SR-CACO-2: A Dataset for Confocal Fluorescence Microscopy Image Super-Resolution

Fuente: arXiv
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Belharbi, Soufiane, Whitford, Mara KM, Hoang, Phuong, Murtaza, Shakeeb, McCaffrey, Luke, Granger, Eric
Format: Preprint
Veröffentlicht: 2024
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1866909373594337280
author Belharbi, Soufiane
Whitford, Mara KM
Hoang, Phuong
Murtaza, Shakeeb
McCaffrey, Luke
Granger, Eric
author_facet Belharbi, Soufiane
Whitford, Mara KM
Hoang, Phuong
Murtaza, Shakeeb
McCaffrey, Luke
Granger, Eric
contents Confocal fluorescence microscopy is one of the most accessible and widely used imaging techniques for the study of biological processes at the cellular and subcellular levels. Scanning confocal microscopy allows the capture of high-quality images from thick three-dimensional (3D) samples, yet suffers from well-known limitations such as photobleaching and phototoxicity of specimens caused by intense light exposure, limiting its applications. Cellular damage can be alleviated by changing imaging parameters to reduce light exposure, often at the expense of image quality. Machine/deep learning methods for single-image super-resolution (SISR) can be applied to restore image quality by upscaling lower-resolution (LR) images to yield high-resolution images (HR). These SISR methods have been successfully applied to photo-realistic images due partly to the abundance of publicly available data. In contrast, the lack of publicly available data partly limits their application and success in scanning confocal microscopy. In this paper, we introduce a large scanning confocal microscopy dataset named SR-CACO-2 that is comprised of low- and high-resolution image pairs marked for three different fluorescent markers. It allows the evaluation of performance of SISR methods on three different upscaling levels (X2, X4, X8). SR-CACO-2 contains the human epithelial cell line Caco-2 (ATCC HTB-37), and it is composed of 2,200 unique images, captured with four resolutions and three markers, forming 9,937 image patches for SISR methods. We provide benchmarking results for 16 state-of-the-art methods of the main SISR families. Results show that these methods have limited success in producing high-resolution textures. The dataset is freely accessible under a Creative Commons license (CC BY-NC-SA 4.0). Our dataset, code and pretrained weights for SISR methods are available: https://github.com/sbelharbi/sr-caco-2.
format Preprint
id arxiv_https___arxiv_org_abs_2406_09168
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle SR-CACO-2: A Dataset for Confocal Fluorescence Microscopy Image Super-Resolution
Belharbi, Soufiane
Whitford, Mara KM
Hoang, Phuong
Murtaza, Shakeeb
McCaffrey, Luke
Granger, Eric
Image and Video Processing
Computer Vision and Pattern Recognition
Machine Learning
Confocal fluorescence microscopy is one of the most accessible and widely used imaging techniques for the study of biological processes at the cellular and subcellular levels. Scanning confocal microscopy allows the capture of high-quality images from thick three-dimensional (3D) samples, yet suffers from well-known limitations such as photobleaching and phototoxicity of specimens caused by intense light exposure, limiting its applications. Cellular damage can be alleviated by changing imaging parameters to reduce light exposure, often at the expense of image quality. Machine/deep learning methods for single-image super-resolution (SISR) can be applied to restore image quality by upscaling lower-resolution (LR) images to yield high-resolution images (HR). These SISR methods have been successfully applied to photo-realistic images due partly to the abundance of publicly available data. In contrast, the lack of publicly available data partly limits their application and success in scanning confocal microscopy. In this paper, we introduce a large scanning confocal microscopy dataset named SR-CACO-2 that is comprised of low- and high-resolution image pairs marked for three different fluorescent markers. It allows the evaluation of performance of SISR methods on three different upscaling levels (X2, X4, X8). SR-CACO-2 contains the human epithelial cell line Caco-2 (ATCC HTB-37), and it is composed of 2,200 unique images, captured with four resolutions and three markers, forming 9,937 image patches for SISR methods. We provide benchmarking results for 16 state-of-the-art methods of the main SISR families. Results show that these methods have limited success in producing high-resolution textures. The dataset is freely accessible under a Creative Commons license (CC BY-NC-SA 4.0). Our dataset, code and pretrained weights for SISR methods are available: https://github.com/sbelharbi/sr-caco-2.
title SR-CACO-2: A Dataset for Confocal Fluorescence Microscopy Image Super-Resolution
topic Image and Video Processing
Computer Vision and Pattern Recognition
Machine Learning
url https://arxiv.org/abs/2406.09168