GE Global Research, One Research Circle, Niskayuna, 12309, NY, USA.
GE Healthcare, 1040 12th Ave NW, Issaquah, 98027, WA, USA.
BMC Bioinformatics. 2018 Oct 3;19(1):365. doi: 10.1186/s12859-018-2375-z.
Automatic and reliable characterization of cells in cell cultures is key to several applications such as cancer research and drug discovery. Given the recent advances in light microscopy and the need for accurate and high-throughput analysis of cells, automated algorithms have been developed for segmenting and analyzing the cells in microscopy images. Nevertheless, accurate, generic and robust whole-cell segmentation is still a persisting need to precisely quantify its morphological properties, phenotypes and sub-cellular dynamics.
We present a single-channel whole cell segmentation algorithm. We use markers that stain the whole cell, but with less staining in the nucleus, and without using a separate nuclear stain. We show the utility of our approach in microscopy images of cell cultures in a wide variety of conditions. Our algorithm uses a deep learning approach to learn and predict locations of the cells and their nuclei, and combines that with thresholding and watershed-based segmentation. We trained and validated our approach using different sets of images, containing cells stained with various markers and imaged at different magnifications. Our approach achieved a 86% similarity to ground truth segmentation when identifying and separating cells.
The proposed algorithm is able to automatically segment cells from single channel images using a variety of markers and magnifications.
自动且可靠地对细胞培养物中的细胞进行特征描述是癌症研究和药物发现等多个应用的关键。鉴于近年来在光学显微镜方面的进展,以及对细胞进行准确和高通量分析的需求,已经开发出用于分割和分析显微镜图像中细胞的自动化算法。然而,精确地量化其形态特征、表型和亚细胞动力学仍然需要精确、通用和稳健的全细胞分割。
我们提出了一种单通道全细胞分割算法。我们使用标记物对整个细胞进行染色,但细胞核的染色较少,并且不使用单独的核染色剂。我们在各种条件下的细胞培养物显微镜图像中展示了我们方法的实用性。我们的算法使用深度学习方法来学习和预测细胞及其细胞核的位置,并将其与阈值和基于分水岭的分割相结合。我们使用不同的图像集进行了训练和验证,其中包含用各种标记物染色并在不同放大倍数下成像的细胞。当识别和分离细胞时,我们的方法达到了与地面实况分割 86%的相似度。
该算法能够使用各种标记物和放大倍数自动从单通道图像中分割细胞。