COL0RME: Super-resolution microscopy based on sparse blinking/fluctuating fluorophore localization and intensity estimation. (16th February 2022)
- Record Type:
- Journal Article
- Title:
- COL0RME: Super-resolution microscopy based on sparse blinking/fluctuating fluorophore localization and intensity estimation. (16th February 2022)
- Main Title:
- COL0RME: Super-resolution microscopy based on sparse blinking/fluctuating fluorophore localization and intensity estimation
- Authors:
- Stergiopoulou, Vasiliki
Calatroni, Luca
de Morais Goulart, Henrique
Schaub, Sébastien
Blanc-Féraud, Laure - Abstract:
- Abstract: To overcome the physical barriers caused by light diffraction, super-resolution techniques are often applied in fluorescence microscopy. State-of-the-art approaches require specific and often demanding acquisition conditions to achieve adequate levels of both spatial and temporal resolution. Analyzing the stochastic fluctuations of the fluorescent molecules provides a solution to the aforementioned limitations, as sufficiently high spatio-temporal resolution for live-cell imaging can be achieved using common microscopes and conventional fluorescent dyes. Based on this idea, we present COL0RME, a method for covariance-based $ {\mathrm{\ell}}_0 $ super-resolution microscopy with intensity estimation, which achieves good spatio-temporal resolution by solving a sparse optimization problem in the covariance domain and discuss automatic parameter selection strategies. The method is composed of two steps: the former where both the emitters' independence and the sparse distribution of the fluorescent molecules are exploited to provide an accurate localization; the latter where real intensity values are estimated given the computed support. The paper is furnished with several numerical results both on synthetic and real fluorescence microscopy images and several comparisons with state-of-the art approaches are provided. Our results show that COL0RME outperforms competing methods exploiting analogously temporal fluctuations; in particular, it achieves better localization,Abstract: To overcome the physical barriers caused by light diffraction, super-resolution techniques are often applied in fluorescence microscopy. State-of-the-art approaches require specific and often demanding acquisition conditions to achieve adequate levels of both spatial and temporal resolution. Analyzing the stochastic fluctuations of the fluorescent molecules provides a solution to the aforementioned limitations, as sufficiently high spatio-temporal resolution for live-cell imaging can be achieved using common microscopes and conventional fluorescent dyes. Based on this idea, we present COL0RME, a method for covariance-based $ {\mathrm{\ell}}_0 $ super-resolution microscopy with intensity estimation, which achieves good spatio-temporal resolution by solving a sparse optimization problem in the covariance domain and discuss automatic parameter selection strategies. The method is composed of two steps: the former where both the emitters' independence and the sparse distribution of the fluorescent molecules are exploited to provide an accurate localization; the latter where real intensity values are estimated given the computed support. The paper is furnished with several numerical results both on synthetic and real fluorescence microscopy images and several comparisons with state-of-the art approaches are provided. Our results show that COL0RME outperforms competing methods exploiting analogously temporal fluctuations; in particular, it achieves better localization, reduces background artifacts, and avoids fine parameter tuning. … (more)
- Is Part Of:
- Biological imaging. Volume 2(2022)
- Journal:
- Biological imaging
- Issue:
- Volume 2(2022)
- Issue Display:
- Volume 2, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 2
- Issue:
- 2022
- Issue Sort Value:
- 2022-0002-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-02-16
- Subjects:
- Fluorescence microscopy -- SOFI method -- sparse optimization -- super-resolution
Imaging systems in biology -- Periodicals
570.28 - Journal URLs:
- https://www.cambridge.org/core/journals/biological-imaging ↗
- DOI:
- 10.1017/S2633903X22000010 ↗
- Languages:
- English
- ISSNs:
- 2633-903X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 21019.xml