2020
DOI: 10.1101/2020.12.02.408195
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Deep learning enables rapid and robust analysis of fluorescence lifetime imaging in photon-starved conditions

Abstract: Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool to quantify molecular compositions and study the molecular states in the complex cellular environment as the lifetime readings are not biased by the fluorophore concentration or the excitation power. However, the current methods to generate FLIM images are either computationally intensive or unreliable when the number of photons acquired at each pixel is low. Here we introduce a new deep learning-based method termed flimGANE (fluorescence lifet… Show more

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Cited by 4 publications
(2 citation statements)
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“…As NLSF was usually adopted in previous studies [ 25 , 27 , 35 ], we compared the inference performances of ELM and deconvolution-based NLSF (implemented with lsqcurvefit (·) function in MATLAB using iterative Levenberg–Marquardt algorithm) in Figure 2 . As such, 2000 simulated testing datasets were generated for recovery for single and double lifetimes.…”
Section: Synthetic Data Analysismentioning
confidence: 99%
“…As NLSF was usually adopted in previous studies [ 25 , 27 , 35 ], we compared the inference performances of ELM and deconvolution-based NLSF (implemented with lsqcurvefit (·) function in MATLAB using iterative Levenberg–Marquardt algorithm) in Figure 2 . As such, 2000 simulated testing datasets were generated for recovery for single and double lifetimes.…”
Section: Synthetic Data Analysismentioning
confidence: 99%
“…3-D [8] and 1-D CNNs [9] were proposed to process entire 3-D tensors and pixel-wise 1-D histograms, respectively. A generative adversarial network [10] was utilized in photon-starved conditions. Thanks to high hardware integration technologies, modern time-correlated singlephoton counting (TCSPC) systems [11] have been integrated on a single board.…”
Section: Introductionmentioning
confidence: 99%