The purpose of this study is to evaluate the various control parameters of a modeled fast non-local means (FNLM) noise reduction algorithm which can separate color channels in light microscopy (LM) images. To achieve this objective, the tendency of image characteristics with changes in parameters, such as smoothing factors and kernel and search window sizes for the FNLM algorithm, was analyzed. To quantitatively assess image characteristics, the coefficient of variation (COV), blind/referenceless image spatial quality evaluator (BRISQUE), and natural image quality evaluator (NIQE) were employed. When high smoothing factors and large search window sizes were applied, excellent COV and unsatisfactory BRISQUE and NIQE results were obtained. In addition, all three evaluation parameters improved as the kernel size increased. However, the kernel and search window sizes of the FNLM algorithm were shown to be dependent on the image processing time (time resolution). In conclusion, this work has demonstrated that the FNLM algorithm can effectively reduce noise in LM images, and parameter optimization is important to achieve the algorithm’s appropriate application.
1 September 2021 in Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
The purpose of this study was to propose a deep learning-based model for the super-resolution reconstruction of stained light microscopy images. To achieve this, perceptual loss was applied to the generator to reflect multichannel signal intensity, distribution, and structural similarity. A nested U-Net architecture was employed to address the representational limitations of the conventional U-Net. For quantitative evaluation, the peak signal-to-noise ratio (PSNR), structural similarity index (SSIM), and correlation coefficient (CC) were calculated. In addition, intensity profile analysis was performed to assess the model’s ability to restore the boundary signals more precisely. The experimental results demonstrated that the proposed model outperformed both the signal and structural restoration compared to single U-Net and U-Net-based generative adversarial network (GAN) models. Consequently, the PSNR, SSIM, and CC values demonstrated relative improvements of approximately 1.017, 1.023, and 1.010 times, respectively, compared to the input images. In particular, the intensity profile analysis confirmed the effectiveness of the nested U-Net-based generator in restoring cellular boundaries and structures in the stained microscopy images. In conclusion, the proposed model effectively enhanced the resolution of stained light microscopy images acquired in a multichannel format.
Diffusion-weighted magnetic resonance (DWMR) images were acquired using a custom-designed, 3D-printed breast-mimicking phantom. The smoothing factor of the non-local means (NLM) algorithm was then optimized for noise reduction. Phantoms were fabricated using polylactic acid, polyethylene terephthalate, and various concentrations of polyvinylpyrrolidone. DWMR images were obtained across b-values ranging from zero to 2000 s/mm2. Based on image contrast, the NLM algorithm was applied to the b = 1000 s/mm2 image, testing smoothing factors from 0.001 to 0.150. The NLM algorithm’s performance was quantitatively evaluated using a single DWMR image acquired from this custom phantom. At the optimized smoothing factor, the signal-to-noise ratio (SNR) improved from 96.87 ± 3.42 to 215.81 ± 4.18, and the contrast-to-noise ratio (CNR) from 43.63 ± 2.97 to 131.98 ± 3.56, representing 2.22-fold and 3.02-fold enhancements, respectively. No formal statistical tests were conducted as the analysis was based on a single acquisition. The optimized NLM algorithm also outperformed conventional denoising methods—median, Wiener, and total variation—in both noise suppression and contrast preservation. These findings suggest that the NLM algorithm with optimized parameters is likely to be more effective than existing approaches for enhancing breast DWMR image quality. However, further validation using in vivo patient datasets is essential to confirm its diagnostic utility and clinical generalizability because of the absence of tissue heterogeneity, motion, and physiological noise in the phantom environment.