Evidence map›Paper›PMID 25475544›Full record

ArticleScientific reports2014

fM to aM nucleic acid amplification for molecular diagnostics in a non-stick-coated metal microfluidic bioreactor.

Guoliang Huang, Qin Huang, Li Ma, Xianbo Luo, Biao Pang, Zhixin Zhang, Ruliang Wang, Junqi Zhang, Qi Li, Rongxin Fu and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2014. 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.

Guoliang Huang1] Department of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China [2] National Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Qin HuangNational Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Li MaNational Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Xianbo LuoNational Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Biao PangNational Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Zhixin ZhangNational Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China.
Ruliang WangDepartment of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China.
Junqi ZhangDepartment of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China.
Qi LiDepartment of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China.
Rongxin FuDepartment of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China.
Jiancheng YeDepartment of Biomedical Engineering, the School of Medicine, Tsinghua University, Beijing 100084, China.

Funding

Analysis: Emotion-Based Alcohol Consumption with fMRI and Experimental ParadigmK01AA020102 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI CYDERS, MELISSA A · 2011 to 2015
$770k
NIAAA NIH HHS K01 AA020102
6 · The paper itself

Abstract

A sensitive DNA isothermal amplification method for the detection of DNA at fM to aM concentrations for pathogen identification was developed using a non-stick-coated metal microfluidic bioreactor. A portable confocal optical detector was utilized to monitor the DNA amplification in micro- to nanoliter reaction assays in real-time, with fluorescence collection near the optical diffraction limit. The non-stick-coated metal microfluidic bioreactor, with a surface contact angle of 103°, was largely inert to bio-molecules, and DNA amplification could be performed in a minimum reaction volume of 40 nL. The isothermal nucleic acid amplification for Mycoplasma pneumoniae identification in the non-stick-coated microfluidic bioreactor could be performed at a minimum DNA template concentration of 1.3 aM, and a detection limit of three copies of genomic DNA was obtained. This microfluidic bioreactor offers a promising clinically relevant pathogen molecular diagnostic method via the amplification of targets from only a few copies of genomic DNA from a single bacterium.

Indexed as

BioreactorsDNA, BacterialEquipment DesignEquipment Failure AnalysisMicrofluidic Analytical TechniquesMolecular Diagnostic TechniquesMycoplasma pneumoniaeNucleic Acid Amplification TechniquesReproducibility of ResultsSensitivity and SpecificitySequence Analysis, DNADNA, Bacterial

Identifiers

PMID25475544
PMCPMC5384283

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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.