University of Texas Southwestern Medical Center, Department of Clinical Science, Dallas, Texas, United States.
Daegu Gyeongbuk Institute of Science and Technology, Department of Robotics Engineering, Dalseong-gu, Republic of Korea.
J Biomed Opt. 2021 Mar;26(3). doi: 10.1117/1.JBO.26.3.036001.
Digital holographic microscopy (DHM) is a promising technique for the study of semitransparent biological specimen such as red blood cells (RBCs). It is important and meaningful to detect and count biological cells at the single cell level in biomedical images for biomarker discovery and disease diagnostics. However, the biological cell analysis based on phase information of images is inefficient due to the complexity of numerical phase reconstruction algorithm applied to raw hologram images. New cell study methods based on diffraction pattern directly are desirable.
Deep fully convolutional networks (FCNs) were developed on raw hologram images directly for high-throughput label-free cell detection and counting to assist the biological cell analysis in the future.
The raw diffraction patterns of RBCs were recorded by use of DHM. Ground-truth mask images were labeled based on phase images reconstructed from RBC holograms using numerical reconstruction algorithm. A deep FCN, which is UNet, was trained on the diffraction pattern images to achieve the label-free cell detection and counting.
The implemented deep FCNs provide a promising way to high-throughput and label-free counting of RBCs with a counting accuracy of 99% at a throughput rate of greater than 288 cells per second and 200 μm × 200 μm field of view at the single cell level. Compared to convolutional neural networks, the FCNs can get much better results in terms of accuracy and throughput rate.
High-throughput label-free cell detection and counting were successfully achieved from diffraction patterns with deep FCNs. It is a promising approach for biological specimen analysis based on raw hologram directly.
数字全息显微镜 (DHM) 是研究半透明生物标本(如红细胞 (RBC))的有前途的技术。在生物医学图像中以单细胞水平检测和计数生物细胞对于发现生物标志物和疾病诊断非常重要且有意义。然而,由于应用于原始全息图的数值相位重建算法的复杂性,基于图像相位信息的生物细胞分析效率低下。需要新的基于直接衍射模式的细胞研究方法。
直接在原始全息图上开发深度全卷积网络 (FCN),用于高通量无标记细胞检测和计数,以协助未来的生物细胞分析。
使用 DHM 记录 RBC 的原始衍射图案。根据使用数值重建算法从 RBC 全息图重建的相位图像,对基于地面实况掩模图像进行标记。深度 FCN(即 UNet)在衍射模式图像上进行训练,以实现无标记细胞检测和计数。
所实现的深度 FCN 为高通量和无标记 RBC 计数提供了一种有前途的方法,在单细胞水平的 200 μm × 200 μm 视场和大于 288 个细胞/秒的吞吐量下,计数精度达到 99%。与卷积神经网络相比,FCN 在准确性和吞吐量方面可以获得更好的结果。
成功地从深度 FCN 的衍射模式实现了高通量无标记细胞检测和计数。这是一种基于原始全息图直接进行生物标本分析的有前途的方法。