一种二维荧光显微镜图像序列中细胞核自动跟踪的方法

Alexandr Yu. Kondrati'ev, H. Yaginuma, Y. Okada, D. Sorokin
{"title":"一种二维荧光显微镜图像序列中细胞核自动跟踪的方法","authors":"Alexandr Yu. Kondrati'ev, H. Yaginuma, Y. Okada, D. Sorokin","doi":"10.1109/IPTA.2018.8608156","DOIUrl":null,"url":null,"abstract":"The automated segmentation and tracking of cells in live cell microscopy image sequences is an actual problem in many biological research areas. Despite the existence of different cell tracking approaches, a universal solution for this problem still does not exist due to high variety of fluorescent microscopy image data obtained using different techniques, where cells have completely different visual appearance. Moreover, the cells can significantly change their shape even within a single image sequence. In this work, we propose a cell tracking algorithm designed for detecting and tracking cell nuclei in 2D image sequences obtained by epifluorescence microscopy, where the cell appearance drastically changes during cell mitosis. We used marker controlled watershed algorithm combined with blob detection for nuclei segmentation followed by a generalized nearest neighbor approach for nuclei tracking. We also employed a special mitosis detection algorithm to process cell division events. Our approach was quantitatively evaluated for its segmentation and tracking accuracy using the real image data annotated by human experts. The evaluation procedure was performed based on the protocol used in the Cell Tracking Challenge. It was shown that the proposed approach outperforms an existing semiautomatic method in both segmentation and tracking accuracy.","PeriodicalId":272294,"journal":{"name":"2018 Eighth International Conference on Image Processing Theory, Tools and Applications (IPTA)","volume":"11 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"A Method for Automatic Tracking of Cell Nuclei in 2D Epifluorescence Microscopy Image Sequences\",\"authors\":\"Alexandr Yu. Kondrati'ev, H. Yaginuma, Y. Okada, D. Sorokin\",\"doi\":\"10.1109/IPTA.2018.8608156\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The automated segmentation and tracking of cells in live cell microscopy image sequences is an actual problem in many biological research areas. Despite the existence of different cell tracking approaches, a universal solution for this problem still does not exist due to high variety of fluorescent microscopy image data obtained using different techniques, where cells have completely different visual appearance. Moreover, the cells can significantly change their shape even within a single image sequence. In this work, we propose a cell tracking algorithm designed for detecting and tracking cell nuclei in 2D image sequences obtained by epifluorescence microscopy, where the cell appearance drastically changes during cell mitosis. We used marker controlled watershed algorithm combined with blob detection for nuclei segmentation followed by a generalized nearest neighbor approach for nuclei tracking. We also employed a special mitosis detection algorithm to process cell division events. Our approach was quantitatively evaluated for its segmentation and tracking accuracy using the real image data annotated by human experts. The evaluation procedure was performed based on the protocol used in the Cell Tracking Challenge. It was shown that the proposed approach outperforms an existing semiautomatic method in both segmentation and tracking accuracy.\",\"PeriodicalId\":272294,\"journal\":{\"name\":\"2018 Eighth International Conference on Image Processing Theory, Tools and Applications (IPTA)\",\"volume\":\"11 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2018 Eighth International Conference on Image Processing Theory, Tools and Applications (IPTA)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/IPTA.2018.8608156\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2018 Eighth International Conference on Image Processing Theory, Tools and Applications (IPTA)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/IPTA.2018.8608156","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

活细胞显微镜图像序列中细胞的自动分割和跟踪是许多生物学研究领域的实际问题。尽管存在不同的细胞跟踪方法,但由于使用不同技术获得的荧光显微镜图像数据种类繁多,细胞具有完全不同的视觉外观,因此仍然不存在针对该问题的通用解决方案。此外,即使在单个图像序列中,细胞也可以显着改变其形状。在这项工作中,我们提出了一种细胞跟踪算法,用于检测和跟踪通过荧光显微镜获得的二维图像序列中的细胞核,其中细胞外观在细胞有丝分裂期间发生了巨大变化。我们采用标记控制分水岭算法结合blob检测进行细胞核分割,然后采用广义最近邻方法进行细胞核跟踪。我们还采用了一种特殊的有丝分裂检测算法来处理细胞分裂事件。我们的方法使用人类专家注释的真实图像数据对其分割和跟踪精度进行了定量评估。评估程序根据细胞追踪挑战中使用的协议进行。结果表明,该方法在分割和跟踪精度上都优于现有的半自动方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Method for Automatic Tracking of Cell Nuclei in 2D Epifluorescence Microscopy Image Sequences
The automated segmentation and tracking of cells in live cell microscopy image sequences is an actual problem in many biological research areas. Despite the existence of different cell tracking approaches, a universal solution for this problem still does not exist due to high variety of fluorescent microscopy image data obtained using different techniques, where cells have completely different visual appearance. Moreover, the cells can significantly change their shape even within a single image sequence. In this work, we propose a cell tracking algorithm designed for detecting and tracking cell nuclei in 2D image sequences obtained by epifluorescence microscopy, where the cell appearance drastically changes during cell mitosis. We used marker controlled watershed algorithm combined with blob detection for nuclei segmentation followed by a generalized nearest neighbor approach for nuclei tracking. We also employed a special mitosis detection algorithm to process cell division events. Our approach was quantitatively evaluated for its segmentation and tracking accuracy using the real image data annotated by human experts. The evaluation procedure was performed based on the protocol used in the Cell Tracking Challenge. It was shown that the proposed approach outperforms an existing semiautomatic method in both segmentation and tracking accuracy.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信