Evidence map›Paper›PMID 38456096›Full record

ArticleInternational journal of analytical chemistry2024

Development of a Novel Multiplex PCR Method for the Rapid Detection of SARS-CoV-2, Influenza A Virus, and Influenza B Virus.

Liang Ma, Haoyan Zhu, Yongwei Jiang, Xiaomu Kong, Peng Gao, Yi Liu, Meimei Zhao, Guoxiong Deng, Yongtong Cao

Open access · goldAbstract read
In one paragraph

Article in International journal of analytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 1 institution in 1 country.

Liang MaDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0003-3226-4150
Haoyan ZhuDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.
Yongwei JiangDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-4974-0283
Xiaomu KongDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-5920-4759
Peng GaoDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-7096-2710
Yi LiuDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-5743-0621
Meimei ZhaoDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-6031-5544
Guoxiong DengDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.
Yongtong CaoDepartment of Clinical Laboratory, China-Japan Friendship Hospital, Beijing 100029, China.ORCID https://orcid.org/0000-0002-8904-3060
China-Japan Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: A sensitive and specific multiplex fluorescence rapid detection method was established for simultaneous detection of SARS-CoV-2, influenza A virus, and influenza B virus in a self-made device within 30 min, with a minimum detection limit of 200 copies/mL. Methods: Based on the genome sequences of SARS-CoV-2, influenza A virus (FluA), and influenza B virus (FluB) with reference to the Chinese Center for Disease Control and Prevention and related literature, specific primers were designed, and a multiplex fluorescent PCR system was established. The simultaneous and rapid detection of SARS-CoV-2, FluA, and FluB was achieved by optimizing the concentrations of Taq DNA polymerase as well as primers, probes, and Mg Results: By optimizing the amplification system, the N enzyme with the best amplification performance was selected, and the optimal concentration of Mg Conclusion: A multiplex real-time quantitative fluorescence RT-PCR system for three respiratory viruses of SARS-CoV-2, FluA, and FluB was established with a high amplification efficiency and sensitivity reaching 200 copies/mL for all samples. Combined with the automated microfluidic nucleic acid detection system, the system can achieve rapid detection in 30 minutes.

Identifiers

PMID38456096
PMCPMC10919977
OpenAlexW4392282414

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.