Abstract

BackgroundTo effectively detect and investigate various cell-related diseases, it is essential to understand cell behaviour. The ability to detection mitotic cells is a fundamental step in diagnosing cell-related diseases. Convolutional neural networks (CNNs) have been successfully applied to object detection tasks, however, when applied to mitotic cell detection, most existing methods generate high false-positive rates due to the complex characteristics that differentiate normal cells from mitotic cells. Cell size and orientation variations in each stage make detecting mitotic cells difficult in 2D approaches. Therefore, effective extraction of the spatial and temporal features from mitotic data is an important and challenging task. The computational time required for detection is another major concern for mitotic detection in 4D microscopic images.ResultsIn this paper, we propose a backbone feature extraction network named full scale connected recurrent deep layer aggregation (RDLA++) for anchor-free mitotic detection. We utilize a 2.5D method that includes 3D spatial information extracted from several 2D images from neighbouring slices that form a multi-stream input.ConclusionsOur proposed technique addresses the scale variation problem and can efficiently extract spatial and temporal features from 4D microscopic images, resulting in improved detection accuracy and reduced computation time compared with those of other state-of-the-art methods.

Highlights

  • To effectively detect and investigate various cell-related diseases, it is essential to understand cell behaviour

  • Experimental setup Dataset we evaluate the performance of various mitotic detection approaches on 4D microscopic images (Japan Society for Precision Engineering, Technical Committee on Industrial Application of Image Processing Appearance inspection algorithm contest 2017 (TC-IAIP A-IA2017) [34]) using a total of 16 datasets

  • The mitotic cell stages were not provided; binary classification and detection were performed in this work

Read more

Summary

Introduction

To effectively detect and investigate various cell-related diseases, it is essential to understand cell behaviour. Effective extraction of the spatial and temporal features from mitotic data is an important and challenging task. The computational time required for detection is another major concern for mitotic detection in 4D microscopic images. The conventional techniques for detecting and counting mitotic cells are performed manually by specialists. Mitotic cells are detected and counted by observing a sample preserved between glass slides under a microscope [2,3,4]. Various methods have been proposed to solve mitotic cell detection problems [5, 6], a cell may freely perform mitosis in any orientation. Capturing mitotic cells in 2D images may lead to a loss of spatial features due to different cell orientations

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.