TY - JOUR
T1 - Digital staining through the application of deep neural networks to multi-modal multi-photon microscopy
AU - Borhani, Navid
AU - Bower, Andrew J.
AU - Boppart, Stephen A.
AU - Psaltis, Demetri
N1 - Funding Information:
U.S. National Institutes of Health (R01 EB023232 and R01 EB013723); the U.S. National Science Foundation (CBET 18-41539).
Publisher Copyright:
© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Deep neural networks have been used to map multi-modal, multi-photon microscopy measurements of a label-free tissue sample to its corresponding histologically stained brightfield microscope colour image. It is shown that the extra structural and functional contrasts provided by using two source modes, namely two-photon excitation microscopy and fluorescence lifetime imaging, result in a more faithful reconstruction of the target haematoxylin and eosin stained mode. This modal mapping procedure can aid histopathologists, since it provides access to unobserved imaging modalities, and translates the high-dimensional numerical data generated by multi-modal, multi-photon microscopy into traditionally accepted visual forms. Furthermore, by combining the strengths of traditional chemical staining and modern multi-photon microscopy techniques, modal mapping enables label-free, non-invasive studies of in vivo tissue samples or intravital microscopic imaging inside living animals. The results show that modal co-registration and the inclusion of spatial variations increase the visual accuracy of the mapped results.
AB - Deep neural networks have been used to map multi-modal, multi-photon microscopy measurements of a label-free tissue sample to its corresponding histologically stained brightfield microscope colour image. It is shown that the extra structural and functional contrasts provided by using two source modes, namely two-photon excitation microscopy and fluorescence lifetime imaging, result in a more faithful reconstruction of the target haematoxylin and eosin stained mode. This modal mapping procedure can aid histopathologists, since it provides access to unobserved imaging modalities, and translates the high-dimensional numerical data generated by multi-modal, multi-photon microscopy into traditionally accepted visual forms. Furthermore, by combining the strengths of traditional chemical staining and modern multi-photon microscopy techniques, modal mapping enables label-free, non-invasive studies of in vivo tissue samples or intravital microscopic imaging inside living animals. The results show that modal co-registration and the inclusion of spatial variations increase the visual accuracy of the mapped results.
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U2 - 10.1364/BOE.10.001339
DO - 10.1364/BOE.10.001339
M3 - Article
C2 - 30891350
AN - SCOPUS:85063935319
SN - 2156-7085
VL - 10
SP - 1339
EP - 1350
JO - Biomedical Optics Express
JF - Biomedical Optics Express
IS - 3
M1 - 355205
ER -