Super-resolution time-resolved imaging using computational sensor fusion

被引:16
作者
Callenberg, C. [1 ]
Lyons, A. [2 ]
den Brok, D. [1 ]
Fatima, A. [2 ]
Turpin, A. [3 ]
Zickus, V. [2 ]
Machesky, L. [4 ]
Whitelaw, J. [4 ]
Faccio, D. [2 ]
Hullin, M. B. [1 ]
机构
[1] Univ Bonn, Inst Comp Sci, Bonn, Germany
[2] Univ Glasgow, Sch Phys & Astron, Glasgow G12 8QQ, Lanark, Scotland
[3] Univ Glasgow, Sch Comp Sci, Glasgow G12 8LT, Lanark, Scotland
[4] Beatson Inst, Canc Res UK, Glasgow, Lanark, Scotland
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
D O I
10.1038/s41598-021-81159-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Imaging across both the full transverse spatial and temporal dimensions of a scene with high precision in all three coordinates is key to applications ranging from LIDAR to fluorescence lifetime imaging. However, compromises that sacrifice, for example, spatial resolution at the expense of temporal resolution are often required, in particular when the full 3-dimensional data cube is required in short acquisition times. We introduce a sensor fusion approach that combines data having low-spatial resolution but high temporal precision gathered with a single-photon-avalanche-diode (SPAD) array with data that has high spatial but no temporal resolution, such as that acquired with a standard CMOS camera. Our method, based on blurring the image on the SPAD array and computational sensor fusion, reconstructs time-resolved images at significantly higher spatial resolution than the SPAD input, upsampling numerical data by a factor 12x12, and demonstrating up to 4x4 upsampling of experimental data. We demonstrate the technique for both LIDAR applications and FLIM of fluorescent cancer cells. This technique paves the way to high spatial resolution SPAD imaging or, equivalently, FLIM imaging with conventional microscopes at frame rates accelerated by more than an order of magnitude.
引用
收藏
页数:8
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