Evidence map›Paper›PMID 19199618›Full record

ArticleJournal of the American Chemical Society2009

Surface-enhanced Raman scattering based ligase detection reaction.

Yun Suk Huh, Adam J Lowe, Aaron D Strickland, Carl A Batt, David Erickson

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 90 citations in OpenAlex.

  1. Fluorescence-Based Detection ofMethods and protocols · 2025
    Article
  2. Article
  3. Single-Step FRET-Based Detection of Femtomoles DNA.Sensors (Basel, Switzerland) · 2019
    Article
  4. Article
  5. Article
  6. Single Nucleotide Polymorphism Genotyping in Single-Molecule Electronic Circuits.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2017
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. A method for nanofluidic device prototyping using elastomeric collapse.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
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

5 authors at 1 institution in 1 country.

Yun Suk HuhSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, New York 14853, USA.
Adam J Lowe
Aaron D Strickland
Carl A Batt
David Erickson
Cornell University · US

Funding

Nanoscale Optofluidic Pathogen DetectionR21EB007031 · NIBIB · CORNELL UNIVERSITY · PI ERICKSON, DAVID CARL · 2007 to 2009
$554k
NIBIB NIH HHS R21 EB007031NIBIB NIH HHS R21EB007031
6 · The paper itself

Abstract

Genomics provides a comprehensive view of the complete genetic makeup of an organism. Individual sequence variations, as manifested by single nucleotide polymorphisms (SNPs), can provide insight into the basis for a large number of phenotypes and diseases including cancer. The ability rapidly screen for SNPs will have a profound impact on a number of applications, most notably personalized medicine. Here we demonstrate a new approach to SNP detection through the application of surface-enhanced Raman scattering (SERS) to the ligase detection reaction (LDR). The reaction uses two LDR primers, one of which contains a Raman enhancer and the other a reporter dye. In LDR, one of the primers is designed to interrogate the SNP. When the SNP being interrogated matches the discriminating primer sequence, the primers are ligated and the enhancer and dye are brought into close proximity enabling the dye's Raman signature to be detected. By detecting the Raman signature of the dye rather than its fluorescence emission, our technique avoids the problem of spectral overlap which limits number of reactions which can be carried out in parallel by existing systems. We demonstrate the LDR-SERS reaction for the detection of point mutations in the human K-ras oncogene. The reaction is implemented in an electrokinetically active microfluidic device that enables physical concentration of the reaction products for enhanced detection sensitivity and quantization. We report a limit of detection of 20 pM of target DNA with the anticipated specificity engendered by the LDR platform.

Indexed as

Polymorphism, Single NucleotideDNADNA Mutational AnalysisGenes, rasHumansLigase Chain ReactionModels, MolecularPoint MutationSpectrum Analysis, RamanDNA

Identifiers

PMID19199618
PMCPMC2716065
OpenAlexW1964650835

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.