Mitigating Over-Saturated Fluorescence Images Through a Semi-Supervised Generative Adversarial Network
Year: 2024
Type: conference-paper
Abstract: Multiplex immunofluorescence (MxIF) imaging is a critical tool in biomedical research, offering detailed insights into cell composition and spatial context. As an example, DAPI staining identifies cell nuclei, while CD20 staining helps segment cell membranes in MxIF. However, a persistent challenge in MxIF is saturation artifacts, which hinder single-cell level analysis in areas with over-saturated pixels. Traditional gamma correction methods for fixing saturation are limited, often incorrectly assuming uniform distribution of saturation, which is rarely the case in practice. This paper introduces a novel approach to correct saturation artifacts from a data-driven perspective. We introduce a two-stage, high-resolution hybrid generative adversarial network (HDmixGAN), which merges unpaired (CycleGAN) and paired (pix2pixHD) network architectures. This approach is designed to capitalize on the available small-scale paired data and the more extensive unpaired data from costly MxIF data. Specifically, we generate pseudo-paired data from large-scale unpaired over-saturated datasets with a CycleGAN, and train a Pix2pixGAN using both small-scale real and large-scale synthetic data derived from multiple DAPI staining rounds in MxIF. This method was validated against various baselines in a downstream nuclei detection task, improving the F1 score by 6% over the baseline. This is, to our knowledge, the first focused effort to address multi-round saturation in MxIF images, offering a specialized solution for enhancing cell analysis accuracy through improved image quality. The source code and implementation of the proposed method are available at https://github.com/MASILab/DAPIArtifactRemoval.git.
Institutions: Vanderbilt University Medical Center, Vanderbilt University
Language: English
Topic: Image Enhancement Techniques
Subfield: Computer Vision and Pattern Recognition
Field: Computer Science
Domain: Physical Sciences
Open Access status: green
Funders: National Science Foundation, U.S. Department of Veterans Affairs, Patient-Centered Outcomes Research Institute, Vanderbilt University, Leona M. and Harry B. Helmsley Charitable Trust, Nvidia, Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Georgia Clinical and Translational Science Alliance, National Institutes of Health, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Advancing Translational Sciences
Awards: G1016015727, G1173929046, Vanderbilt Institute for Clinical and Translational Research (VICTR), G1296419534, G1331061530, G1486488711, CAREER: Modeling Personalized Brain Development with Big Data, G1853596577, G2109392540, G2284173953, Tuft cell heterogeneity in function, lineage, and structure in ileal inflammatory disease, G3002259123, NSF Convergence Accelerator Track D: Scalable, TRaceable Ai for Imaging Translation: Innovation to Implementation for Accelerated Impact (STRAIT I3), G3514670832, G3606619490, Medical Scientist Training Program, G3903728482, G3958555850, G4104170852, G4195101910, G5614773401, G5993123900, G6246474086, G6573109839, Spermidine as a New Therapy for Colitis and Chemopreventive for Colitis-associated Carcinogenesis, G6671297155, G7720434847, G7813763335, G8214155716, G872640053, G9000026873, G9000041293, G9000117310, G9000128600, G9000141600, Molecular and Cellular Basis for Digestive Diseases, G95160140
OpenAlex ID: W4401752162
