentation method, an unbiased and unsupervised machine learning technique to separate different fluorophores accurately. Our experimental in vivo mouse kidney results indicate that introducing the deep learning image denoising model before the segmentation effectively removes the noise in the phasor compared to existing methods and provides clearer segments. Hence, the proposed deep learning-based workflow provides fast and accurate automatic segmentation of fluorescence images using instant FLIM. The denoising operation is effective for the segmentation if the FLIM measurements are noisy. The clustering can effectively enhance the detection of biological structures of interest in biomedical imaging applications.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationMannam V, Zhang Y, Yuan X, et al. Convolutional neural network denoising in fluorescence lifetime imaging microscopy (FLIM). In: Multiphoton Microscopy in the Biomedical Sciences XXI. Vol 11648. SPIE; 2021:101-108. doi:10.1117/12.2578574
dc.identifier.urihttps://hdl.handle.net/1805/42778
dc.language.isoen_US
dc.publisherSPIE
dc.relation.isversionof10.1117/12.2578574
dc.relation.journalMultiphoton Microscopy in the Biomedical Sciences XXI
dc.rightsPublisher Policy
dc.sourceArXiv
dc.subjectFluorescence lifetime imaging
dc.subjectImage segmentation
dc.subjectMicroscopy
dc.subjectDenoising
dc.subjectIn vivo imaging
dc.subjectConvolutional neural networks
dc.subjectLuminescence
dc.titleConvolutional neural network denoising in fluorescence lifetime imaging microscopy (FLIM)
dc.typeArticle
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