Evidence map›Paper›PMID 37066401›Full record

ArticlebioRxiv : the preprint server for biology2024

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

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

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Ryan ThiermannDepartment of Physics, University of California San Diego, La Jolla CA.ORCID 0000-0002-0348-4181
Michael SandlerDepartment of Physics, University of California San Diego, La Jolla CA.
Gursharan AhirDepartment of Physics, University of California San Diego, La Jolla CA.
John T SaulsDepartment of Physics, University of California San Diego, La Jolla CA.
Jeremy W SchroederDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI.
Steven D BrownDepartment of Physics, University of California San Diego, La Jolla CA.
Guillaume Le TreutChan Zuckerberg Biohub, San Francisco, CA.
Fangwei SiDepartment of Physics, Carnegie Mellon University, Pittsburgh, PA.
Dongyang LiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA.
Jue D WangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI.ORCID 0000-0003-1503-170X
Suckjoon JunDepartment of Physics, University of California San Diego, La Jolla CA.ORCID 0000-0002-0139-4297

Funding

The critical roles of (p)ppGpp in homeostasis and antibiotic tolerance in Gram positive bacteriaR35GM127088 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Jue D. Wang · 2018 to 2026
$3.9M
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 GM127088NIGMS NIH HHS R35 GM139622
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) - i.e., 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.

Identifiers

PMID37066401
PMCPMC10103947

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.