Evidence map›Paper›PMID 28832112›Full record

ArticleACS nano2017

Simultaneous Profiling of DNA Mutation and Methylation by Melting Analysis Using Magnetoresistive Biosensor Array.

Giovanni Rizzi, Jung-Rok Lee, Christina Dahl, Per Guldberg, Martin Dufva, Shan X Wang, Mikkel F Hansen

Abstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Giant Magnetoresistance Biosensors in Biomedical Applications.ACS applied materials & interfaces · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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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

7 authors.

Giovanni RizziDepartment of Micro- and Nanotechnology DTU Nanotech, Technical University of Denmark , Building 345B, Kongens Lyngby, DK 2800, Denmark.ORCID 0000-0003-3512-7389
Jung-Rok LeeDivision of Mechanical and Biomedical Engineering, ELTEC College of Engineering, Ewha Womans University , Seoul 03760, South Korea.
Christina DahlDanish Cancer Society Research Center , Copenhagen, DK 2100, Denmark.
Per GuldbergDanish Cancer Society Research Center , Copenhagen, DK 2100, Denmark.
Martin DufvaDepartment of Micro- and Nanotechnology DTU Nanotech, Technical University of Denmark , Building 345B, Kongens Lyngby, DK 2800, Denmark.
Shan X WangDepartment of Materials Science and Engineering, Stanford University , Stanford, California 93405, United States.
Mikkel F HansenDepartment of Micro- and Nanotechnology DTU Nanotech, Technical University of Denmark , Building 345B, Kongens Lyngby, DK 2800, Denmark.

Funding

Pilot ProjectsU54CA151459 · NCI · STANFORD UNIVERSITY · PI QUAKE, STEPHEN R · 2010 to 2014
$12.6M
Nano Characterization and Nano Fabrication CoreU54CA199075 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2015 to 2019
$9.6M
Ultra-Fast Epigenomic Maps for Monitoring AutoimmunityU19AI110491 · NIAID · STANFORD UNIVERSITY · PI UTZ, PAUL JOSEPH · 2014 to 2018
$3.6M
NCI NIH HHS U54 CA151459NCI NIH HHS U54 CA199075NIAID NIH HHS U19 AI110491
6 · The paper itself

Abstract

Epigenetic modifications, in particular DNA methylation, are gaining increasing interest as complementary information to DNA mutations for cancer diagnostics and prognostics. We introduce a method to simultaneously profile DNA mutation and methylation events for an array of sites with single site specificity. Genomic (mutation) or bisulphite-treated (methylation) DNA is amplified using nondiscriminatory primers, and the amplicons are then hybridized to a giant magnetoresistive (GMR) biosensor array followed by melting curve measurements. The GMR biosensor platform offers scalable multiplexed detection of DNA hybridization, which is insensitive to temperature variation. The melting curve approach further enhances the assay specificity and tolerance to variations in probe length. We demonstrate the utility of this method by simultaneously profiling five mutation and four methylation sites in human melanoma cell lines. The method correctly identified all mutation and methylation events and further provided quantitative assessment of methylation density validated by bisulphite pyrosequencing.

Indexed as

Biosensing TechniquesCell Line, TumorDNADNA MethylationDNA Mutational AnalysisEquipment DesignHumansMelanomaMutationNucleic Acid DenaturationOligonucleotide Array Sequence AnalysisDNADNA arrayGMR biosensormelanomamelting curvemethylationmutation

Identifiers

PMID28832112
PMCPMC5810360

What OpenQuestion holds

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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.