Evidence map›Paper›PMID 29041917›Full record

ArticleGenetics, selection, evolution : GSE2017

Locally epistatic models for genome-wide prediction and association by importance sampling.

Deniz Akdemir, Jean-Luc Jannink, Julio Isidro-Sánchez

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
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  7. Simultaneous selection for grain yield and protein content in genomics-assisted wheat breeding.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Non-additive Effects in Genomic Selection.Frontiers in genetics · 2018
    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

3 authors.

Deniz AkdemirStatGen Consulting, Ithaca, NY, USA. akdemir@statgenconsulting.com.
Jean-Luc JanninkRobert W. Holley Center for Agriculture and Health, USDA-ARS, Ithaca, NY, USA.
Julio Isidro-SánchezDepartment of Animal and Crop Science, University College Dublin, Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn statistical genetics, an important task involves building predictive models of the genotype-phenotype relationship to attribute a proportion of the total phenotypic variance to the variation in genotypes. Many models have been proposed to incorporate additive genetic effects into prediction or association models. Currently, there is a scarcity of models that can adequately account for gene by gene or other forms of genetic interactions, and there is an increased interest in using marker annotations in genome-wide prediction and association analyses. In this paper, we discuss a hybrid modeling method which combines parametric mixed modeling and non-parametric rule ensembles.

resultsThis approach gives us a flexible class of models that can be used to capture additive, locally epistatic genetic effects, gene-by-background interactions and allows us to incorporate one or more annotations into the genomic selection or association models. We use benchmark datasets that cover a range of organisms and traits in addition to simulated datasets to illustrate the strengths of this approach.

conclusionsIn this paper, we describe a new strategy for incorporating genetic interactions into genomic prediction and association models. This strategy results in accurate models, with sometimes significantly higher accuracies than that of a standard additive model.

Indexed as

AlgorithmsEpistasis, GeneticModels, GeneticAnimalsGenome-Wide Association StudyMiceOryzaTriticumZea mays

Identifiers

PMID29041917
PMCPMC5646165

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LicenceCC BY
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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.