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Calatroni, L.

Publications and source records attributed to Calatroni, L..

2 recordsLinked to original sources

Independent noise realizations enable morphologically agnostic image reconstruction in single-photon-sensitive microscopy

Advances in single-photon sensitive detectors are rapidly expanding the adoption of photon-counting fluorescence microscopy. Under the Poisson photon-counting statistics, iterative Richardson-Lucy (RL) -type algorithms are statistically optimal for image deconvolution but suffers from a fundamental semi-convergent behaviour: prolonged iterations inevitably amplify noise, requiring heuristic early stopping or regularisation typically based on assumptions about object morphology. Here we present a morphology-agnostic regularisation framework for RL deconvolution that exploits independent noise realisations instead of structural object priors. Preserving the Poisson statistics of the acquisition process, we formulate the Regularized by Noise (RbN): a regularized variational framework and its corresponding iterative minimization algorithm that exploit the statistical consistency of independent noise realisations to distinguish reproducible image features from stochastic noise. The regularisation strength is selected automatically using the Poisson residual whiteness principle, resulting in a fully data-driven reconstruction without heuristic parameter tuning. Photon-timing-resolved systems naturally provide the independent noise realisations exploited by our framework, whereas computational photon splitting provides a statistically equivalent implementation for photon-counting systems. We validate the approach experimentally using photon-timing-resolved confocal microscopy and image scanning microscopy across eight morphologically distinct subcellular targets, and further demonstrate its applicability to photon-counting microscopes through computational photon splitting. Across imaging modalities, detector technologies, biological structures and signal-to-noise regimes, our method eliminates RL semi-convergence, removes sensitivity to the stopping criterion, and consistently outperforms conventional RL while preserving fine structural detail. More broadly, our results establish independent noise realisations as a general source of morphology-agnostic regularisation. Although demonstrated here for SPAD-based laser-scanning microscopy and Poisson statistics, the underlying principle could be extended to other imaging modalities and, more generally, to statistical inverse problems through appropriate noise-specific formulations.

biophysics↗

MUFASA: A Continuous-Time Stochastic Framework for Realistic Fluorescence Microscopy Simulation

We present MUFASA (Multi-Protocol Unified Fluorescence-based Advanced Simulation Algorithm), a physically grounded, continuous-time simulator for super-resolution fluorescence microscopy. By modeling fluorophore dynamics using continuous-time Markov chains, MUFASAs simulation features yield realistic photon emission behavior across both Single Molecule Localization Microscopy (SMLM) and fluorescence fluctuation-based (FF-SRM) protocols--independently of frame duration and sampling. The framework supports both individual emitters and structure-level simulations, incorporating photophysical transitions, photobleaching, and camera properties. To quantitatively validate simulations with real data, we introduce a novel validation metric based on the 1-Wasserstein distance between simulated and experimental photon-count distributions. In addition to simulation, another functionality estimates key photophysical parameters (e.g., molar extinction coefficient) and to suggest optimal light-source power ranges from fluctuation data. An intuitive Python-based graphical interface enables real-time parameter tuning, visualization, and TIFF export. Designed for biologists, physicists, microscopists, and numerical imaging engineers, MUFASA offers a practical platform for microscopy experiment design, hypothesis testing and the generation of realistic training data for data-driven microscopy methods across modalities.

biophysics↗