Evidence map›Paper›PMID 30224740›Full record

ArticleScientific reports2018

Multidirectional digital scanned light-sheet microscopy enables uniform fluorescence excitation and contrast-enhanced imaging.

Adam K Glaser, Ye Chen, Chengbo Yin, Linpeng Wei, Lindsey A Barner, Nicholas P Reder, Jonathan T C Liu

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

7 authors.

Adam K GlaserDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA. akglaser@uw.edu.
Ye ChenDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA.
Chengbo YinDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA.
Linpeng WeiDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA.ORCID 0000-0003-3257-7691
Lindsey A BarnerDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA.
Nicholas P RederDepartment of Pathology, University of Washington, Seattle, WA, USA.
Jonathan T C LiuDepartment of Mechanical Engineering, University of Washington, Seattle, WA, USA. jonliu@uw.edu.ORCID 0000-0001-5650-3086

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Line-scanned MEMS-based dual-axis confocal microscopy to detect oral lesions in vR01DE023497 · NIDCR · UNIVERSITY OF WASHINGTON · PI LIU, JONATHAN T.C. · 2012 to 2014
$2.4M
Intraoperative confocal microscopy for quantitative delineation of low-grade glioR01CA175391 · NCI · UNIVERSITY OF WASHINGTON · PI LIU, JONATHAN T.C., SANAI, NADER · 2014 to 2018
$1.7M
Light-sheet microscopy (LSM) for rapid wide-area imaging and pathology of bread-loafed prostate specimensF32CA213615 · NCI · UNIVERSITY OF WASHINGTON · PI GLASER, ADAM K · 2017 to 2019
$134k
NCI NIH HHS F32 CA213615NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA175391NIDCR NIH HHS R01 DE023497
6 · The paper itself

Abstract

Light-sheet fluorescence microscopy (LSFM) has emerged as a powerful method for rapid and optically efficient 3D microscopy. Initial LSFM designs utilized a static sheet of light, termed selective plane illumination microscopy (SPIM), which exhibited shadowing artifacts and deteriorated contrast due to light scattering. These issues have been addressed, in part, by multidirectional selective plane illumination microscopy (mSPIM), in which rotation of the light sheet is used to mitigate shadowing artifacts, and digital scanned light-sheet microscopy (DSLM), in which confocal line detection is used to reject scattered light. Here we present a simple and passive multidirectional digital scanned light-sheet microscopy (mDSLM) architecture that combines the benefits of mSPIM and DSLM. By utilizing an elliptical Gaussian beam with increased angular diversity in the imaging plane, mDSLM provides mitigation of shadowing artifacts and contrast-enhanced imaging of fluorescently labeled samples.

Indexed as

AnimalsArtifactsFluorescenceHumansImage Processing, Computer-AssistedMiceMicroscopy, Fluorescence

Identifiers

PMID30224740
PMCPMC6141597

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.