Matthias Pesch

Johannes Seiffarth, Keitaro Kasahara, Michelle Bund et al.

Live-cell imaging (LCI) technology enables the detailed spatio-temporal characterization of living cells at the single-cell level, which is critical for advancing research in the life sciences, from biomedical applications to bioprocessing. High-throughput setups with tens to hundreds of parallel cell cultivations offer the potential for robust and reproducible insights. However, these insights are obscured by the large amount of LCI data recorded per experiment. Recent advances in state-of-the-art deep learning methods for cell segmentation and tracking now enable the automated analysis of such large data volumes, offering unprecedented opportunities to systematically study single-cell dynamics. The next key challenge lies in integrating these powerful tools into accessible, flexible, and user-friendly workflows that support routine application in biological research. In this work, we present acia-workflows, a platform that combines three key components: (1) the Automated live-Cell Imaging Analysis (acia) Python library, which supports the modular design of image analysis pipelines offering eight deep learning segmentation and tracking approaches; (2) workflows that assemble the image analysis pipeline, its software dependencies, documentation, and visualizations into a single Jupyter Notebook, leading to accessible, reproducible and scalable analysis workflows; and (3) a collection of application workflows showcasing the analysis and customization capabilities in real-world applications. Specifically, we present three workflows to investigate various types of microfluidic LCI experiments ranging from growth rate comparisons to precise, minute-resolution quantitative analyses of individual dynamic cells responses to changing oxygen conditions. Our collection of more than ten application workflows is open source and publicly available at https://github.com/JuBiotech/acia-workflows.

Nils Friederich, Angelo Jovin Yamachui Sitcheu, Annika Nassal et al.

Microfluidic Live-Cell Imaging (MLCI) generates high-quality data that allows biotechnologists to study cellular growth dynamics in detail. However, obtaining these continuous data over extended periods is challenging, particularly in achieving accurate and consistent real-time event classification at the intersection of imaging and stochastic biology. To address this issue, we introduce the Experiment Automation Pipeline for Event-Driven Microscopy to Smart Microfluidic Single-Cells Analysis (EAP4EMSIG). In particular, we present initial zero-shot results from the real-time segmentation module of our approach. Our findings indicate that among four State-Of-The- Art (SOTA) segmentation methods evaluated, Omnipose delivers the highest Panoptic Quality (PQ) score of 0.9336, while Contour Proposal Network (CPN) achieves the fastest inference time of 185 ms with the second-highest PQ score of 0.8575. Furthermore, we observed that the vision foundation model Segment Anything is unsuitable for this particular use case.

Nils Friederich, Angelo Jovin Yamachui Sitcheu, Annika Nassal et al.

Microfluidic Live-Cell Imaging (MLCI) yields data on microbial cell factories. However, continuous acquisition is challenging as high-throughput experiments often lack real-time insights, delaying responses to stochastic events. We introduce three components in the Experiment Automation Pipeline for Event-Driven Microscopy to Smart Microfluidic Single-Cell Analysis (EAP4EMSIG): a fast, accurate Multi-Layer Perceptron (MLP)-based autofocusing method predicting the focus offset, an evaluation of real-time segmentation methods and a real-time data analysis dashboard. Our MLP-based autofocusing achieves a Mean Absolute Error (MAE) of 0.105 $μ$m with inference times from 87 ms. Among eleven evaluated Deep Learning (DL) segmentation methods, Cellpose reached a Panoptic Quality (PQ) of 93.36 %, while a distance-based method was fastest (121 ms, Panoptic Quality 93.02 %).

Christopher Hahne, Amar Aggoun, Vladan Velisavljevic et al.

In this paper, we demonstrate light field triangulation to determine depth distances and baselines in a plenoptic camera. Advances in micro lenses and image sensors have enabled plenoptic cameras to capture a scene from different viewpoints with sufficient spatial resolution. While object distances can be inferred from disparities in a stereo viewpoint pair using triangulation, this concept remains ambiguous when applied in the case of plenoptic cameras. We present a geometrical light field model allowing the triangulation to be applied to a plenoptic camera in order to predict object distances or specify baselines as desired. It is shown that distance estimates from our novel method match those of real objects placed in front of the camera. Additional benchmark tests with an optical design software further validate the model's accuracy with deviations of less than +-0.33 % for several main lens types and focus settings. A variety of applications in the automotive and robotics field can benefit from this estimation model.