Evidence map›Paper›PMID 31674164›Full record

ArticleJournal of biomedical optics2019

Dual-beam confocal light-sheet microscopy via flexible acousto-optic deflector.

Vladislav Gavryusev, Giuseppe Sancataldo, Pietro Ricci, Alberto Montalbano, Chiara Fornetto, Lapo Turrini, Annunziatina Laurino, Luca Pesce, Giuseppe de Vito, Natascia Tiso and 3 more

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Exploring the human cerebral cortex using confocal microscopy.Progress in biophysics and molecular biology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. 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

13 authors.

Vladislav GavryusevEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Giuseppe SancataldoEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Pietro RicciEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Alberto MontalbanoUniversity of Florence, Department of Neuroscience, Psychology, Drug Research and Child Health, Flor, Italy.
Chiara FornettoEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Lapo TurriniEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Annunziatina LaurinoEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Luca PesceEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Giuseppe de VitoEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Natascia TisoUniversity of Padova, Department of Biology, Padova, Italy.
Francesco VanziEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Ludovico SilvestriEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Francesco S PavoneEuropean Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.

Funding

Imaging and Analysis Techniques to Construct a Cell Census Atlas of the Human Brain Admin SupplementU01MH117023 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI BOAS, DAVID A, FISCHL, BRUCE · 2018 to 2022
$7.6M
European Research CouncilNIMH NIH HHS U01 MH117023
6 · The paper itself

Abstract

Confocal detection in digital scanned laser light-sheet fluorescence microscopy (DSLM) has been established as a gold standard method to improve image quality. The selective line detection of a complementary metal–oxide–semiconductor camera (CMOS) working in rolling shutter mode allows the rejection of out-of-focus and scattered light, thus reducing background signal during image formation. Most modern CMOS have two rolling shutters, but usually only a single illuminating beam is used, halving the maximum obtainable frame rate. We report on the capability to recover the full image acquisition rate via dual confocal DSLM by using an acousto-optic deflector. Such a simple solution enables us to independently generate, control and synchronize two beams with the two rolling slits on the camera. We show that the doubling of the imaging speed does not affect the confocal detection high contrast.

Indexed as

AnimalsBrainEquipment DesignHigh-Throughput Screening AssaysImage Processing, Computer-AssistedLarvaMiceMice, Inbred C57BLMicroscopy, ConfocalMicroscopy, FluorescenceZebrafishacousto-optic deflectorconfocal detectiondigital scanned laser light-sheet fluorescence microscopyhigh contrasthigh-throughput microscopylight-sheet microscopymouse brainzebrafish brain

Identifiers

PMID31674164
PMCPMC7000876

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.