Evidence map›Paper›PMID 36047372›Full record

ArticleLab on a chip2022

Point-of-care SARS-CoV-2 sensing using lens-free imaging and a deep learning-assisted quantitative agglutination assay.

Colin J Potter, Yanmei Hu, Zhen Xiong, Jun Wang, Euan McLeod

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

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  5. Biomedical optics express · 2024
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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

5 authors at 1 institution in 1 country.

Colin J PotterWyant College of Optical Sciences, University of Arizona, Tucson, Arizona 85721, USA. euanmc@optics.arizona.edu.ORCID 0000-0003-3124-852X
Yanmei HuDepartment of Pharmacology, University of Arizona, Tucson, Arizona 85724, USA.
Zhen XiongWyant College of Optical Sciences, University of Arizona, Tucson, Arizona 85721, USA. euanmc@optics.arizona.edu.ORCID 0000-0001-6685-9676
Jun WangDepartment of Pharmacology, University of Arizona, Tucson, Arizona 85724, USA.ORCID 0000-0002-4845-4621
Euan McLeodWyant College of Optical Sciences, University of Arizona, Tucson, Arizona 85721, USA. euanmc@optics.arizona.edu.ORCID 0000-0002-6327-3642
University of Arizona · US

Funding

Translational research in Alzheimer’s Disease and Related Dementias (TRADD)T32AG061897 · NIA · UNIVERSITY OF ARIZONA · PI BRINTON, ROBERTA EILEEN · 2018 to 2022
$1.3M
NIA NIH HHS T32 AG061897
6 · The paper itself

Abstract

The persistence of the global COVID-19 pandemic caused by the SARS-CoV-2 virus has continued to emphasize the need for point-of-care (POC) diagnostic tests for viral diagnosis. The most widely used tests, lateral flow assays used in rapid antigen tests, and reverse-transcriptase real-time polymerase chain reaction (RT-PCR), have been instrumental in mitigating the impact of new waves of the pandemic, but fail to provide both sensitive and rapid readout to patients. Here, we present a portable lens-free imaging system coupled with a particle agglutination assay as a novel biosensor for SARS-CoV-2. This sensor images and quantifies individual microbeads undergoing agglutination through a combination of computational imaging and deep learning as a way to detect levels of SARS-CoV-2 in a complex sample. SARS-CoV-2 pseudovirus in solution is incubated with acetyl cholinesterase 2 (ACE2)-functionalized microbeads then loaded into an inexpensive imaging chip. The sample is imaged in a portable in-line lens-free holographic microscope and an image is reconstructed from a pixel superresolved hologram. Images are analyzed by a deep-learning algorithm that distinguishes microbead agglutination from cell debris and viral particle aggregates, and agglutination is quantified based on the network output. We propose an assay procedure using two images which results in the accurate determination of viral concentrations greater than the limit of detection (LOD) of 1.27 × 10

Indexed as

COVID-19Deep LearningAgglutinationAngiotensin-Converting Enzyme 2COVID-19 TestingDNA-Directed RNA PolymerasesHumansPandemicsPoint-of-Care SystemsSARS-CoV-2Sensitivity and SpecificityAngiotensin-Converting Enzyme 2DNA-Directed RNA Polymerases

Identifiers

PMID36047372
PMCPMC9529856
OpenAlexW4293200632

What OpenQuestion holds

Textmetadata
LicenceTDM
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.