Research Center for Healthcare Data Science, Zhejiang Lab, Hangzhou, China.
Graduate School of Information Science and Engineering, Ritsumeikan University, Kusatsu, Shiga, Japan.
BMC Bioinformatics. 2021 Feb 26;22(1):91. doi: 10.1186/s12859-021-04014-w.
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.
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.
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.
为了有效地检测和研究各种与细胞相关的疾病,了解细胞行为至关重要。检测有丝分裂细胞的能力是诊断细胞相关疾病的基本步骤。卷积神经网络(CNN)已成功应用于目标检测任务,但在应用于有丝分裂细胞检测时,由于正常细胞与有丝分裂细胞之间存在复杂的特征差异,大多数现有方法会产生较高的假阳性率。在 2D 方法中,每个阶段的细胞大小和方向变化使得检测有丝分裂细胞变得困难。因此,有效地从有丝分裂数据中提取空间和时间特征是一项重要且具有挑战性的任务。在 4D 显微镜图像中进行有丝分裂检测的另一个主要问题是检测所需的计算时间。
在本文中,我们提出了一种名为全尺度连接递归深层聚合(RDLA++)的骨干特征提取网络,用于无锚点的有丝分裂检测。我们利用一种 2.5D 方法,该方法包括从相邻切片的几个 2D 图像中提取的 3D 空间信息,形成多流输入。
与其他最先进的方法相比,我们提出的技术解决了尺度变化问题,能够有效地从 4D 显微镜图像中提取空间和时间特征,从而提高检测精度并减少计算时间。