A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations

The automatic detection of cells in microscopy image sequences is a significant task in biomedical research. However, routine microscopy images with cells, which are taken during the process whereby constant division and differentiation occur, are notoriously difficult to detect due to changes in th...

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Main Authors: Hao Wu, Jovial Niyogisubizo, Keliang Zhao, Jintao Meng, Wenhui Xi, Hongchang Li, Yi Pan, Yanjie Wei
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/22/16028
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author Hao Wu
Jovial Niyogisubizo
Keliang Zhao
Jintao Meng
Wenhui Xi
Hongchang Li
Yi Pan
Yanjie Wei
author_facet Hao Wu
Jovial Niyogisubizo
Keliang Zhao
Jintao Meng
Wenhui Xi
Hongchang Li
Yi Pan
Yanjie Wei
author_sort Hao Wu
collection DOAJ
description The automatic detection of cells in microscopy image sequences is a significant task in biomedical research. However, routine microscopy images with cells, which are taken during the process whereby constant division and differentiation occur, are notoriously difficult to detect due to changes in their appearance and number. Recently, convolutional neural network (CNN)-based methods have made significant progress in cell detection and tracking. However, these approaches require many manually annotated data for fully supervised training, which is time-consuming and often requires professional researchers. To alleviate such tiresome and labor-intensive costs, we propose a novel weakly supervised learning cell detection and tracking framework that trains the deep neural network using incomplete initial labels. Our approach uses incomplete cell markers obtained from fluorescent images for initial training on the Induced Pluripotent Stem (iPS) cell dataset, which is rarely studied for cell detection and tracking. During training, the incomplete initial labels were updated iteratively by combining detection and tracking results to obtain a model with better robustness. Our method was evaluated using two fields of the iPS cell dataset, along with the cell detection accuracy (DET) evaluation metric from the Cell Tracking Challenge (CTC) initiative, and it achieved 0.862 and 0.924 DET, respectively. The transferability of the developed model was tested using the public dataset FluoN2DH-GOWT1, which was taken from CTC; this contains two datasets with reference annotations. We randomly removed parts of the annotations in each labeled data to simulate the initial annotations on the public dataset. After training the model on the two datasets, with labels that comprise 10% cell markers, the DET improved from 0.130 to 0.903 and 0.116 to 0.877. When trained with labels that comprise 60% cell markers, the performance was better than the model trained using the supervised learning method. This outcome indicates that the model’s performance improved as the quality of the labels used for training increased.
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spelling doaj.art-1d3b8d4966ea4addbc9fdc73335ac7962023-11-24T14:45:36ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-11-0124221602810.3390/ijms242216028A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial AnnotationsHao Wu0Jovial Niyogisubizo1Keliang Zhao2Jintao Meng3Wenhui Xi4Hongchang Li5Yi Pan6Yanjie Wei7Shenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaShenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaShenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaShenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaShenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaInstitute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaCollege of Computer Science and Control Engineering, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaShenzhen Key Laboratory of Intelligent Bioinformatics and Center for High Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, ChinaThe automatic detection of cells in microscopy image sequences is a significant task in biomedical research. However, routine microscopy images with cells, which are taken during the process whereby constant division and differentiation occur, are notoriously difficult to detect due to changes in their appearance and number. Recently, convolutional neural network (CNN)-based methods have made significant progress in cell detection and tracking. However, these approaches require many manually annotated data for fully supervised training, which is time-consuming and often requires professional researchers. To alleviate such tiresome and labor-intensive costs, we propose a novel weakly supervised learning cell detection and tracking framework that trains the deep neural network using incomplete initial labels. Our approach uses incomplete cell markers obtained from fluorescent images for initial training on the Induced Pluripotent Stem (iPS) cell dataset, which is rarely studied for cell detection and tracking. During training, the incomplete initial labels were updated iteratively by combining detection and tracking results to obtain a model with better robustness. Our method was evaluated using two fields of the iPS cell dataset, along with the cell detection accuracy (DET) evaluation metric from the Cell Tracking Challenge (CTC) initiative, and it achieved 0.862 and 0.924 DET, respectively. The transferability of the developed model was tested using the public dataset FluoN2DH-GOWT1, which was taken from CTC; this contains two datasets with reference annotations. We randomly removed parts of the annotations in each labeled data to simulate the initial annotations on the public dataset. After training the model on the two datasets, with labels that comprise 10% cell markers, the DET improved from 0.130 to 0.903 and 0.116 to 0.877. When trained with labels that comprise 60% cell markers, the performance was better than the model trained using the supervised learning method. This outcome indicates that the model’s performance improved as the quality of the labels used for training increased.https://www.mdpi.com/1422-0067/24/22/16028cell detectioncell trackingdeep learningweakly supervised learningiPS cell reprogrammingbrightfield microscopy
spellingShingle Hao Wu
Jovial Niyogisubizo
Keliang Zhao
Jintao Meng
Wenhui Xi
Hongchang Li
Yi Pan
Yanjie Wei
A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
International Journal of Molecular Sciences
cell detection
cell tracking
deep learning
weakly supervised learning
iPS cell reprogramming
brightfield microscopy
title A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
title_full A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
title_fullStr A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
title_full_unstemmed A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
title_short A Weakly Supervised Learning Method for Cell Detection and Tracking Using Incomplete Initial Annotations
title_sort weakly supervised learning method for cell detection and tracking using incomplete initial annotations
topic cell detection
cell tracking
deep learning
weakly supervised learning
iPS cell reprogramming
brightfield microscopy
url https://www.mdpi.com/1422-0067/24/22/16028
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