Evidence map›Paper›PMID 38634855›Full record

ArticleeLife2024

Tools and methods for high-throughput single-cell imaging with the mother machine.

Ryan Thiermann, Michael Sandler, Gursharan Ahir, John T Sauls, Jeremy Schroeder, Steven Brown, Guillaume Le Treut, Fangwei Si, Dongyang Li, Jue D Wang and 1 more

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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  5. Article
  6. Article
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  9. Dispensability of extrinsic DnaA regulators inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Microbial life in slow and stopped lanes.Trends in microbiology · 2024
    Review
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Ryan Thiermann *Department of Physics, University of California, San Diego, La Jolla, United States.ORCID https://orcid.org/0000-0002-0348-4181
Michael Sandler *Department of Physics, University of California, San Diego, La Jolla, United States.
Gursharan Ahir *Department of Physics, University of California, San Diego, La Jolla, United States.
John T Sauls *Department of Physics, University of California, San Diego, La Jolla, United States.
Jeremy Schroeder *Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, United States.ORCID https://orcid.org/0000-0001-8829-8494
Steven BrownDepartment of Physics, University of California, San Diego, La Jolla, United States.
Guillaume Le TreutChan Zuckerberg Biohub, San Francisco, United States.
Fangwei SiDepartment of Physics, Carnegie Mellon University, Pittsburgh, United States.
Dongyang LiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Jue D WangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, United States.ORCID https://orcid.org/0000-0003-1503-170X
Suckjoon JunDepartment of Physics, University of California, San Diego, La Jolla, United States.ORCID https://orcid.org/0000-0002-0139-4297

Funding

Control of cellular resource allocation across biological scales in microorganismsR35GM139622 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JUN, SUCKJOON · 2021 to 2025
$2.3M
NIGMS NIH HHS R35 GM139622NIGMS NIH HHS R35GM139622
6 · The paper itself

Abstract

Despite much progress, image processing remains a significant bottleneck for high-throughput analysis of microscopy data. One popular platform for single-cell time-lapse imaging is the mother machine, which enables long-term tracking of microbial cells under precisely controlled growth conditions. While several mother machine image analysis pipelines have been developed in the past several years, adoption by a non-expert audience remains a challenge. To fill this gap, we implemented our own software, MM3, as a plugin for the multidimensional image viewer napari. napari-MM3 is a complete and modular image analysis pipeline for mother machine data, which takes advantage of the high-level interactivity of napari. Here, we give an overview of napari-MM3 and test it against several well-designed and widely used image analysis pipelines, including BACMMAN and DeLTA. Researchers often analyze mother machine data with custom scripts using varied image analysis methods, but a quantitative comparison of the output of different pipelines has been lacking. To this end, we show that key single-cell physiological parameter correlations and distributions are robust to the choice of analysis method. However, we also find that small changes in thresholding parameters can systematically alter parameters extracted from single-cell imaging experiments. Moreover, we explicitly show that in deep learning-based segmentation, 'what you put is what you get' (WYPIWYG) - that is, pixel-level variation in training data for cell segmentation can propagate to the model output and bias spatial and temporal measurements. Finally, while the primary purpose of this work is to introduce the image analysis software that we have developed over the last decade in our lab, we also provide information for those who want to implement mother machine-based high-throughput imaging and analysis methods in their research.

Indexed as

Image Processing, Computer-AssistedMothersCultureFemaleHumansMicroscopyResearch Personnelbacterial physiologyE. coliimage analysisinfectious diseasemicrobiologymicrofluidicsmother machine

Identifiers

PMID38634855
PMCPMC11026091

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.