Evidence map›Paper›PMID 32572233›Full record

ArticleNature methods2020

Homogeneous multifocal excitation for high-throughput super-resolution imaging.

Dora Mahecic, Davide Gambarotto, Kyle M Douglass, Denis Fortun, Niccoló Banterle, Khalid A Ibrahim, Maeva Le Guennec, Pierre Gönczy, Virginie Hamel, Paul Guichard and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
10.4field-weighted citation impact, top 2% of its field
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

31 citing papers in PubMed, 93 citations in OpenAlex.

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  14. bioRxiv : the preprint server for biology · 2023
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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

11 authors at 4 institutions in 2 countries.

Dora MahecicLaboratory for Experimental Biophysics, Institute of Physics, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland. dora.mahecic@epfl.ch.ORCID http://orcid.org/0000-0003-1004-4771
Davide GambarottoDepartment of Cell Biology, Sciences III, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0003-4691-082X
Kyle M DouglassLaboratory for Experimental Biophysics, Institute of Physics, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland.
Denis FortunICube UMR 7357, CNRS, University of Strasbourg, Illkirch, France.
Niccoló BanterleSwiss Institute for Experimental Cancer Research, School of Life Sciences, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland.ORCID http://orcid.org/0000-0002-1607-0324
Khalid A IbrahimLaboratory for Experimental Biophysics, Institute of Physics, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland.ORCID http://orcid.org/0000-0003-1819-1952
Maeva Le GuennecDepartment of Cell Biology, Sciences III, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0002-3789-7988
Pierre GönczySwiss National Centre for Competence in Research (NCCR) in Chemical Biology, University of Geneva, Geneva, Switzerland.
Virginie HamelDepartment of Cell Biology, Sciences III, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0001-5092-2343
Paul GuichardDepartment of Cell Biology, Sciences III, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0002-0363-1049
Suliana ManleyLaboratory for Experimental Biophysics, Institute of Physics, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland. suliana.manley@epfl.ch.ORCID http://orcid.org/0000-0002-4755-4778
University of Geneva · CHNCCR Chemical Biology - Visualisation and Control of Biological Processes Using Chemistry · CHÉcole Polytechnique Fédérale de Lausanne · CHCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Super-resolution microscopies have become an established tool in biological research. However, imaging throughput remains a main bottleneck in acquiring large datasets required for quantitative biology. Here we describe multifocal flat illumination for field-independent imaging (mfFIFI). By integrating mfFIFI into an instant structured illumination microscope (iSIM), we extend the field of view (FOV) to >100 × 100 µm

Indexed as

AnimalsCentriolesChlorocebus aethiopsCOS CellsHumansImaging, Three-DimensionalLightingMicroscopy, FluorescenceMicrotubules

Identifiers

PMID32572233
OpenAlexW3035805368

What OpenQuestion holds

Textmetadata
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.