Rapid 3D imaging at cellular resolution for digital cytopathology with a multi-camera array scanner (MCAS)

Fuente: arXiv
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Hauptverfasser: Kim, Kanghyun, Chaware, Amey, Cook, Clare B., Xu, Shiqi, Abdelmalak, Monica, Cooke, Colin, Zhou, Kevin C., Harfouche, Mark, Reamey, Paul, Saliu, Veton, Doman, Jed, Dugo, Clay, Horstmeyer, Gregor, Davis, Richard, Taylor-Cho, Ian, Foo, Wen-Chi, Kreiss, Lucas, Jiang, Xiaoyin Sara, Horstmeyer, Roarke
Format: Preprint
Veröffentlicht: 2024
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author Kim, Kanghyun
Chaware, Amey
Cook, Clare B.
Xu, Shiqi
Abdelmalak, Monica
Cooke, Colin
Zhou, Kevin C.
Harfouche, Mark
Reamey, Paul
Saliu, Veton
Doman, Jed
Dugo, Clay
Horstmeyer, Gregor
Davis, Richard
Taylor-Cho, Ian
Foo, Wen-Chi
Kreiss, Lucas
Jiang, Xiaoyin Sara
Horstmeyer, Roarke
author_facet Kim, Kanghyun
Chaware, Amey
Cook, Clare B.
Xu, Shiqi
Abdelmalak, Monica
Cooke, Colin
Zhou, Kevin C.
Harfouche, Mark
Reamey, Paul
Saliu, Veton
Doman, Jed
Dugo, Clay
Horstmeyer, Gregor
Davis, Richard
Taylor-Cho, Ian
Foo, Wen-Chi
Kreiss, Lucas
Jiang, Xiaoyin Sara
Horstmeyer, Roarke
contents Optical microscopy has long been the standard method for diagnosis in cytopathology. Whole slide scanners can image and digitize large sample areas automatically, but are slow, expensive and therefore not widely available. Clinical diagnosis of cytology specimens is especially challenging since these samples are both spread over large areas and thick, which requires 3D capture. Here, we introduce a new parallelized microscope for scanning thick specimens across extremely wide fields-of-view (54x72 mm^2) at 1.2 and 0.6 μm resolutions, accompanied by machine learning software to rapidly assess these 16 gigapixel scans. This Multi-Camera Array Scanner (MCAS) comprises 48 micro-cameras closely arranged to simultaneously image different areas. By capturing 624 megapixels per snapshot, the MCAS is significantly faster than most conventional whole slide scanners. We used this system to digitize entire cytology samples (scanning three entire slides in 3D in just several minutes) and demonstrate two machine learning techniques to assist pathologists: first, an adenocarcinoma detection model in lung specimens (0.73 recall); second, a slide-level classification model of lung smears (0.969 AUC).
format Preprint
id arxiv_https___arxiv_org_abs_2409_15722
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Rapid 3D imaging at cellular resolution for digital cytopathology with a multi-camera array scanner (MCAS)
Kim, Kanghyun
Chaware, Amey
Cook, Clare B.
Xu, Shiqi
Abdelmalak, Monica
Cooke, Colin
Zhou, Kevin C.
Harfouche, Mark
Reamey, Paul
Saliu, Veton
Doman, Jed
Dugo, Clay
Horstmeyer, Gregor
Davis, Richard
Taylor-Cho, Ian
Foo, Wen-Chi
Kreiss, Lucas
Jiang, Xiaoyin Sara
Horstmeyer, Roarke
Optics
Optical microscopy has long been the standard method for diagnosis in cytopathology. Whole slide scanners can image and digitize large sample areas automatically, but are slow, expensive and therefore not widely available. Clinical diagnosis of cytology specimens is especially challenging since these samples are both spread over large areas and thick, which requires 3D capture. Here, we introduce a new parallelized microscope for scanning thick specimens across extremely wide fields-of-view (54x72 mm^2) at 1.2 and 0.6 μm resolutions, accompanied by machine learning software to rapidly assess these 16 gigapixel scans. This Multi-Camera Array Scanner (MCAS) comprises 48 micro-cameras closely arranged to simultaneously image different areas. By capturing 624 megapixels per snapshot, the MCAS is significantly faster than most conventional whole slide scanners. We used this system to digitize entire cytology samples (scanning three entire slides in 3D in just several minutes) and demonstrate two machine learning techniques to assist pathologists: first, an adenocarcinoma detection model in lung specimens (0.73 recall); second, a slide-level classification model of lung smears (0.969 AUC).
title Rapid 3D imaging at cellular resolution for digital cytopathology with a multi-camera array scanner (MCAS)
topic Optics
url https://arxiv.org/abs/2409.15722