Evidence map›Paper›PMID 35209312›Full record

ArticleOptics express2022

Scan-less machine-learning-enabled incoherent microscopy for minimally-invasive deep-brain imaging.

Ruipeng Guo, Soren Nelson, Matthew Regier, M Wayne Davis, Erik M Jorgensen, Jason Shepherd, Rajesh Menon

Open access · goldAbstract read
In one paragraph

Article in Optics express, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. 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 at 2 institutions in 1 country.

Ruipeng Guo
Soren Nelson
Matthew Regier
M Wayne Davis
Erik M Jorgensen
Jason Shepherd
Rajesh Menon
University of Utah · USHoward Hughes Medical Institute · US

Funding

Expanding field-of-view with reduced tissue displacement in micro-endoscopic computational imagingR21EY030717 · NEI · UNIVERSITY OF UTAH · PI BLAIR, STEVEN M, MENON, RAJESH · 2019 to 2019
$457k
NEI NIH HHS R21 EY030717
6 · The paper itself

Abstract

Deep-brain microscopy is strongly limited by the size of the imaging probe, both in terms of achievable resolution and potential trauma due to surgery. Here, we show that a segment of an ultra-thin multi-mode fiber (cannula) can replace the bulky microscope objective inside the brain. By creating a self-consistent deep neural network that is trained to reconstruct anthropocentric images from the raw signal transported by the cannula, we demonstrate a single-cell resolution (< 10μm), depth sectioning resolution of 40 μm, and field of view of 200 μm, all with green-fluorescent-protein labelled neurons imaged at depths as large as 1.4 mm from the brain surface. Since ground-truth images at these depths are challenging to obtain in vivo, we propose a novel ensemble method that averages the reconstructed images from disparate deep-neural-network architectures. Finally, we demonstrate dynamic imaging of moving GCaMp-labelled C. elegans worms. Our approach dramatically simplifies deep-brain microscopy.

Indexed as

Machine LearningAnimalsBrainCaenorhabditis elegansCells, CulturedGreen Fluorescent ProteinsImage Processing, Computer-AssistedMiceMicroscopy, FluorescenceMinimally Invasive Surgical ProceduresNeural Networks, ComputerNeuroimagingNeuronsGreen Fluorescent Proteins

Identifiers

PMID35209312
PMCPMC8970698
OpenAlexW4200520941

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.