arXivDaily arXiv每日学术速递 周一至周五更新
arXiv 1705.03386cs.CV
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通过建议生成和选择的单元格跟踪

Cell Tracking via Proposal Generation and Selection

University of Oulu(奥卢大学);Aalto University(阿尔托大学)

Saad Ullah Akram, Juho Kannala, Lauri Eklund, Janne Heikkilä

摘要:

显微成像在理解发育和疾病中的许多生物过程中起着至关重要的作用。显微镜自动化和活细胞成像方法和标记物的开发的最新进展导致捕获的图像数据量快速增长。为了有效和可靠地从这些捕获的序列中提取有用的见解,自动化细胞跟踪至关重要。这是一个具有挑战性的问题,由于在外观和形状的细胞取决于许多因素,包括成像方法,细胞的生物学特性,细胞基质组成,标记方法等,通常细胞跟踪方法需要一个序列特异性的分割方法和手动调整许多跟踪参数,这限制了它们的适用性序列以外的其他设计。在本文中,我们提出了1)一种基于深度学习的细胞提议方法,该方法提出了细胞候选及其分数,以及2)一种细胞跟踪方法,该方法使用表示不同细胞事件的边缘在图形模型中链接相邻帧中的提议,并将联合细胞检测和跟踪作为对细胞和边缘提议子集的选择。我们的方法是完全自动化的,并给予足够的训练数据,可以应用于各种各样的显微镜序列。我们评估我们的方法在多个荧光和相差显微镜序列包含各种形状和外观的细胞从ISBI细胞跟踪挑战,并表明我们的方法优于现有的细胞跟踪方法。代码可在:https://github.com/SaadUllahAkram/CellTracker

英文摘要:

Microscopy imaging plays a vital role in understanding many biological processes in development and disease. The recent advances in automation of microscopes and development of methods and markers for live cell imaging has led to rapid growth in the amount of image data being captured. To efficiently and reliably extract useful insights from these captured sequences, automated cell tracking is essential. This is a challenging problem due to large variation in the appearance and shapes of cells depending on many factors including imaging methodology, biological characteristics of cells, cell matrix composition, labeling methodology, etc. Often cell tracking methods require a sequence-specific segmentation method and manual tuning of many tracking parameters, which limits their applicability to sequences other than those they are designed for. In this paper, we propose 1) a deep learning based cell proposal method, which proposes candidates for cells along with their scores, and 2) a cell tracking method, which links proposals in adjacent frames in a graphical model using edges representing different cellular events and poses joint cell detection and tracking as the selection of a subset of cell and edge proposals. Our method is completely automated and given enough training data can be applied to a wide variety of microscopy sequences. We evaluate our method on multiple fluorescence and phase contrast microscopy sequences containing cells of various shapes and appearances from ISBI cell tracking challenge, and show that our method outperforms existing cell tracking methods. Code is available at: https://github.com/SaadUllahAkram/CellTracker

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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