Evidence map›Paper›PMID 35493369›Full record

ArticleFrontiers in public health2022

Halo-A Universal Fluorescence Reader Based Threat Agent Detection Platform-A Proof of Concept Study Using SARS-CoV-2 Assays.

Joseph Walish, Jason Cox, Jeremy Boone, Jennifer Stone, Nathan Henderson, Molly Maloney, Joe Ma, Jonathan Maa, Nghiem On, Konrad Petre and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Joseph WalishC2Sense, Inc., Watertown, MA, United States.
Jason CoxC2Sense, Inc., Watertown, MA, United States.
Jeremy BooneMRIGlobal, Kansas City, MO, United States.
Jennifer StoneMRIGlobal, Kansas City, MO, United States.
Nathan HendersonMRIGlobal, Kansas City, MO, United States.
Molly MaloneyMRIGlobal, Kansas City, MO, United States.
Joe MaMaxim Biomedical, Inc., Rockville, MD, United States.
Jonathan MaaMaxim Biomedical, Inc., Rockville, MD, United States.
Nghiem OnMaxim Biomedical, Inc., Rockville, MD, United States.
Konrad PetreMaxim Biomedical, Inc., Rockville, MD, United States.
Bruce G GoodwinJoint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO-CBRND), Joint Project Lead for CBRND Enabling Biotechnologies (JPL CBRND EB), Frederick, MD, United States.
Shanmuga SozhamannanJoint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO-CBRND), Joint Project Lead for CBRND Enabling Biotechnologies (JPL CBRND EB), Frederick, MD, United States.
Robert DeansC2Sense, Inc., Watertown, MA, United States.
Maxim Integrated (United States) · USMRIGlobal · USLogistics Management Institute (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymerase chain reaction (PCR) remains the gold standard in disease diagnostics due to its extreme sensitivity and specificity. However, PCR tests are expensive and complex, require skilled personnel and specialized equipment to conduct the tests, and have long turnaround times. On the other hand, lateral flow immunoassay-based antigen tests are rapid, relatively inexpensive, and can be performed by untrained personnel at the point of care or even in the home. However, rapid antigen tests are less sensitive than PCR since they lack the inherent target amplification of PCR. It has been argued that rapid antigen tests are better indicators of infection in public health decision-making processes to test, trace, and isolate infected people to curtail further transmission. Hence, there is a critical need to increase the sensitivity of rapid antigen tests and create innovative solutions to achieve that goal. Herein, we report the development of a low-cost diagnostic platform, enabling rapid detection of SARS-CoV-2 under field or at-home conditions. This platform (Halo™) is a small, highly accurate, consumer-friendly diagnostic reader paired with fluorescently labeled lateral flow assays and custom software for collection and reporting of results. The focus of this study is to compare the analytical performance of Halo

Indexed as

COVID-19Metal NanoparticlesGoldHumansProof of Concept StudySARS-CoV-2Golddiagnosticseuropiumfluorescencehandheld readerimmunoassaymobile apprapid antigen testSARS-CoV-2

Identifiers

PMID35493369
PMCPMC9039038
OpenAlexW4223499801

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.