The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Deep learning enables cross-modality super-resolution in fluorescence microscopy
Open accessAbstract
We present deep-learning-enabled super-resolution across different fluorescence microscopy modalities. This data-driven approach does not require numerical modeling of the imaging process or the estimation of a point-spread-function, and is based on training a generative adversarial network (GAN) to transform diffraction-limited input images into super-resolved ones. Using this framework, we improve the resolution of wide-field images acquired with low-numerical-aperture objectives, matching the resolution that is acquired using high-numerical-aperture objectives. We also demonstrate cross-modality super-resolution, transforming confocal microscopy images to match the resolution acquired with a stimulated emission depletion (STED) microscope. We further demonstrate that total internal reflection fluorescence (TIRF) microscopy images of subcellular structures within cells and tissues can be transformed to match the results obtained with a TIRF-based structured illumination microscope. The deep network rapidly outputs these super-resolved images, without any iterations or parameter search, and could serve to democratize super-resolution imaging. Deep learning enables cross-modality super-resolution imaging, including confocal-to-STED and TIRF-to-TIRF-SIM image transformation. Imaging of a larger FOV and greater depth of field is possible with higher resolution and SNR at lower light doses.
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Moen, E., Bannon, D., Kudo, T., Graf, W., Covert, M., & Van Valen, D. (2019) · Nature Methods · doi:10.1038/s41592-019-0403-1 · Cited by 1,225
A survey on active learning and human-in-the-loop deep learning for medical image analysis
Budd, S., Robinson, E. C., & Kainz, B. (2021) · Medical Image Analysis · doi:10.1016/j.media.2021.102062 · Cited by 606
Modulating biomolecular condensates: a novel approach to drug discovery
Mitrea, D. M., Mittasch, M., Gomes, B. F., Klein, I. A., & Murcko, M. A. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00505-4 · Cited by 401
The ImageJ ecosystem: Open‐source software for image visualization, processing, and analysis
Schroeder, A. B., Dobson, E. T. A., Rueden, C. T., Tomancak, P., Jug, F., & Eliceiri, K. W. (2021) · Protein Science · doi:10.1002/pro.3993 · Cited by 391
Machine learning analysis of whole mouse brain vasculature
Todorov, M. I., Paetzold, J. C., Schoppe, O., Tetteh, G., Shit, S., Efremov, V., Todorov-Völgyi, K., Düring, M., Dichgans, M., Piraud, M., et al. (2020) · Nature Methods · doi:10.1038/s41592-020-0792-1 · Cited by 338
Metadata
- Authors
- Wang, H., Rivenson, Y., Jin, Y., Wei, Z., Gao, R., Günaydın, H., Bentolila, L. A., Kural, C., & Ozcan, A.
- Venue
- Nature Methods
- Published
- 2018-12-17
- Volume
- 16
- Issue
- 1
- Pages
- 103-110
- ISSN
- 1548-7091 (ISSN-L)
- 1548-7105
- OpenAlex
- W2904591139
- Cited by
- 782
- References
- 5
- FWCI
- 38.51
- Type
- journal article
- Language
- en
- Open access
- green
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