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Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC
BACKGROUND: High-throughput live-cell imaging is a powerful tool to study dynamic cellular processes in single cells but creates a bottleneck at the stage of data analysis, due to the large amount of data generated and limitations of analytical pipelines. Recent progress on deep learning dramaticall...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356409/ https://www.ncbi.nlm.nih.gov/pubmed/35932043 http://dx.doi.org/10.1186/s12915-022-01372-6 |
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author | Padovani, Francesco Mairhörmann, Benedikt Falter-Braun, Pascal Lengefeld, Jette Schmoller, Kurt M. |
author_facet | Padovani, Francesco Mairhörmann, Benedikt Falter-Braun, Pascal Lengefeld, Jette Schmoller, Kurt M. |
author_sort | Padovani, Francesco |
collection | PubMed |
description | BACKGROUND: High-throughput live-cell imaging is a powerful tool to study dynamic cellular processes in single cells but creates a bottleneck at the stage of data analysis, due to the large amount of data generated and limitations of analytical pipelines. Recent progress on deep learning dramatically improved cell segmentation and tracking. Nevertheless, manual data validation and correction is typically still required and tools spanning the complete range of image analysis are still needed. RESULTS: We present Cell-ACDC, an open-source user-friendly GUI-based framework written in Python, for segmentation, tracking and cell cycle annotations. We included state-of-the-art deep learning models for single-cell segmentation of mammalian and yeast cells alongside cell tracking methods and an intuitive, semi-automated workflow for cell cycle annotation of single cells. Using Cell-ACDC, we found that mTOR activity in hematopoietic stem cells is largely independent of cell volume. By contrast, smaller cells exhibit higher p38 activity, consistent with a role of p38 in regulation of cell size. Additionally, we show that, in S. cerevisiae, histone Htb1 concentrations decrease with replicative age. CONCLUSIONS: Cell-ACDC provides a framework for the application of state-of-the-art deep learning models to the analysis of live cell imaging data without programming knowledge. Furthermore, it allows for visualization and correction of segmentation and tracking errors as well as annotation of cell cycle stages. We embedded several smart algorithms that make the correction and annotation process fast and intuitive. Finally, the open-source and modularized nature of Cell-ACDC will enable simple and fast integration of new deep learning-based and traditional methods for cell segmentation, tracking, and downstream image analysis. Source code: https://github.com/SchmollerLab/Cell_ACDC SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01372-6. |
format | Online Article Text |
id | pubmed-9356409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93564092022-08-07 Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC Padovani, Francesco Mairhörmann, Benedikt Falter-Braun, Pascal Lengefeld, Jette Schmoller, Kurt M. BMC Biol Software BACKGROUND: High-throughput live-cell imaging is a powerful tool to study dynamic cellular processes in single cells but creates a bottleneck at the stage of data analysis, due to the large amount of data generated and limitations of analytical pipelines. Recent progress on deep learning dramatically improved cell segmentation and tracking. Nevertheless, manual data validation and correction is typically still required and tools spanning the complete range of image analysis are still needed. RESULTS: We present Cell-ACDC, an open-source user-friendly GUI-based framework written in Python, for segmentation, tracking and cell cycle annotations. We included state-of-the-art deep learning models for single-cell segmentation of mammalian and yeast cells alongside cell tracking methods and an intuitive, semi-automated workflow for cell cycle annotation of single cells. Using Cell-ACDC, we found that mTOR activity in hematopoietic stem cells is largely independent of cell volume. By contrast, smaller cells exhibit higher p38 activity, consistent with a role of p38 in regulation of cell size. Additionally, we show that, in S. cerevisiae, histone Htb1 concentrations decrease with replicative age. CONCLUSIONS: Cell-ACDC provides a framework for the application of state-of-the-art deep learning models to the analysis of live cell imaging data without programming knowledge. Furthermore, it allows for visualization and correction of segmentation and tracking errors as well as annotation of cell cycle stages. We embedded several smart algorithms that make the correction and annotation process fast and intuitive. Finally, the open-source and modularized nature of Cell-ACDC will enable simple and fast integration of new deep learning-based and traditional methods for cell segmentation, tracking, and downstream image analysis. Source code: https://github.com/SchmollerLab/Cell_ACDC SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01372-6. BioMed Central 2022-08-05 /pmc/articles/PMC9356409/ /pubmed/35932043 http://dx.doi.org/10.1186/s12915-022-01372-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Software Padovani, Francesco Mairhörmann, Benedikt Falter-Braun, Pascal Lengefeld, Jette Schmoller, Kurt M. Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title | Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title_full | Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title_fullStr | Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title_full_unstemmed | Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title_short | Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC |
title_sort | segmentation, tracking and cell cycle analysis of live-cell imaging data with cell-acdc |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356409/ https://www.ncbi.nlm.nih.gov/pubmed/35932043 http://dx.doi.org/10.1186/s12915-022-01372-6 |
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