Evidence map›Paper›PMID 23071457›Full record

ArticlePLoS genetics2012

Use of pleiotropy to model genetic interactions in a population.

Gregory W Carter, Michelle Hays, Amir Sherman, Timothy Galitski

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014
    Review
  15. Article
  16. Article
  17. Dissection of complex gene expression using the combined analysis of pleiotropy and epistasis.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2014
    Article
  18. Article
  19. 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

4 authors at 2 institutions in 1 country.

Gregory W CarterThe Jackson Laboratory, Bar Harbor, Maine, USA. Greg.Carter@jax.org
Michelle Hays
Amir Sherman
Timothy Galitski
Institute for Systems Biology · USJackson Laboratory · US

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI GRABER, JOEL H · 2006 to 2015
$31.0M
Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
Inference and Testing of Quantitative Models of Genetic InteractionK25GM079404 · NIGMS · JACKSON LABORATORY · PI CARTER, GREGORY W · 2007 to 2011
$545k
NIGMS NIH HHS K25 GM079404NIGMS NIH HHS P50 GM076468NIGMS NIH HHS P50 GM076547
6 · The paper itself

Abstract

Systems-level genetic studies in humans and model systems increasingly involve both high-resolution genotyping and multi-dimensional quantitative phenotyping. We present a novel method to infer and interpret genetic interactions that exploits the complementary information in multiple phenotypes. We applied this approach to a population of yeast strains with randomly assorted perturbations of five genes involved in mating. We quantified pheromone response at the molecular level and overall mating efficiency. These phenotypes were jointly analyzed to derive a network of genetic interactions that mapped mating-pathway relationships. To determine the distinct biological processes driving the phenotypic complementarity, we analyzed patterns of gene expression to find that the pheromone response phenotype is specific to cellular fusion, whereas mating efficiency was a combined measure of cellular fusion, cell cycle arrest, and modifications in cellular metabolism. We applied our novel method to global gene expression patterns to derive an expression-specific interaction network and demonstrate applicability to global transcript data. Our approach provides a basis for interpretation of genetic interactions and the generation of specific hypotheses from populations assayed for multiple phenotypes.

Indexed as

Epistasis, GeneticGenetic PleiotropyModels, GeneticAlgorithmsGene Expression Regulation, FungalGene Regulatory NetworksMutationPhenotypeTranscription FactorsYeastsTranscription Factors

Identifiers

PMID23071457
PMCPMC3469415
OpenAlexW2086691364

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.