Abstract

The accurate segmentation and tracking of cells in microscopy image sequences is an important task in biomedical research, e.g., for studying the development of tissues, organs or entire organisms. However, the segmentation of touching cells in images with a low signal-to-noise-ratio is still a challenging problem. In this paper, we present a method for the segmentation of touching cells in microscopy images. By using a novel representation of cell borders, inspired by distance maps, our method is capable to utilize not only touching cells but also close cells in the training process. Furthermore, this representation is notably robust to annotation errors and shows promising results for the segmentation of microscopy images containing in the training data underrepresented or not included cell types. For the prediction of the proposed neighbor distances, an adapted U-Net convolutional neural network (CNN) with two decoder paths is used. In addition, we adapt a graph-based cell tracking algorithm to evaluate our proposed method on the task of cell tracking. The adapted tracking algorithm includes a movement estimation in the cost function to re-link tracks with missing segmentation masks over a short sequence of frames. Our combined tracking by detection method has proven its potential in the IEEE ISBI 2020 Cell Tracking Challenge (http://celltrackingchallenge.net/) where we achieved as team KIT-Sch-GE multiple top three rankings including two top performances using a single segmentation model for the diverse data sets.

Highlights

  • State-of-the-art microscopy imaging techniques such as light-sheet fluorescence microscopy imaging enable to investigate cell dynamics with single-cell resolution [1, 2]

  • The provided annotations consist of gold truth (GT) instance segmentation masks, interlinked GT cell seeds for cell detection and tracking, and computer-generated instance segmentation masks, referred to as silver truth (ST)

  • This is due to the fact that the neighbor distances enable our method to learn from close cells which results in additional information in the training process and the fact that this information can be combined with the cell distances

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Summary

Introduction

State-of-the-art microscopy imaging techniques such as light-sheet fluorescence microscopy imaging enable to investigate cell dynamics with single-cell resolution [1, 2]. This allows to study cell migration and proliferation in tissue development and organ formation at early embryonic stages. Establishing the required complete lineage of each cell, requires a virtually error-free segmentation and tracking of individual cells over time [2, 3]. A manual data analysis is unfeasible, due to the large amount of data acquired with modern imaging. Cell segmentation and tracking using CNN-based distance predictions and a graph-based matching strategy.

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