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Accurate and fast mitotic detection using an anchor-free method based on full-scale connection with recurrent deep layer aggregation in 4D microscopy images.
Kitrungrotsakul, Titinunt; Iwamoto, Yutaro; Takemoto, Satoko; Yokota, Hideo; Ipponjima, Sari; Nemoto, Tomomi; Lin, Lanfen; Tong, Ruofeng; Li, Jingsong; Chen, Yen-Wei.
Afiliação
  • Kitrungrotsakul T; Research Center for Healthcare Data Science, Zhejiang Lab, Hangzhou, China.
  • Iwamoto Y; Graduate School of Information Science and Engineering, Ritsumeikan University, Kusatsu, Shiga, Japan.
  • Takemoto S; Graduate School of Information Science and Engineering, Ritsumeikan University, Kusatsu, Shiga, Japan.
  • Yokota H; Center for Advanced Photonics, RIKEN, Wako, Saitama, Japan.
  • Ipponjima S; Center for Advanced Photonics, RIKEN, Wako, Saitama, Japan.
  • Nemoto T; Research Institute for Electronic Science, Hokkaido University, Sapporo, Hokkaido, Japan.
  • Lin L; Research Institute for Electronic Science, Hokkaido University, Sapporo, Hokkaido, Japan.
  • Tong R; College of Computer Science and Technology, Zhejiang University, Hangzhou, China.
  • Li J; Research Center for Healthcare Data Science, Zhejiang Lab, Hangzhou, China.
  • Chen YW; College of Computer Science and Technology, Zhejiang University, Hangzhou, China.
BMC Bioinformatics ; 22(1): 91, 2021 Feb 26.
Article em En | MEDLINE | ID: mdl-33637042
ABSTRACT

BACKGROUND:

To 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.

RESULTS:

In 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.

CONCLUSIONS:

Our 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Redes Neurais de Computação / Microscopia Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Redes Neurais de Computação / Microscopia Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article