Evidence map›Paper›PMID 8421694›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Genome mapping by nonrandom anchoring: a discrete theoretical analysis.

M Q Zhang, T G Marr

Abstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. In vitro reconstruction of the Aspergillus (= Emericella) nidulans genome.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  7. 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

2 authors.

M Q ZhangCold Spring Harbor Laboratory, NY 11724.
T G Marr

Funding

FISSION YEAST GENOME MAPPINGR01HG000017 · NHGRI · COLD SPRING HARBOR LABORATORY · PI BEACH, DAVID H. · 1990 to 1992
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DATABASE AND COMPUTER TOOLS FOR GENOME MAPPINGR01HG000203 · NHGRI · COLD SPRING HARBOR LABORATORY · PI MARR, THOMAS G · 1991 to 1994
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NHGRI NIH HHS 1R01 HG00203-01A1NHGRI NIH HHS R01 HG00017-02
6 · The paper itself

Abstract

As part of our effort to construct a physical map of the genome of the fission yeast Schizosaccharomyces pombe, we have made theoretical predictions for the progress expected, as measured by the expected length fraction of island coverage and by the expected properties of the anchored islands such as the number and the size of islands. Our experimental strategy is to construct a random clone library and screen the library for clones having unique sequence at both ends. This scheme is essentially the same as the clone-limited double sequence-tagged-site selection scheme which was used in a computer simulation by Palazzolo et al. [Palazzolo, M. J., Sawyer, S. A., Martin, C. H., Smoller, D. A. & Hartl, D. L. (1991) Proc. Natl. Acad. Sci. USA 88, 8034-8038]. Both simulation and ongoing experiments in our laboratory have shown that the nonrandom anchoring method is far superior to random anchoring. In this paper, we propose a theoretical model to explain the simulated data and the experimental data.

Indexed as

Genome, FungalModels, GeneticSequence Tagged SitesChromosome MappingComputer SimulationGene LibrarySchizosaccharomyces

Identifiers

PMID8421694
PMCPMC45711

What OpenQuestion holds

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Read underepoch 390

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.