Evidence map›Paper›PMID 10606669›Full record

ArticleNucleic acids research2000

Cloning of polymorphisms (COP): enrichment of polymorphic sequences from complex genomes.

J Li, F Wang, V Zabarovska, C Wahlestedt, E R Zabarovsky

Abstract read
In one paragraph

Article in Nucleic acids research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

J LiCenter for Genomics Research, Karolinska Institute, 171 77 Stockholm, Sweden.
F Wang
V Zabarovska
C Wahlestedt
E R Zabarovsky

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we describe a new procedure (cloning of polymorphisms, COP) for enrichment of single nucleotide polymorphisms (SNPs) that represent restriction fragment length polymorphisms (RFLPs). COP would be applicable to the isolation of SNPs from particular regions of the genome, e.g. CpG islands, chromosomal bands, YACs or PAC contigs. A combination of digestion with restriction enzymes, treatment with uracil-DNA glycosylase and mung bean nuclease, PCR amplification and purification with streptavidin magnetic beads was used to isolate polymorphic sequences from the genomes of two human samples. After only two cycles of enrichment, 80% of the isolated clones were found to contain RFLPs. A simple method for the PCR detection of these polymorphisms was also developed.

Indexed as

DNA GlycosylasesPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideCloning, MolecularDNAElectrophoresis, Agar GelGenome, HumanHumansN-Glycosyl HydrolasesPolymerase Chain ReactionSingle-Strand Specific DNA and RNA EndonucleasesUracil-DNA GlycosidaseDNADNA GlycosylasesN-Glycosyl HydrolasesSingle-Strand Specific DNA and RNA EndonucleasesUracil-DNA Glycosidase

Identifiers

PMID10606669
PMCPMC102533

What OpenQuestion holds

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Registered trials

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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.