The Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory University, Atlanta, GA, USA.
Department of Pediatrics, Division of Pediatric Hematology/Oncology, Aflac Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
Nat Commun. 2023 Aug 18;14(1):5022. doi: 10.1038/s41467-023-40522-4.
While microscopy-based cellular assays, including microfluidics, have significantly advanced over the last several decades, there has not been concurrent development of widely-accessible techniques to analyze time-dependent microscopy data incorporating phenomena such as fluid flow and dynamic cell adhesion. As such, experimentalists typically rely on error-prone and time-consuming manual analysis, resulting in lost resolution and missed opportunities for innovative metrics. We present a user-adaptable toolkit packaged into the open-source, standalone Interactive Cellular assay Labeled Observation and Tracking Software (iCLOTS). We benchmark cell adhesion, single-cell tracking, velocity profile, and multiscale microfluidic-centric applications with blood samples, the prototypical biofluid specimen. Moreover, machine learning algorithms characterize previously imperceptible data groupings from numerical outputs. Free to download/use, iCLOTS addresses a need for a field stymied by a lack of analytical tools for innovative, physiologically-relevant assays of any design, democratizing use of well-validated algorithms for all end-user biomedical researchers who would benefit from advanced computational methods.
尽管基于显微镜的细胞分析方法(包括微流控技术)在过去几十年中取得了显著进展,但在分析涉及流体流动和动态细胞黏附等现象的依赖时间的显微镜数据方面,还没有同时开发出广泛可用的技术。因此,实验人员通常依赖容易出错且耗时的手动分析,导致分辨率降低,错失创新指标的机会。我们提出了一个用户自适应工具包,将其打包到开源独立的交互式细胞分析标记观测和跟踪软件(iCLOTS)中。我们使用血液样本(典型的生物流体样本)对细胞黏附、单细胞跟踪、速度分布和多尺度微流控中心应用进行基准测试。此外,机器学习算法从数值输出中描述以前无法察觉的数据分组。iCLOTS 免费下载/使用,解决了一个领域的需求,该领域因缺乏创新的、与生理相关的任何设计的分析工具而受到阻碍,为所有受益于先进计算方法的生物医学研究的最终用户提供了经过良好验证的算法的民主化使用。