Evidence map›Paper›PMID 27032065›Full record

ReviewCurrent opinion in biotechnology2016

Microfluidic techniques for high throughput single cell analysis.

Amy Reece, Bingzhao Xia, Zhongliang Jiang, Benjamin Noren, Ralph McBride, John Oakey

Abstract readReview
In one paragraph

Review in Current opinion in biotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Single-cell RNA sequencing offers novel perspectives in viral infection research.Frontiers in cellular and infection microbiology · 2026
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Bacteriuria and phenotypic antimicrobial susceptibility testing in 45 min by point-of-care Sysmex PA-100 System: first clinical evaluation.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
  9. Article
  10. Review
  11. Article
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  15. 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

6 authors.

Amy ReeceDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States.
Bingzhao XiaDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States.
Zhongliang JiangDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States.
Benjamin NorenDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States.
Ralph McBrideDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States.
John OakeyDepartment of Chemical Engineering, University of Wyoming, 1000 East University Avenue, Laramie, WY 82070, United States. Electronic address: joakey@uwyo.edu.

Funding

Wyoming INBRE Phase 4- Equipment Supplement for x-ray diffractometer for Center for Advanced Scientific InstrumentationP20GM103432 · NIGMS · UNIVERSITY OF WYOMING · PI Robert Scott Seville · 2012 to 2026
$56.8M
NIGMS NIH HHS P20 GM103432
6 · The paper itself

Abstract

The microfabrication of microfluidic control systems and the development of increasingly sensitive molecular amplification tools have enabled the miniaturization of single cells analytical platforms. Only recently has the throughput of these platforms increased to a level at which populations can be screened at the single cell level. Techniques based upon both active and passive manipulation are now capable of discriminating between single cell phenotypes for sorting, diagnostic or prognostic applications in a variety of clinical scenarios. The introduction of multiphase microfluidics enables the segmentation of single cells into biochemically discrete picoliter environments. The combination of these techniques are enabling a class of single cell analytical platforms within great potential for data driven biomedicine, genomics and transcriptomics.

Indexed as

High-Throughput Screening AssaysAnimalsHumansMicrofluidic Analytical TechniquesSingle-Cell Analysis

Identifiers

PMID27032065
PMCPMC4975615

What OpenQuestion holds

Textmetadata
LicenceTDM
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.