Evidence map›Paper›PMID 42154674›Full record

ArticlePloS one2026

Performance evaluation of a novel fully-automated molecular diagnostics system Molecision R8.

Yanfang Mo, Xiaowen Wu, Chao Chen, Lixia Liang, Jianyin Su, Chengde Li, Yueying Wang, Ting Wang, Pu Sun, Zhonggang Fang and 1 more

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2026. 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

11 authors.

Yanfang MoDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Xiaowen WuDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Chao ChenResearch and Development Department, Shenzhen New Industries Biomedical Engineering Co., Ltd, Shenzhen, China.
Lixia LiangDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Jianyin SuDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Chengde LiDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Yueying WangDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Ting WangResearch and Development Department, Shenzhen New Industries Biomedical Engineering Co., Ltd, Shenzhen, China.
Pu SunResearch and Development Department, Shenzhen New Industries Biomedical Engineering Co., Ltd, Shenzhen, China.
Zhonggang FangResearch and Development Department, Shenzhen New Industries Biomedical Engineering Co., Ltd, Shenzhen, China.ORCID https://orcid.org/0009-0006-5502-110X
Zhifang LinDepartment of Clinical Laboratory, The First People's Hospital of Zhaoqing, Zhaoqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the functionality of key modules of a novel fully-automated molecular diagnostics system Molecision R8 and the performance of the integrated system.

methodsThe nucleic acid extraction and PCR detection modules were evaluated using HBV DNA assay through precision and comparison with Molecision MP-32 and HongShi SLAN-96, respectively. Instrument comparison of R8 with an open system was conducted using Molecision HBV DNA and Chlamydia trachomatis/Ureaplasma urealyticum/Neisseria gonorrhoeae (CT/UU/NG) triplex assays. Systemic comparison of R8 and combined reagents with Sansure system were conducted on HBV DNA, CT, UU, and NG assays of their own.

resultsIn modular evaluation, the imprecision of both modules was all below 5% and Passing-Bablok (PB) regression and Bland-Altman (BA) analysis showed closeness to y = x and biases below 0.15 lg IU/mL. Instrument comparison obtained a regression equation of y = 0.982x + 0.084 and a bias of 0.05 lg IU/mL for HBV DNA detection in serum and agreement rates all above 96.5% for CT, UU and NG detection in genital tract samples. In the systemic comparison, the regression equation was y = 1.024x + 0.096 and the bias was 0 lg IU/mL for HBV DNA. For CT, UU and NG, the agreement rates were also all larger than 96.5%.

conclusionsAnalytical performance of Molecision R8 was superior or comparable to commercial nucleic acid purification and PCR systems. Molecision R8 alone or combined with related reagents are robust in measuring serum and genital tract samples. Overall, Molecision R8 holds strong promise for clinical use.

Indexed as

Molecular Diagnostic TechniquesAutomationChlamydia trachomatisDNA, BacterialDNA, ViralFemaleHepatitis B virusHumansNeisseria gonorrhoeaePolymerase Chain ReactionDNA, BacterialDNA, Viral

Identifiers

PMID42154674
PMCPMC13186364

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.