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Photon-free (s)CMOS camera characterization for artifact reduction in high- and super-resolution microscopy

Author

Listed:
  • Robin Diekmann

    (European Molecular Biology Laboratory (EMBL)
    LaVision Biotec GmbH)

  • Joran Deschamps

    (European Molecular Biology Laboratory (EMBL)
    Fondazione Human Technopole)

  • Yiming Li

    (European Molecular Biology Laboratory (EMBL)
    Southern University of Science and Technology)

  • Takahiro Deguchi

    (European Molecular Biology Laboratory (EMBL))

  • Aline Tschanz

    (European Molecular Biology Laboratory (EMBL)
    Collaboration for Joint PhD Degree Between EMBL and Heidelberg University, Faculty of Biosciences)

  • Maurice Kahnwald

    (European Molecular Biology Laboratory (EMBL)
    Friedrich Miescher Institute for Biomedical Research)

  • Ulf Matti

    (European Molecular Biology Laboratory (EMBL)
    Abberior Instruments GmbH)

  • Jonas Ries

    (European Molecular Biology Laboratory (EMBL))

Abstract

Modern implementations of widefield fluorescence microscopy often rely on sCMOS cameras, but this camera architecture inherently features pixel-to-pixel variations. Such variations lead to image artifacts and render quantitative image interpretation difficult. Although a variety of algorithmic corrections exists, they require a thorough characterization of the camera, which typically is not easy to access or perform. Here, we developed a fully automated pipeline for camera characterization based solely on thermally generated signal, and implemented it in the popular open-source software Micro-Manager and ImageJ/Fiji. Besides supplying the conventional camera maps of noise, offset and gain, our pipeline also gives access to dark current and thermal noise as functions of the exposure time. This allowed us to avoid structural bias in single-molecule localization microscopy (SMLM), which without correction is substantial even for scientific-grade, cooled cameras. In addition, our approach enables high-quality 3D super-resolution as well as live-cell time-lapse microscopy with cheap, industry-grade cameras. As our approach for camera characterization does not require any user interventions or additional hardware implementations, numerous correction algorithms that rely on camera characterization become easily applicable.

Suggested Citation

  • Robin Diekmann & Joran Deschamps & Yiming Li & Takahiro Deguchi & Aline Tschanz & Maurice Kahnwald & Ulf Matti & Jonas Ries, 2022. "Photon-free (s)CMOS camera characterization for artifact reduction in high- and super-resolution microscopy," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30907-2
    DOI: 10.1038/s41467-022-30907-2
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    References listed on IDEAS

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    1. Biagio Mandracchia & Xuanwen Hua & Changliang Guo & Jeonghwan Son & Tara Urner & Shu Jia, 2020. "Fast and accurate sCMOS noise correction for fluorescence microscopy," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
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    Cited by:

    1. Chang Qiao & Yunmin Zeng & Quan Meng & Xingye Chen & Haoyu Chen & Tao Jiang & Rongfei Wei & Jiabao Guo & Wenfeng Fu & Huaide Lu & Di Li & Yuwang Wang & Hui Qiao & Jiamin Wu & Dong Li & Qionghai Dai, 2024. "Zero-shot learning enables instant denoising and super-resolution in optical fluorescence microscopy," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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