Evidence map›Paper›PMID 37475960›Full record

ArticleFrontiers in cellular and infection microbiology2023

Evaluation of an identification method for the SARS-CoV-2 Delta variant based on the amplification-refractory mutation system.

Qin Zhang, Runjie Qiao, Jiaojiao Niu, Xia Xiong, Nan Wang, Ruixian Zhang, Sha Luo, Yuwan Guo, Zhonghua Liu, Li Peng and 7 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Qin ZhangThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Runjie QiaoThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Jiaojiao NiuThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Xia XiongThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Nan WangThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Ruixian ZhangThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Sha LuoThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Yuwan GuoResearch and Development Department, Jiangsu Bioperfectus Technologies Company Limited, Taizhou, Jiangsu, China.
Zhonghua LiuResearch and Development Department, Jiangsu Bioperfectus Technologies Company Limited, Taizhou, Jiangsu, China.
Li PengResearch and Development Department, Jiangsu Bioperfectus Technologies Company Limited, Taizhou, Jiangsu, China.
Shaoduo ZhangResearch and Development Department, Jiangsu Bioperfectus Technologies Company Limited, Taizhou, Jiangsu, China.
Guolei TanThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Keyu SongThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Mei SunThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Lulu XuThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Rong ZhangResearch and Development Department, Jiangsu Bioperfectus Technologies Company Limited, Taizhou, Jiangsu, China.
Xuping WuThe Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Delta variant of SARS-CoV-2 dominated the COVID-19 pandemic due to its high viral replication capacity and immune evasion, causing massive outbreaks of cases, hospitalizations, and deaths. Currently, variant identification is performed mainly by sequencing. However, the high requirements for equipment and operators as well as its high cost have limited its application in underdeveloped regions. To achieve an economical and rapid method of variant identification suitable for undeveloped areas, we applied an amplification-refractory mutation system (ARMS) based on PCR for the detection of novel coronavirus variants. The results showed that this method could be finished in 90 min and detect as few as 500 copies/mL and not react with SARS-Coronavirus, influenza

Indexed as

COVID-19Influenza A Virus, H1N1 SubtypeHumansInterferon-alphaMutationPandemicsSARS-CoV-2Interferon-alphaamplification-refractory mutation systemDelta variantmolecular identificationSARS-CoV-2variant identification

Identifiers

PMID37475960
PMCPMC10354518

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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.