首页> 美国卫生研究院文献>other >Uncertainty Footprint: Visualization of Nonuniform Behavior of Iterative Algorithms Applied to 4D Cell Tracking
【2h】

Uncertainty Footprint: Visualization of Nonuniform Behavior of Iterative Algorithms Applied to 4D Cell Tracking

机译:不确定足迹:应用于4D单元跟踪的迭代算法的非均匀行为的可视化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Research on microscopy data from developing biological samples usually requires tracking individual cells over time. When cells are three-dimensionally and densely packed in a time-dependent scan of volumes, tracking results can become unreliable and uncertain. Not only are cell segmentation results often inaccurate to start with, but it also lacks a simple method to evaluate the tracking outcome. Previous cell tracking methods have been validated against benchmark data from real scans or artificial data, whose ground truth results are established by manual work or simulation. However, the wide variety of real-world data makes an exhaustive validation impossible. Established cell tracking tools often fail on new data, whose issues are also difficult to diagnose with only manual examinations. Therefore, data-independent tracking evaluation methods are desired for an explosion of microscopy data with increasing scale and resolution. In this paper, we propose the uncertainty footprint, an uncertainty quantification and visualization technique that examines nonuniformity at local convergence for an iterative evaluation process on a spatial domain supported by partially overlapping bases. We demonstrate that the patterns revealed by the uncertainty footprint indicate data processing quality in two algorithms from a typical cell tracking workflow – cell identification and association. A detailed analysis of the patterns further allows us to diagnose issues and design methods for improvements. A 4D cell tracking workflow equipped with the uncertainty footprint is capable of self diagnosis and correction for a higher accuracy than previous methods whose evaluation is limited by manual examinations.
机译:对来自发育中的生物样品的显微镜数据进行研究通常需要随时间跟踪单个细胞。如果在与时间相关的体积扫描中将细胞三维地密集排列,则跟踪结果可能变得不可靠且不确定。不仅细胞分割结果开始时通常不准确,而且缺乏评估跟踪结果的简单方法。先前的细胞跟踪方法已经针对来自真实扫描或人工数据的基准数据进行了验证,这些数据的真实性结果是通过人工或仿真确定的。但是,现实世界中的各种数据使得无法进行详尽的验证。既定的单元跟踪工具通常无法处理新数据,仅通过手动检查也难以诊断其问题。因此,需要与数据无关的跟踪评估方法,以用于随着规模和分辨率的增加而爆炸的显微镜数据。在本文中,我们提出了不确定性足迹,一种不确定性量化和可视化技术,该技术检查局部收敛时的不均匀性,以便在部分重叠的基础支持的空间域上进行迭代评估。我们证明了不确定足迹所揭示的模式通过典型的细胞跟踪工作流程中的两种算法(细胞识别和关联)表明了数据处理质量。对模式的详细分析进一步使我们能够诊断问题并设计改进方法。配备有不确定性足迹的4D单元跟踪工作流能够进行自我诊断和校正,其准确性要高于以前的方法(其方法受到手动检查的限制)。

著录项

  • 期刊名称 other
  • 作者

    Y. Wan; C. Hansen;

  • 作者单位
  • 年(卷),期 -1(36),3
  • 年度 -1
  • 页码 479–489
  • 总页数 24
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号