Evidence map›Paper›PMID 23023004›Full record

ArticleGenetics2012

Local ancestry corrects for population structure in Saccharomyces cerevisiae genome-wide association studies.

Liyang Diao, Kevin C Chen

Erratum issuedAbstract read
In one paragraph

Article in Genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Extensive simulations assess the performance of genome-wide association mapping in variousPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors.

Liyang DiaoBioMaPS Institute for Quantitative Biology and Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Kevin C Chen

Funding

Genome-wide identification of cis-regulatory polymorphisms in S. cerevisiaeR00HG004515 · NHGRI · RUTGERS, THE STATE UNIV OF N.J. · PI CHEN, KEVIN · 2009 to 2011
$747k
NHGRI NIH HHS R00 HG004515NHGRI NIH HHS R00HG004515
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have become an important method for mapping the genetic loci underlying complex phenotypic traits in many species. A crucial issue when performing GWAS is to control for the underlying population structure because not doing so can lead to spurious associations. Population structure is a particularly important issue in nonhuman species since it is often difficult to control for population structure during the study design phase, requiring population structure to be corrected statistically after the data have been collected. It has not yet been established if GWAS is a feasible approach in Saccharomyces cerevisiae, an important model organism and agricultural species. We thus performed an empirical study of statistical methods for controlling for population structure in GWAS using a set of 201 phenotypic traits measured in multiple resequenced strains of S. cerevisiae. We complemented our analysis of real data with an extensive set of simulations. Our main result is that a mixed linear model using the local ancestry of the strain as a covariate is effective at controlling for population structure, consistent with the mosaic structure of many S. cerevisiae strains. We further studied the evolutionary forces acting on the GWAS SNPs and found that SNPs associated with variation in phenotypic traits are enriched for low minor allele frequencies, consistent with the action of negative selection on these SNPs. Despite the effectiveness of local ancestry correction, GWAS remains challenging in highly structured populations, such as S. cerevisiae. Nonetheless, we found that, even after correcting for population structure, there is still sufficient statistical power to recover biologically meaningful associations.

Indexed as

Genetics, PopulationGenome-Wide Association StudyModels, GeneticPolymorphism, Single NucleotideComputer SimulationGene FrequencyGenome, FungalLinear ModelsMathematical ComputingPhenotypeSaccharomyces cerevisiae

Identifiers

PMID23023004
PMCPMC3512155

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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.