Evidence map›Paper›PMID 26594354›Full record

ArticleRSC advances2014

A Microfluidic Device for Multiplex Single-Nucleotide Polymorphism Genotyping.

Jing Zhu, Chunmei Qiu, Mirkó Palla, ThaiHuu Nguyen, James J Russo, Jingyue Ju, Qiao Lin

Open access · greenAbstract read
In one paragraph

Article in RSC advances, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 1 institution in 1 country.

Jing ZhuDepartment of Mechanical Engineering, Columbia University, New York, NY, 10027.
Chunmei QiuDepartment of Chemical Engineering, Columbia University, New York, NY, 10027.
Mirkó PallaDepartment of Mechanical Engineering, Columbia University, New York, NY, 10027 ; Department of Chemical Engineering, Columbia University, New York, NY, 10027.
ThaiHuu NguyenDepartment of Mechanical Engineering, Columbia University, New York, NY, 10027.
James J RussoDepartment of Chemical Engineering, Columbia University, New York, NY, 10027.
Jingyue JuDepartment of Chemical Engineering, Columbia University, New York, NY, 10027.
Qiao LinDepartment of Mechanical Engineering, Columbia University, New York, NY, 10027.
Columbia University · US

Funding

Molecular Engineering Approach to Study Long Term Synaptic PlasticityR01NS060762 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2008 to 2011
$2.3M
Theranostic Molecular Automata for Specific Cell EliminationRC2CA147925 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STOJANOVIC, MILAN N · 2009 to 2010
$1.8M
DNA Sequencing with Reversible dNTP and Cleavable Fluorescent ddNTPTerminatorsR01HG004774 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2008 to 2009
$946k
Microfluidic Selection of Aptamers for Biological Purification ApplicationsR21RR025816 · NCRR · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LIN, QIAO · 2010 to 2011
$392k
NCI NIH HHS RC2 CA147925NCRR NIH HHS R21 RR025816NHGRI NIH HHS R01 HG004774NINDS NIH HHS R01 NS060762
6 · The paper itself

Abstract

Single-nucleotide polymorphisms (SNPs) are the most abundant type of genetic variations; they provide the genetic fingerprint of individuals and are essential for genetic biomarker discoveries. Accurate detection of SNPs is of great significance for disease prevention, diagnosis and prognosis, and for prediction of drug response and clinical outcomes in patients. Nevertheless, conventional SNP genotyping methods are still limited by insufficient accuracy or labor-, time-, and resource-intensive procedures. Microfluidics has been increasingly utilized to improve efficiency; however, the currently available microfluidic genotyping systems still have shortcomings in accuracy, sensitivity, throughput and multiplexing capability. To address these challenges, we developed a multi-step SNP genotyping microfluidic device, which performs single-base extension of SNP specific primers and solid-phase purification of the extension products on a temperature-controlled chip. The products are ready for immediate detection by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), providing identification of the alleles at the target loci. The integrated device enables efficient and automated operation, while maintaining the high accuracy and sensitivity provided by MS. The multiplex genotyping capability was validated by performing rapid, accurate and simultaneous detection of 4 loci on a synthetic template. The microfluidic device has the potential to perform automatic, accurate, quantitative and high-throughput assays covering a broad spectrum of applications in biological and clinical research, drug development and forensics.

Indexed as

GenotypingMALDI-TOF MSMicrofluidicsSingle-Base Extension (SBE)Single-Nucleotide Polymorphism (SNP)Solid-Phase Purification (SPP)

Identifiers

PMID26594354
PMCPMC4651459
OpenAlexW2083428561

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.