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Elena Corbetta

Publications and source records attributed to Elena Corbetta.

3 recordsLinked to original sources

Physics-Informed Deep Learning Model for Cross-Modality Super-Resolution in Fluorescence Microscopy

Cross-modality image translation offers a route to super-resolution fluorescence microscopy from low-resolution images while reducing phototoxicity and instrumentation demands. However, purely data-driven models can produce visually plausible outputs that are inconsistent with optical image formation. Here, we propose a physics-informed generative adversarial network for confocal-to-STED image translation that incorporates microscope-specific point spread function information into the training objective. Simulated and experimentally measured PSFs were evaluated using a limited paired confocal-STED dataset of TOM20-labeled mitochondria in human primary M2 macrophages acquired across different experimental days. Performance was assessed using reference-based and non-reference-based image-quality metrics, together with complementary frequency- and distribution-sensitive analyses. The no-reference metrics probed physics-relevant image properties, including spatial-frequency content, contrast, and signal-to-noise behavior. PSF-guided models improved structural fidelity, reduced local deviations, and achieved closer agreement with STED references than non-PSF baselines, particularly in frequency-domain analyses. These results demonstrate that optical priors can improve the structural fidelity and physical plausibility of generative microscopy models for cross-modality super-resolution imaging.

cs.CV

Global-to-local image quality assessment in optical microscopy via fast and robust deep learning predictions

Optical microscopy is one of the most widely used techniques in research studies for life sciences and biomedicine. These applications require reliable experimental pipelines to extract valuable knowledge from the measured samples and must be supported by image quality assessment (IQA) to ensure correct processing and analysis of the image data. IQA methods are implemented with variable complexity. However, while most quality metrics have a straightforward implementation, they might be time consuming and computationally expensive when evaluating a large dataset. In addition, quality metrics are often designed for well-defined image features and may be unstable for images out of the ideal domain. To overcome these limitations, recent works have proposed deep learning-based IQA methods, which can provide superior performance, increased generalizability and fast prediction. Our method, named $\mathrm{\mu}$DeepIQA, is inspired by previous studies and applies a deep convolutional neural network designed for IQA on natural images to optical microscopy measurements. We retrained the same architecture to predict individual quality metrics and global quality scores for optical microscopy data. The resulting models provide fast and stable predictions of image quality by generalizing quality estimation even outside the ideal range of standard methods. In addition, $\mathrm{\mu}$DeepIQA provides patch-wise prediction of image quality and can be used to visualize spatially varying quality in a single image. Our study demonstrates that optical microscopy-based studies can benefit from the generalizability of deep learning models due to their stable performance in the presence of outliers, the ability to assess small image patches, and rapid predictions.

cs.CV

Multi-Marker Similarity enables reduced-reference and interpretable image quality assessment in optical microscopy

Optical microscopy contributes to the ever-increasing progress in biological and biomedical studies, as it allows the implementation of minimally invasive experimental pipelines to translate the data of measured samples into valuable knowledge. Within these pipelines, reliable quality assessment must be ensured to validate the generated results. Image quality assessment is often applied with full-reference methods to estimate the similarity between the ground truth and the output images. However, current methods often show poor agreement with visual perception and lead to the generation of various full-reference metrics tailored to specific applications. Additionally, they rely on pixel-wise comparisons, emphasizing local intensity similarity while often overlooking comprehensive and interpretable image quality assessment. To address these issues, we have developed a multi-marker similarity method that compares standard quality markers, such as resolution, signal-to-noise ratio, contrast, and high frequency components. The method computes a similarity score between the image and the ground truth for each marker, then combines these scores into an overall similarity estimate. This provides a full-reference estimate of image quality while extracting global quality features and detecting experimental artifacts. Multi-marker similarity provides a reliable and interpretable method for image quality assessment and the generation of quality rankings. By focusing on the comparison of quality markers rather than direct image distances, the method enables reduced reference implementations, where a single field of view is used as a benchmark for multiple measurements. This opens the way for reliable automatic evaluation of big datasets, typical of large biomedical studies, when manual assessment of single images and defining the ground truth for each field of view is not feasible.

q-bio.QM