SPARCOM: Sparsity Based Super-Resolution Correlation Microscopy
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Abstract (arXiv)
In traditional optical imaging systems, the spatial resolution is limited by the physics of diffraction, which acts as a low-pass filter. The information on sub-wavelength features is carried by evanescent waves, never reaching the camera, thereby posing a hard limit on resolution: the so-called diffraction limit. Modern microscopic methods enable super-resolution, by employing florescence techniques. State-of-the-art localization based fluorescence subwavelength imaging techniques such as PALM and STORM achieve sub-diffraction spatial resolution of several tens of nano-meters. However, they require tens of thousands of exposures, which limits their temporal resolution. We have recently proposed SPARCOM (sparsity based super-resolution correlation microscopy), which exploits the sparse nature of the fluorophores distribution, alongside a statistical prior of uncorrelated emissions, and showed that SPARCOM achieves spatial resolution comparable to PALM/STORM, while capturing the data hundreds of times faster. Here, we provide a detailed mathematical formulation of SPARCOM, which in turn leads to an efficient numerical implementation, suitable for large-scale problems. We further extend our method to a general framework for sparsity based super-resolution imaging, in which sparsity can be assumed in other domains such as wavelet or discrete-cosine, leading to improved reconstructions in a variety of physical settings.
Key facts. Cited by 6 papers in the map (data through 7 Oct 2026). First posted on arXiv 28 Jul 2017.
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Citing papers per year: 2021: 3; 2022: 0; 2023: 1; 2024: 1; 2025: 1.
6 papers.
- 2021Deep Unrolled Recovery in Sparse Biological Imagingcited by 9
- 2021Deep Algorithm Unrolling for Biomedical Imagingcited by 6
- 2023Fluctuation-based deconvolution in fluorescence microscopy using plug-and-play denoiserscited by 1
- 2024Self-STORM: Deep Unrolled Self-Supervised Learning for Super-Resolution Microscopycited by 1
- 2025Deep Learning Empowered Super-Resolution: A Comprehensive Survey and Future Prospectscited by 1
- 2021DeepCEL0 for 2D Single Molecule Localization in Fluorescence Microscopycited by 0
- 2025Deep Learning Empowered Super-Resolution: A Comprehensive Survey and Future Prospects19 Sep 2025
- 2024Self-STORM: Deep Unrolled Self-Supervised Learning for Super-Resolution Microscopy25 Mar 2024
- 2023Fluctuation-based deconvolution in fluorescence microscopy using plug-and-play denoisers20 Mar 2023
- 2021Deep Unrolled Recovery in Sparse Biological Imaging28 Sep 2021
- 2021Deep Algorithm Unrolling for Biomedical Imaging15 Aug 2021
- 2021DeepCEL0 for 2D Single Molecule Localization in Fluorescence Microscopy5 Jul 2021