Evidence map›Paper›PMID 32834504›Full record

ArticleSensors and actuators. B, Chemical2020

All-fiber all-optical quantitative polymerase chain reaction (qPCR).

Xuegang Li, Linh V Nguyen, Kelly Hill, Heike Ebendorff-Heidepriem, Erik P Schartner, Yong Zhao, Xue Zhou, Yanan Zhang, Stephen C Warren-Smith

Abstract read
In one paragraph

Article in Sensors and actuators. B, Chemical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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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.

Xuegang LiCollege of Information Science and Engineering, Northeastern University, Shenyang, Liaoning, 110819, China.
Linh V NguyenInstitute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
Kelly HillSouth Australian Research and Development Institute, Urrbrae, SA, 5064, Australia.
Heike Ebendorff-HeidepriemInstitute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
Erik P SchartnerInstitute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
Yong ZhaoCollege of Information Science and Engineering, Northeastern University, Shenyang, Liaoning, 110819, China.
Xue ZhouCollege of Information Science and Engineering, Northeastern University, Shenyang, Liaoning, 110819, China.
Yanan ZhangCollege of Information Science and Engineering, Northeastern University, Shenyang, Liaoning, 110819, China.
Stephen C Warren-SmithInstitute for Photonics and Advanced Sensing and School of Physical Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative polymerase chain reaction (qPCR), the real-time amplification and measurement of a targeted DNA molecule, has revolutionized the biological sciences and is routinely applied in areas such as medical diagnostics, forensics, and agriculture. Despite widescale use of qPCR technology in the lab, the availability of low-cost and high-speed portable systems remains one of the barriers to routine in-field implementation. Here we propose and demonstrate a potential solution using a photonics-based qPCR system. By using an all-optical approach, we achieve ultra-fast temperature response with real-time temperature feedback using nanoliter scale reaction volumes. The system uses a microcavity to act as a nanoliter scale reaction vessel with a laser-driven and optically monitored temperature cycling system for ultrafast thermal cycling and incorporates an all-fiber fluorescence excitation/detection system to achieve real-time, high sensitivity fluorescence monitoring of the qPCR process. Further, we demonstrate the potential of the system to operate as a label-free qPCR system through direct optical measurement of the sample refractive index. Due to advantages in portability and fabrication simplicity, we anticipate that this platform technology will offer a new strategy for fundamental techniques in biochemistry applications, such as point-of-care and remote diagnostics.

Indexed as

BiosensorDNA detectionLabel-freeMicrocavityOptical fiber sensorQuantitative polymerase chain reaction

Identifiers

PMID32834504
PMCPMC7415342

What OpenQuestion holds

Textmetadata
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.