Evidence map›Paper›PMID 37381218›Full record

ArticleOptics express2023

Functional imaging through scattering medium via fluorescence speckle demixing and localization.

F Soldevila, C Moretti, T Nöbauer, H Sarafraz, A Vaziri, S Gigan

Abstract read
In one paragraph

Article in Optics express, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Foveated Light-Field Compound Imager.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
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  11. Article
  12. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

F Soldevila
C Moretti
T Nöbauer
H Sarafraz
A Vaziri
S Gigan

Funding

In vivo Imaging of Neuroactivity in the Deep Forward Scattering Regime Using Speckle Identification and Demixing (SPID) MicroscopyRF1NS113251 · NINDS · ROCKEFELLER UNIVERSITY · PI GIGAN, SYLVAIN, VAZIRI, ALIPASHA · 2019 to 2019
$2.1M
NINDS NIH HHS RF1 NS113251
6 · The paper itself

Abstract

Recently, fluorescence-based optical techniques have emerged as a powerful tool to probe information in the mammalian brain. However, tissue heterogeneities prevent clear imaging of deep neuron bodies due to light scattering. While several up-to-date approaches based on ballistic light allow to retrieve information at shallow depths inside the brain, non-invasive localization and functional imaging at depth still remains a challenge. It was recently shown that functional signals from time-varying fluorescent emitters located behind scattering samples could be retrieved by using a matrix factorization algorithm. Here we show that the seemingly information-less, low-contrast fluorescent speckle patterns recovered by the algorithm can be used to locate each individual emitter, even in the presence of background fluorescence. We test our approach by imaging the temporal activity of large groups of fluorescent sources behind different scattering phantoms mimicking biological tissues, and through a brain slice with a thickness of ∼200 µm.

Indexed as

AlgorithmsDiagnostic ImagingAnimalsBrainColoring AgentsFluorescenceMammalsPhantoms, ImagingColoring Agents

Identifiers

PMID37381218
PMCPMC10316750

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.