Evidence map›Paper›PMID 17170132›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Four-color DNA sequencing by synthesis using cleavable fluorescent nucleotide reversible terminators.

Jingyue Ju, Dae Hyun Kim, Lanrong Bi, Qinglin Meng, Xiaopeng Bai, Zengmin Li, Xiaoxu Li, Mong Sano Marma, Shundi Shi, Jian Wu and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

76 citing papers in PubMed, 194 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Fluorophore-mediated Photooxidation of the Guanine Heterocycle.Journal of physical organic chemistry · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Genome sequencing guide: An introductory toolbox to whole-genome analysis methods.Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology · 2021
    Review
  17. Review
  18. Article
  19. Review
  20. Nucleotide analogues as inhibitors of SARS-CoV Polymerase.Pharmacology research & perspectives · 2020
    Article

16 more citing papers are in PubMed but not listed here.

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

13 authors at 1 institution in 1 country.

Jingyue JuColumbia Genome Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA. ju@c2b2.columbia.edu
Dae Hyun Kim
Lanrong Bi
Qinglin Meng
Xiaopeng Bai
Zengmin Li
Xiaoxu Li
Mong Sano Marma
Shundi Shi
Jian Wu
John R Edwards
Aireen Romu
Nicholas J Turro
Columbia University · US

Funding

Genomic Approaches to Neuronal Diversity and PlasticityP50HG002806 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JU, JINGYUE · 2003 to 2007
$13.9M
An Integrated System for DNA Sequencing by SynthesisR01HG003582 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2004 to 2009
$4.3M
NHGRI NIH HHS P50 HG002806NHGRI NIH HHS R01 HG003582
6 · The paper itself

Abstract

DNA sequencing by synthesis (SBS) on a solid surface during polymerase reaction offers a paradigm to decipher DNA sequences. We report here the construction of such a DNA sequencing system using molecular engineering approaches. In this approach, four nucleotides (A, C, G, T) are modified as reversible terminators by attaching a cleavable fluorophore to the base and capping the 3'-OH group with a small chemically reversible moiety so that they are still recognized by DNA polymerase as substrates. We found that an allyl moiety can be used successfully as a linker to tether a fluorophore to 3'-O-allyl-modified nucleotides, forming chemically cleavable fluorescent nucleotide reversible terminators, 3'-O-allyl-dNTPs-allyl-fluorophore, for application in SBS. The fluorophore and the 3'-O-allyl group on a DNA extension product, which is generated by incorporating 3'-O-allyl-dNTPs-allyl-fluorophore in a polymerase reaction, are removed simultaneously in 30 s by Pd-catalyzed deallylation in aqueous buffer solution. This one-step dual-deallylation reaction thus allows the reinitiation of the polymerase reaction and increases the SBS efficiency. DNA templates consisting of homopolymer regions were accurately sequenced by using this class of fluorescent nucleotide analogues on a DNA chip and a four-color fluorescent scanner.

Indexed as

Base SequenceColorDNAFluorescent DyesMolecular StructureNucleotidesOligonucleotide Array Sequence AnalysisSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationDNAFluorescent DyesNucleotides

Identifiers

PMID17170132
PMCPMC1702316
OpenAlexW4254945764

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.