Evidence map›Paper›PMID 15459281›Full record

ArticleNucleic acids research2004

Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR.

Brooks E Miner, Reinhard J Stöger, Alice F Burden, Charles D Laird, R Scott Hansen

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
  2. Methods to improve the accuracy of next-generation sequencing.Frontiers in bioengineering and biotechnology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The Pipeline Repertoire for Ig-Seq Analysis.Frontiers in immunology · 2019
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. How to deduplicate PCR.Nature methods · 2017
    Article
  19. Article
  20. 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.

Brooks E MinerDepartment of Biology, University of Washington, Seattle, WA 98195, USA. miner@u.washington.edu
Reinhard J Stöger
Alice F Burden
Charles D Laird
R Scott Hansen

Funding

Restoring FMRP Phenotypes Frpm Temporal Regional and Splice- Isoforms VarationsP30HD002274 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 1985 to 2013
$33.6M
DOSAGE COMPENSATION IN MAMMALS: X-INACTIVATIONR01HD016659 · NICHD · UNIVERSITY OF WASHINGTON · PI GARTLER, STANLEY · 1996 to 2004
$1.9M
MOLECULAR GENETICS AND EPIGENETICS OF FRAGILE X SYNDROMER01GM053805 · NIGMS · UNIVERSITY OF WASHINGTON · PI LAIRD, CHARLES D · 1995 to 2004
$918k
DOSAGE COMPENSATION IN MAMMALS: X-INACTIVATIONR37HD016659 · NICHD · UNIVERSITY OF WASHINGTON · PI GARTLER, STANLEY · 1986 to 1995
–
NICHD NIH HHS HD 02274NICHD NIH HHS HD 16659NICHD NIH HHS P30 HD002274NICHD NIH HHS R01 HD016659NIGMS NIH HHS GM 53805NIGMS NIH HHS R01 GM053805
6 · The paper itself

Abstract

PCR amplification of limited amounts of DNA template carries an increased risk of product redundancy and contamination. We use molecular barcoding to label each genomic DNA template with an individual sequence tag prior to PCR amplification. In addition, we include molecular 'batch-stamps' that effectively label each genomic template with a sample ID and analysis date. This highly sensitive method identifies redundant and contaminant sequences and serves as a reliable method for positive identification of desired sequences; we can therefore capture accurately the genomic template diversity in the sample analyzed. Although our application described here involves the use of hairpin-bisulfite PCR for amplification of double-stranded DNA, the method can readily be adapted to single-strand PCR. Useful applications will include analyses of limited template DNA for biomedical, ancient DNA and forensic purposes.

Indexed as

Base SequenceFragile X Messenger Ribonucleoprotein 1Genome, HumanHumansMaleMolecular Sequence DataNerve Tissue ProteinsPolymerase Chain ReactionPromoter Regions, GeneticRNA-Binding ProteinsSequence Analysis, DNASulfitesTemplates, GeneticFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Nerve Tissue ProteinsRNA-Binding ProteinsSulfites

Identifiers

PMID15459281
PMCPMC521679

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.