Evidence map›Paper›PMID 11691941›Full record

ArticleNucleic acids research2001

DNA sequencing using biotinylated dideoxynucleotides and mass spectrometry.

J R Edwards, Y Itagaki, J Ju

Abstract read
In one paragraph

Article in Nucleic acids research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. 3'-O-modified nucleotides as reversible terminators for pyrosequencing.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  4. Four-color DNA sequencing by synthesis using cleavable fluorescent nucleotide reversible terminators.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  5. Article
  6. Four-color DNA sequencing by synthesis on a chip using photocleavable fluorescent nucleotides.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  7. Article
  8. Photocleavable fluorescent nucleotides for DNA sequencing on a chip constructed by site-specific coupling chemistry.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  9. Article
  10. Article
  11. Article
  12. Photocleavage of a 2-nitrobenzyl linker bridging a fluorophore to the 5' end of DNA.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  13. A photocleavable fluorescent nucleotide for DNA sequencing and analysis.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  14. Article
  15. 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

3 authors.

J R EdwardsLaboratory of DNA Sequencing and Chemical Biology, Columbia Genome Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Y Itagaki
J Ju

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MS) has been explored widely for DNA sequencing. The major requirement for this method is that the DNA sequencing fragments must be free from alkaline and alkaline earth salts as well as other contaminants for accurately measuring the masses of the DNA fragments. We report here the development of a novel MS DNA sequencing method that generates Sanger-sequencing fragments in one tube using biotinylated dideoxynucleotides. The DNA sequencing fragments that carry a biotin at the 3'-end are made free from salts and other components in the sequencing reaction by capture with streptavidin-coated magnetic beads. Only correctly terminated biotinylated DNA fragments are subsequently released and loaded onto a mass spectrometer to obtain accurate DNA sequencing data. Compared with gel electrophoresis-based sequencing systems, MS produces a very high resolution of DNA-sequencing fragments, fast separation on microsecond time scales, and completely eliminates the compressions associated with gel electrophoresis. The high resolution of MS allows accurate mutation and heterozygote detection. This optimized solid-phase DNA-sequencing chemistry plus future improvements in detector sensitivity for large DNA fragments in MS instrumentation will further improve MS for DNA sequencing.

Indexed as

BiotinylationSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBase SequenceBiotinDideoxynucleosidesDNAHeterozygoteMicrospheresMolecular Sequence DataMutationPolymorphism, GeneticSensitivity and SpecificitySequence Analysis, DNAStreptavidinTemplates, GeneticBiotinDideoxynucleosidesDNAStreptavidin

Identifiers

PMID11691941
PMCPMC60203

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.