High-spatiotemporal-throughput video microscopy of freely moving organisms with diffractive multiplexing across a sensor array

Conventional microscopes exhibit a tradeoff among spatial resolution, field of view (FOV), and frame rate. To overcome this tradeoff, we designed a highly parallelized and multiplexed computational microscope that increases the spatiotemporal throughput by two orders of magnitude, achieving tens of gigapixels per second. Specifically, our microscope features a non-contiguous array of 48 camera sensors, with the information in the gaps multiplexed across the sensor array via an optimized diffractive pupil in a single synchronized snapshot. We applied our computational microscope to image dozens of freely-moving C. elegans in parallel at few-micron resolution over a multi-cm2 FOV at up to 40 fps.

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Publication Details

Published
2025-03-19
DOI
https://doi.org/10.1117/12.3042628
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
1.63
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article

High-spatiotemporal-throughput video microscopy of freely moving organisms with diffractive multiplexing across a sensor array

Kevin C. Zhou, Laura Waller, Saul Kato, Rajesh Menon et al.
1 citations
Advanced Fluorescence Microscopy Techniques
1.63
article

High-spatiotemporal-throughput video microscopy of freely moving organisms with diffractive multiplexing across a sensor array

Kevin C. Zhou, Laura Waller, Saul Kato, Rajesh Menon, Muneki Ikeda, Tina Hayward, Nicholas Antipa, Roarke Horstmeyer, Chaoying Gu
article en
1 citations

Abstract

Conventional microscopes exhibit a tradeoff among spatial resolution, field of view (FOV), and frame rate. To overcome this tradeoff, we designed a highly parallelized and multiplexed computational microscope that increases the spatiotemporal throughput by two orders of magnitude, achieving tens of gigapixels per second. Specifically, our microscope features a non-contiguous array of 48 camera sensors, with the information in the gaps multiplexed across the sensor array via an optimized diffractive pupil in a single synchronized snapshot. We applied our computational microscope to image dozens of freely-moving C. elegans in parallel at few-micron resolution over a multi-cm2 FOV at up to 40 fps.

Duke University (US), University of California, San Francisco (US), University of Utah (US), University of California San Diego (US), University of California, Berkeley (US)
Openalex Percentile: Top 16%
Advanced Fluorescence Microscopy Techniques
1.63
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High-spatiotemporal-throughput video microscopy of freely moving organisms with diffractive multiplexing across a sensor array — Kevin C. Zhou, Laura Waller, et al. · (2025) | TGRS Research Map | TGRS