Evidence map›Paper›PMID 38505412›Full record

ReviewBiophysics reviews2022

Live cell microscopy: From image to insight.

Andreas P Cuny, Fabian P Schlottmann, Jennifer C Ewald, Serge Pelet, Kurt M Schmoller

Abstract readReview
In one paragraph

Review in Biophysics reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Fabian P SchlottmannInterfaculty Institute of Cell Biology, University of Tuebingen, 72076 Tuebingen, Germany.ORCID https://orcid.org/0000-0001-6340-2742
Jennifer C EwaldInterfaculty Institute of Cell Biology, University of Tuebingen, 72076 Tuebingen, Germany.ORCID https://orcid.org/0000-0003-1822-4988
Serge PeletDepartment of Fundamental Microbiology, University of Lausanne, 1015 Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-0245-049X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Live-cell microscopy is a powerful tool that can reveal cellular behavior as well as the underlying molecular processes. A key advantage of microscopy is that by visualizing biological processes, it can provide direct insights. Nevertheless, live-cell imaging can be technically challenging and prone to artifacts. For a successful experiment, many careful decisions are required at all steps from hardware selection to downstream image analysis. Facing these questions can be particularly intimidating due to the requirement for expertise in multiple disciplines, ranging from optics, biophysics, and programming to cell biology. In this review, we aim to summarize the key points that need to be considered when setting up and analyzing a live-cell imaging experiment. While we put a particular focus on yeast, many of the concepts discussed are applicable also to other organisms. In addition, we discuss reporting and data sharing strategies that we think are critical to improve reproducibility in the field.

Identifiers

PMID38505412
PMCPMC10903399

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.