Evidence map›Paper›PMID 31010934›Full record

ArticleGenetics2019

Structured Genome-Wide Association Studies with Bayesian Hierarchical Variable Selection.

Yize Zhao, Hongtu Zhu, Zhaohua Lu, Rebecca C Knickmeyer, Fei Zou

Abstract read
In one paragraph

Article in Genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Genetic underpinnings of brain structural connectome for young adults.Journal of the American Statistical Association · 2023
    Article
  4. Genome-Wide Association Study Statistical Models: A Review.Methods in molecular biology (Clifton, N.J.) · 2022
    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

5 authors.

Yize ZhaoDepartment of Healthcare Policy and Research, Cornell University Weill Cornell, New York, New York 10065 yiz2013@med.cornell.edu.ORCID 0000-0001-6283-2302
Hongtu ZhuDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina 27599.
Zhaohua LuDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee 38105.
Rebecca C KnickmeyerDepartment of Pediatrics and Human Development, Michigan State University, East Lansing, Michigan 48824.
Fei ZouDepartment of Biostatistics, University of Florida, Gainesville, Florida 32611.

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
NIEHS NIH HHS P30 ES010126
6 · The paper itself

Abstract

It becomes increasingly important in using genome-wide association studies (GWAS) to select important genetic information associated with qualitative or quantitative traits. Currently, the discovery of biological association among SNPs motivates various strategies to construct SNP-sets along the genome and to incorporate such set information into selection procedure for a higher selection power, while facilitating more biologically meaningful results. The aim of this paper is to propose a novel Bayesian framework for hierarchical variable selection at both SNP-set (group) level and SNP (within group) level. We overcome a key limitation of existing posterior updating scheme in most Bayesian variable selection methods by proposing a novel sampling scheme to explicitly accommodate the ultrahigh-dimensionality of genetic data. Specifically, by constructing an auxiliary variable selection model under SNP-set level, the new procedure utilizes the posterior samples of the auxiliary model to subsequently guide the posterior inference for the targeted hierarchical selection model. We apply the proposed method to a variety of simulation studies and show that our method is computationally efficient and achieves substantially better performance than competing approaches in both SNP-set and SNP selection. Applying the method to the Alzheimers Disease Neuroimaging Initiative (ADNI) data, we identify biologically meaningful genetic factors under several neuroimaging volumetric phenotypes. Our method is general and readily to be applied to a wide range of biomedical studies.

Indexed as

Computer SimulationAlgorithmsAlzheimer DiseaseBayes TheoremGenetic MarkersGenome-Wide Association StudyHumansMarkov ChainsModels, GeneticNeuroimagingPhenotypePolymorphism, Single NucleotideGenetic MarkersBayesian variable selectiongenome-wide association studiesimaging geneticsMarkov chain Monte CarloSNP-set

Identifiers

PMID31010934
PMCPMC6553832

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.