Evidence map›Paper›PMID 39384765›Full record

ArticleLight, science & applications2024

Extended-depth of field random illumination microscopy, EDF-RIM, provides super-resolved projective imaging.

Lorry Mazzella, Thomas Mangeat, Guillaume Giroussens, Benoit Rogez, Hao Li, Justine Creff, Mehdi Saadaoui, Carla Martins, Ronan Bouzignac, Simon Labouesse and 5 more

Abstract read
In one paragraph

Article in Light, science & applications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

15 authors.

Lorry Mazzella *Aix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.
Thomas Mangeat *LITC Core Facility, Centre de Biologie Integrative (CBI), CNRS, Université de Toulouse, UT3, Toulouse, France.
Guillaume GiroussensAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.
Benoit RogezAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.
Hao LiMCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse, UT3, Toulouse, France.
Justine CreffMCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse, UT3, Toulouse, France.
Mehdi SaadaouiAix Marseille University, CNRS, IBDM UMR7288, Turing Centre for Living Systems, Marseille, France.
Carla MartinsAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.
Ronan BouzignacMCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse, UT3, Toulouse, France.
Simon LabouesseLITC Core Facility, Centre de Biologie Integrative (CBI), CNRS, Université de Toulouse, UT3, Toulouse, France.
Jérome IdierLS2N, CNRS UMR 6004, F44321, Nantes Cedex 3, France.
Frédéric GallandAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.
Marc AllainAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France.ORCID http://orcid.org/0000-0002-4922-7092
Anne SentenacAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France. anne.sentenac@fresnel.fr.
Loïc LeGoffAix Marseille Université, CNRS, Centrale Med, Institut Fresnel UMR7249, Turing Center for Living Systems, Marseille, France. loic.le-goff@univ-amu.fr.ORCID http://orcid.org/0000-0003-4114-971X

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-16-CONV-0001Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE45-0024Agence Nationale de la Recherche (French National Research Agency) ANR-21-ESRE-0002Agence Nationale de la Recherche (French National Research Agency) ANR-22-CE13-0039Agence Nationale de la Recherche (French National Research Agency) ANR-22-CE42-0010Agence Nationale de la Recherche (French National Research Agency) ANR-22-CE42-0026
6 · The paper itself

Abstract

The ultimate aim of fluorescence microscopy is to achieve high-resolution imaging of increasingly larger biological samples. Extended depth of field presents a potential solution to accelerate imaging of large samples when compression of information along the optical axis is not detrimental to the interpretation of images. We have implemented an extended depth of field (EDF) approach in a random illumination microscope (RIM). RIM uses multiple speckled illuminations and variance data processing to double the resolution. It is particularly adapted to the imaging of thick samples as it does not require the knowledge of illumination patterns. We demonstrate highly-resolved projective images of biological tissues and cells. Compared to a sequential scan of the imaged volume with conventional 2D-RIM, EDF-RIM allows an order of magnitude improvement in speed and light dose reduction, with comparable resolution. As the axial information is lost in an EDF modality, we propose a method to retrieve the sample topography for samples that are organized in cell sheets.

Identifiers

PMID39384765
PMCPMC11479626

What OpenQuestion holds

Textmetadata
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.