Evidence map›Paper›PMID 29931045›Full record

ArticleBioinformatics (Oxford, England)2019

GWASinlps: non-local prior based iterative SNP selection tool for genome-wide association studies.

Nilotpal Sanyal, Min-Tzu Lo, Karolina Kauppi, Srdjan Djurovic, Ole A Andreassen, Valen E Johnson, Chi-Hua Chen

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  7. Bayesian GWAS with Structured and Non-Local Priors.Bioinformatics (Oxford, England) · 2020
    Article
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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

7 authors.

Nilotpal SanyalDepartment of Radiology, University of California, San Diego, La Jolla, CA, USA.
Min-Tzu LoDepartment of Radiology, University of California, San Diego, La Jolla, CA, USA.
Karolina KauppiDepartment of Radiation Sciences, Umeå University, Umeå, Sweden.
Srdjan DjurovicDepartment of Medical Genetics, NORMENT, KG Jebsen Centre, University of Bergen, Bergen, Oslo University Hospital, Oslo, Norway.
Ole A AndreassenDivision of Mental Health and Addiction, NORMENT, KG Jebsen Centre, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Valen E JohnsonDepartment of Statistics, Texas A&M University, College Station, TX, USA.
Chi-Hua ChenDepartment of Radiology, University of California, San Diego, La Jolla, CA, USA.

Funding

Consistent variable selection in p>>n settingsR01CA158113 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI JOHNSON, VALEN EARL · 2011 to 2020
$2.8M
Identifying the Polygenic Basis of the Human Brain and Psychiatric DisordersR01MH100351 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, CHI-HUA · 2013 to 2017
$2.1M
NCI NIH HHS R01 CA158113NIMH NIH HHS R01 MH100351
6 · The paper itself

Abstract

Motivation: Multiple marker analysis of the genome-wide association study (GWAS) data has gained ample attention in recent years. However, because of the ultra high-dimensionality of GWAS data, such analysis is challenging. Frequently used penalized regression methods often lead to large number of false positives, whereas Bayesian methods are computationally very expensive. Motivated to ameliorate these issues simultaneously, we consider the novel approach of using non-local priors in an iterative variable selection framework. Results: We develop a variable selection method, named, iterative non-local prior based selection for GWAS, or GWASinlps, that combines, in an iterative variable selection framework, the computational efficiency of the screen-and-select approach based on some association learning and the parsimonious uncertainty quantification provided by the use of non-local priors. The hallmark of our method is the introduction of 'structured screen-and-select' strategy, that considers hierarchical screening, which is not only based on response-predictor associations, but also based on response-response associations and concatenates variable selection within that hierarchy. Extensive simulation studies with single nucleotide polymorphisms having realistic linkage disequilibrium structures demonstrate the advantages of our computationally efficient method compared to several frequentist and Bayesian variable selection methods, in terms of true positive rate, false discovery rate, mean squared error and effect size estimation error. Further, we provide empirical power analysis useful for study design. Finally, a real GWAS data application was considered with human height as phenotype. Availability and implementation: An R-package for implementing the GWASinlps method is available at https://cran.r-project.org/web/packages/GWASinlps/index.html. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Genome-Wide Association StudyLinkage DisequilibriumPolymorphism, Single NucleotideSoftwareBayes TheoremComputational BiologyHumansRegression Analysis

Identifiers

PMID29931045
PMCPMC6298063

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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.