Evidence map›Paper›PMID 2385591›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1990

Physical mapping of human chromosomes by repetitive sequence fingerprinting.

R L Stallings, D C Torney, C E Hildebrand, J L Longmire, L L Deaven, J H Jett, N A Doggett, R K Moyzis

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Article
  3. Chromosomes in the flow to simplify genome analysis.Functional & integrative genomics · 2012
    Review
  4. Non-B DNA structure-induced genetic instability and evolution.Cellular and molecular life sciences : CMLS · 2010
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Ordered restriction endonuclease maps of yeast artificial chromosomes created by optical mapping on surfaces.Proceedings of the National Academy of Sciences of the United States of America · 1995
    Article
  12. Article
  13. A mouse monochromosome 8 somatic cell hybrid: a reagent for chromosome 8 isolation.Mammalian genome : official journal of the International Mammalian Genome Society · 1994
    Article
  14. Article
  15. Review
  16. The human genome project.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Review
  17. Low-frequency chimeric yeast artificial chromosome libraries from flow-sorted human chromosomes 16 and 21.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  18. Genome mapping by nonrandom anchoring: a discrete theoretical analysis.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  19. Genome organization of repetitive elements in the rodent, Peromyscus leucopus.Mammalian genome : official journal of the International Mammalian Genome Society · 1993
    Article
  20. Definition, distribution, and use of a conserved Bovidae retroposon element sequence motif.Mammalian genome : official journal of the International Mammalian Genome Society · 1993
    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

8 authors.

R L StallingsCenter for Human Genome Studies, Los Alamos National Laboratory, University of California, NM 87545.
D C Torney
C E Hildebrand
J L Longmire
L L Deaven
J H Jett
N A Doggett
R K Moyzis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed an approach for identifying overlapping cosmid clones by exploiting the high density of repetitive sequences in complex genomes. Individual clones are fingerprinted, using a combination of restriction enzyme digestions followed by hybridization with selected classes of repetitive sequences. This "repeat fingerprinting" technique allows small regions of clone overlap (10-20%) to be unambiguously assigned. We demonstrate the utility of this approach, using the fingerprinting of 3145 cosmid clones (1.25 x coverage), containing one or more (GT)n repeats, from human chromosome 16. A statistical analysis was used to link these clones into 460 contiguous sequences (contigs), averaging 106 kilobases (kb) in length and representing approximately 54% (48.7 Mb) of the euchromatic arms of this chromosome. These values are consistent with theoretical calculations and indicate that 150- to 200-kb contigs can be generated with 1.5 x coverage. This strategy requires the fingerprinting of approximately one-fourth as many cosmids as random strategies requiring 50% minimum overlap for overlap detection. By "nucleating" at specific regions in the human genome, and exploiting the high density of interspersed sequences, this approach allows (i) the rapid generation of large (greater than 100-kb) contigs in the early stages of contig mapping and (ii) the production of a contig map with useful landmarks for rapid integration of the genetic and physical maps.

Indexed as

Chromosome MappingChromosomes, HumanRepetitive Sequences, Nucleic AcidChromosomes, Human, Pair 16Cloning, MolecularCosmidsDNADNA ProbesGene LibraryHumansNucleic Acid HybridizationNucleotide MappingRestriction MappingDNADNA Probes

Identifiers

PMID2385591
PMCPMC54504

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.