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Digital defocus aberration interference for automated optical microscopy
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  • Published: 24 April 2026

Digital defocus aberration interference for automated optical microscopy

  • Haowen Zhou  ORCID: orcid.org/0000-0003-0955-40101 na1,
  • Shi Zhao1 na1,
  • Yujie Fan2,
  • Zhenyu Dong  ORCID: orcid.org/0009-0003-4507-84931,
  • Oumeng Zhang  ORCID: orcid.org/0000-0001-7318-21301,
  • Viviana Gradinaru  ORCID: orcid.org/0000-0001-5868-348X2 &
  • …
  • Changhuei Yang  ORCID: orcid.org/0000-0001-8791-03541 

Nature Communications (2026) Cite this article

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Subjects

  • Microscopy
  • Optical imaging

Abstract

Automation in optical microscopy is critical for enabling high-throughput imaging across a wide range of biomedical applications. Among the essential components of automated systems, robust autofocusing plays a pivotal role in maintaining image quality for both single-plane and volumetric imaging. However, conventional autofocusing methods often struggle with implementation complexity, limited generalizability across sample types, incompatibility with thick specimens, and slow feedback. We observed that the digitally summed Fourier spectrum of two images acquired from two-angle illumination exhibits interference-like fringe modulation when the sample is defocused. These digital fringes correlate directly with defocus through a physics-based relation. Based on this principle, we developed an automatic, efficient, and generalizable defocus detection method termed digital defocus aberration interference (DAbI). Implemented with a simple two-LED setup, DAbI can quantify the defocus distance over a range of 443 times the depth-of-field for thin samples and 296 times for thick specimens. It can additionally extend the natural depth-of-field of the imaging system by 20-fold when integrated with complex-field imaging. We demonstrated the versatile applications of DAbI on brightfield, complex-field, refractive index, confocal, and widefield fluorescence imaging, establishing it as a promising solution for automated, high-throughput optical microscopy.

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Acknowledgements

H.Z., S.Z., Z.D., O.Z., and C.Y. are supported by Rothenberg Innovation Initiative (RI2) (award number A4188-Yang-3-A1) and the Heritage Medical Research Institute (HMRI) (award number HMRI-15-09-01). Y.F. is supported by the Caltech Chen Postdoc Innovator Grant (award number ENDOW.CHEN-1.CPIACY25). H.Z. thanks for the support of Caltech Schmidt Graduate Research Fellowship. We thank Dr. Shoma Nakagawa from Caltech for preparing the live mouse embryo samples. We thank Prof. Richard J. Cote and Prof. Mark Watson from the School of Medicine at Washington University in Saint Louis for providing human lung cancer specimens. SolidWorks models from Thorlabs Inc (part numbers: RMS20X-PF) were used in the illustration.

Author information

Author notes
  1. These authors contributed equally: Haowen Zhou, Shi Zhao.

Authors and Affiliations

  1. Department of Electrical Engineering, California Institute of Technology, Pasadena, CA, USA

    Haowen Zhou, Shi Zhao, Zhenyu Dong, Oumeng Zhang & Changhuei Yang

  2. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA

    Yujie Fan & Viviana Gradinaru

Authors
  1. Haowen Zhou
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  2. Shi Zhao
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  3. Yujie Fan
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  4. Zhenyu Dong
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  5. Oumeng Zhang
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  6. Viviana Gradinaru
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  7. Changhuei Yang
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Corresponding author

Correspondence to Haowen Zhou.

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Competing interests

The authors, H.Z., S.Z., and C.Y., declare the following competing interests: on July 2, 2025, the California Institute of Technology filed a provisional patent application (CIT-9339-P) for the DAbI method, which covered the concept, implementation, and applications of the DAbI method described here. The remaining authors declare no competing interests.

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Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Cite this article

Zhou, H., Zhao, S., Fan, Y. et al. Digital defocus aberration interference for automated optical microscopy. Nat Commun (2026). https://doi.org/10.1038/s41467-026-72287-x

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  • Received: 19 August 2025

  • Accepted: 13 April 2026

  • Published: 24 April 2026

  • DOI: https://doi.org/10.1038/s41467-026-72287-x

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