Evidence map›Paper›PMID 22042575›Full record

ArticleGenetics2012

Estimation of quantitative trait locus effects with epistasis by variational Bayes algorithms.

Zitong Li, Mikko J Sillanpää

Abstract 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. Cited by 21 papers.

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21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. An approximate Bayesian significance test for genomic evaluations.Biometrical journal. Biometrische Zeitschrift · 2018
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  10. Exploring the areas of applicability of whole-genome prediction methods for Asian rice (Oryza sativa L.).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2015
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Article
  18. Swift block-updating EM and pseudo-EM procedures for Bayesian shrinkage analysis of quantitative trait loci.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2012
    Article
  19. Article
  20. Overview of LASSO-related penalized regression methods for quantitative trait mapping and genomic selection.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2012
    Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Zitong LiDepartment of Mathematics and Statistics, University of Helsinki, Helsinki FIN-00014, Finland.
Mikko J Sillanpää

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bayesian hierarchical shrinkage methods have been widely used for quantitative trait locus mapping. From the computational perspective, the application of the Markov chain Monte Carlo (MCMC) method is not optimal for high-dimensional problems such as the ones arising in epistatic analysis. Maximum a posteriori (MAP) estimation can be a faster alternative, but it usually produces only point estimates without providing any measures of uncertainty (i.e., interval estimates). The variational Bayes method, stemming from the mean field theory in theoretical physics, is regarded as a compromise between MAP and MCMC estimation, which can be efficiently computed and produces the uncertainty measures of the estimates. Furthermore, variational Bayes methods can be regarded as the extension of traditional expectation-maximization (EM) algorithms and can be applied to a broader class of Bayesian models. Thus, the use of variational Bayes algorithms based on three hierarchical shrinkage models including Bayesian adaptive shrinkage, Bayesian LASSO, and extended Bayesian LASSO is proposed here. These methods performed generally well and were found to be highly competitive with their MCMC counterparts in our example analyses. The use of posterior credible intervals and permutation tests are considered for decision making between quantitative trait loci (QTL) and non-QTL. The performance of the presented models is also compared with R/qtlbim and R/BhGLM packages, using a previously studied simulated public epistatic data set.

Indexed as

Epistasis, GeneticQuantitative Trait LociAlgorithmsBayes TheoremComputer SimulationModels, Genetic

Identifiers

PMID22042575
PMCPMC3249367

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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.