Evidence map›Paper›PMID 36834888›Full record

ArticleInternational journal of molecular sciences2023

Accurate Detection of SARS-CoV-2 by Next-Generation Sequencing in Low Viral Load Specimens.

Marius Ilié, Jonathan Benzaquen, Véronique Hofman, Elodie Long-Mira, Sandra Lassalle, Jacques Boutros, Christophe Bontoux, Virginie Lespinet-Fabre, Olivier Bordone, Virginie Tanga and 11 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

21 authors at 3 institutions in 1 country.

Marius IliéLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0002-2014-1236
Jonathan BenzaquenTeam 4, Institute of Research on Cancer and Aging (IRCAN), CNRS INSERM, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0002-1899-9612
Véronique HofmanLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0003-0943-1627
Elodie Long-MiraLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0002-1923-6713
Sandra LassalleLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Jacques BoutrosDepartment of Pulmonary Medicine and Oncology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0002-6468-1648
Christophe BontouxLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0001-5446-6197
Virginie Lespinet-FabreLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Olivier BordoneHospital-Related Biobank (BB-0033-00025), Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Virginie TangaHospital-Related Biobank (BB-0033-00025), Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Maryline AllegraHospital-Related Biobank (BB-0033-00025), Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Myriam SalahHospital-Related Biobank (BB-0033-00025), Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Julien FayadaHospital-Related Biobank (BB-0033-00025), Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Sylvie LeroyDepartment of Pulmonary Medicine and Oncology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.
Matteo VassalloDepartment of Internal Medicine and Oncology, Centre Hospitalier de Cannes, 06400 Cannes, France.
Irit TouitouDepartment of Infectious Diseases, Hôpital Archet 1, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, 06200 Nice, France.
Johan CourjonDepartment of Infectious Diseases, Hôpital Archet 1, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, 06200 Nice, France.
Julie ContentiEmergency Department, Hôpital Pasteur 2, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0002-1532-6180
Michel CarlesDepartment of Infectious Diseases, Hôpital Archet 1, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, 06200 Nice, France.
Charles-Hugo MarquetteTeam 4, Institute of Research on Cancer and Aging (IRCAN), CNRS INSERM, Université Côte d'Azur, 06107 Nice, France.ORCID 0000-0002-0846-9941
Paul HofmanLaboratory of Clinical and Experimental Pathology, Centre Hospitalier Universitaire de Nice, FHU OncoAge, Université Côte d'Azur, 06000 Nice, France.ORCID 0000-0003-0431-9353
Université Côte d'Azur · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier de Cannes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As new SARS-CoV-2 variants emerge, there is an urgent need to increase the efficiency and availability of viral genome sequencing, notably to detect the lineage in samples with a low viral load. SARS-CoV-2 genome next-generation sequencing (NGS) was performed retrospectively in a single center on 175 positive samples from individuals. An automated workflow used the Ion AmpliSeq SARS-CoV-2 Insight Research Assay on the Genexus Sequencer. All samples were collected in the metropolitan area of the city of Nice (France) over a period of 32 weeks (from 19 July 2021 to 11 February 2022). In total, 76% of cases were identified with a low viral load (Ct ≥ 32, and ≤200 copies/µL). The NGS analysis was successful in 91% of cases, among which 57% of cases harbored the Delta variant, and 34% the Omicron BA.1.1 variant. Only 9% of cases had unreadable sequences. There was no significant difference in the viral load in patients infected with the Omicron variant compared to the Delta variant (Ct values,

Indexed as

COVID-19SARS-CoV-2High-Throughput Nucleotide SequencingHumansRetrospective StudiesViral LoadCOVID-19Genexuslow viral loadnext generation sequencingSARS-CoV-2

Identifiers

PMID36834888
PMCPMC9964843
OpenAlexW4319983282

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.