Cell instance segmentation in fluorescence microscopy images is becoming essential for cancer dynamics and prognosis. Data extracted from cancer dynamics allows to understand and accurately model different metabolic processes such as proliferation. This enables customized and more precise cancer treatments. However, accurate cell instance segmentation, necessary for further cell tracking and behavior analysis, is still challenging in scenarios with high cell concentration and overlapping edges. Within this framework, we propose a novel cell instance segmentation approach based on the well-known U-Net architecture. To enforce the learning of morphological information per pixel, a deep distance transformer (DDT) acts as a back-bone model. The DDT output is subsequently used to train a top-model. The following top-models are considered: a three-class (\emph{e.g.,} foreground, background and cell border) U-net, and a watershed transform. The obtained results suggest a performance boost over traditional U-Net architectures. This opens an interesting research line around the idea of injecting morphological information into a fully convolutional model.
翻译:荧光显微镜图像中的细胞分解正在成为癌症动态和预测的关键。从癌症动态中提取的数据能够理解和准确地模拟扩散等不同代谢过程,从而能够进行定制化和更加精确的癌症治疗。然而,对于进一步细胞跟踪和行为分析而言,准确的细胞分解对于细胞集中度和相重叠边缘仍然具有挑战性。在此框架内,我们提议基于众所周知的 U-Net 结构的新颖的细胞分解方法。为了将形态信息学习到像素中,一个远距变异器(DDT)作为后骨模型。DDT 输出随后被用于培训顶级模型。以下顶级模型被考虑:三层(emph{e{e.g.) 地表、背景和细胞边框) U-net 和 流域变形。获得的结果表明传统U-Net 结构的性能增强力。这开启了围绕注射形态信息进入完全进化模型的有趣研究线。