Artifact-free whole-slide imaging with structured illumination microscopy and Bayesian image reconstruction

被引:16
作者
Johnson, Karl A. [1 ]
Hagen, Guy M. [1 ]
机构
[1] Univ Colorado, UCCS BioFrontiers Ctr, 1420 Austin Bluffs Pkwy, Colorado Springs, CO 80918 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
structured illumination microscopy; SIM; image stitching; Bayesian methods; MAP-SIM; SIMToolbox; histopathology; cancer; FLUORESCENCE MICROSCOPY; LIVE CELLS; RESOLUTION; LIGHT;
D O I
10.1093/gigascience/giaa035
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Structured illumination microscopy (SIM) is a method that can be used to image biological samples and can achieve both optical sectioning and super-resolution effects. Optimization of the imaging set-up and data-processing methods results in high-quality images without artifacts due to mosaicking or due to the use of SIM methods. Reconstruction methods based on Bayesian estimation can be used to produce images with a resolution beyond that dictated by the optical system. Five complete datasets are presented including large panoramic SIM images of human tissues in pathophysiological conditions. Cancers of the prostate, skin, ovary, and breast, as well as tuberculosis of the lung, were imaged using SIM. The samples are available commercially and are standard histological preparations stained with hematoxylin-eosin. The use of fluorescence microscopy is increasing in histopathology. There is a need for methods that reduce artifacts caused by the use of image-stitching methods or optical sectioning methods such as SIM. Stitched SIM images produce results that may be useful for intraoperative histology. Releasing high-quality, full-slide images and related data will aid researchers in furthering the field of fluorescent histopathology.
引用
收藏
页数:14
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