Evidence map›Paper›PMID 16339379›Full record

ArticleGenome research2005

Selective sweep mapping of genes with large phenotypic effects.

John P Pollinger, Carlos D Bustamante, Adi Fledel-Alon, Sheila Schmutz, Melissa M Gray, Robert K Wayne

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Article
  3. The Shape of the Nasal Cavity and Adaptations to Sniffing in the Dog (Animals : an open access journal from MDPI · 2022
    Review
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  14. Review
  15. A genetic assessment of the English bulldog.Canine genetics and epidemiology · 2016
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

6 authors at 3 institutions in 2 countries.

John P PollingerDepartment of Ecology and Evolutionary Biology, University of California, Los Angeles, California 90095-1606, USA. jpolling@ucla.edu
Carlos D Bustamante
Adi Fledel-Alon
Sheila Schmutz
Melissa M Gray
Robert K Wayne
University of California, Los Angeles · USCornell University · USUniversity of Saskatchewan · CA

Funding

Population Genetic Inferences From Dense Genotype DataR01HG003229 · NHGRI · CORNELL UNIVERSITY ITHACA · PI BUSTAMANTE, CARLOS DANIEL, CLARK, ANDREW G · 2004 to 2013
$4.8M
NHGRI NIH HHS 1R01HG003229-01NHGRI NIH HHS R01 HG003229
6 · The paper itself

Abstract

Many domestic dog breeds have originated through fixation of discrete mutations by intense artificial selection. As a result of this process, markers in the proximity of genes influencing breed-defining traits will have reduced variation (a selective sweep) and will show divergence in allele frequency. Consequently, low-resolution genomic scans can potentially be used to identify regions containing genes that have a major influence on breed-defining traits. We model the process of breed formation and show that the probability of two or three adjacent marker loci showing a spurious signal of selection within at least one breed (i.e., Type I error or false-positive rate) is low if highly variable and moderately spaced markers are utilized. We also use simulations with selection to demonstrate that even a moderately spaced set of highly polymorphic markers (e.g., one every 0.8 cM) has high power to detect regions targeted by strong artificial selection in dogs. Further, we show that a gene responsible for black coat color in the Large Munsterlander has a 40-Mb region surrounding the gene that is very low in heterozygosity for microsatellite markers. Similarly, we survey 302 microsatellite markers in the Dachshund and find three linked monomorphic microsatellite markers all within a 10-Mb region on chromosome 3. This region contains the FGFR3 gene, which is responsible for achondroplasia in humans, but not in dogs. Consequently, our results suggest that the causative mutation is a gene or regulatory region closely linked to FGFR3.

Indexed as

AnimalsBreedingChromosome MappingComputer SimulationDogsFemaleGenetic MarkersGenetic VariationGenomeHeterozygoteMaleModels, GeneticMutationPhenotypePolymorphism, GeneticReceptor, Fibroblast Growth Factor, Type 3Genetic MarkersReceptor, Fibroblast Growth Factor, Type 3

Identifiers

PMID16339379
PMCPMC1356119
OpenAlexW2109085179

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.