4.7 Article

DeepHCS plus plus : Bright-field to fluorescence microscopy image conversion using multi-task learning with adversarial losses for label-free high-content screening

期刊

MEDICAL IMAGE ANALYSIS
卷 70, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.media.2021.101995

关键词

Bright-field microscopy; Fluorescence microscopy; High-content screening; Precision medicine; Apoptosis; DAPI; Cytoplasm; Deep learning

资金

  1. Bio AMP
  2. Medical Technology Development Program of the National Research Foundation of Korea (NRF) - Ministry of Science and ICT (MSIT) [NRF-2019M3E5D2A01063819]
  3. Brain Research Program of the National Research Foundation of Korea (NRF) - Ministry of Science and ICT (MSIT) [NRF-2017M3C7A1047904]
  4. Korea Health Technology RAMP
  5. D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health AMP
  6. Welfare, Republic of Korea [HI18C0316]
  7. ICT Creative Consilience program of the Institute for Information AMP
  8. communications Technology Planning AMP
  9. Evaluation (IITP) - MSIT [IITP-2021-0-01819]
  10. National Research Foundation of Korea [4199990214667] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The proposed method in this paper aims to transform bright-field microscopy images into synthetic fluorescence images for observing cell apoptosis, nuclei, and cytoplasm, commonly used in drug screening. By leveraging deep learning and multi-task learning with adversarial losses, the proposed method generates accurate and realistic synthetic fluorescence images, reducing preparation time and improving screening efficiency.
In this paper, we propose a novel microscopy image translation method for transforming a bright-field microscopy image into three different fluorescence images to observe the apoptosis, nuclei, and cytoplasm of cells, which visualize dead cells, nuclei of cells, and cytoplasm of cells, respectively. These biomarkers are commonly used in high-content drug screening to analyze drug response. The main contribution of the proposed work is the automatic generation of three fluorescence images from a conventional bright field image; this can greatly reduce the time-consuming and laborious tissue preparation process and improve throughput of the screening process. Our proposed method uses only a single bright-field image and the corresponding fluorescence images as a set of image pairs for training an end-to-end deep convolutional neural network. By leveraging deep convolutional neural networks with a set of image pairs of bright-field and corresponding fluorescence images, our proposed method can produce synthetic fluorescence images comparable to real fluorescence microscopy images with high accuracy. Our proposed model uses multi-task learning with adversarial losses to generate more accurate and realistic microscopy images. We assess the efficacy of the proposed method using real bright-field and fluorescence microscopy image datasets from patient-driven samples of a glioblastoma, and validate the method's accuracy with various quality metrics including cell number correlation (CNC), peak signal-to-noise ratio (PSNR), structural similarity index measure (SSIM), cell viability correlation (CVC), error maps, and R 2 correlation. (c) 2021 Elsevier B.V. All rights reserved.

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