Evidence map›Paper›PMID 27488097›Full record

ArticleGenetic epidemiology2016

Prioritizing individual genetic variants after kernel machine testing using variable selection.

Qianchuan He, Tianxi Cai, Yang Liu, Ni Zhao, Quaker E Harmon, Lynn M Almli, Elisabeth B Binder, Stephanie M Engel, Kerry J Ressler, Karen N Conneely and 2 more

Open access · greenAbstract read
In one paragraph

Article in Genetic epidemiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Leveraging human genetic and adverse outcome pathway (AOP) data to inform susceptibility in human health risk assessment.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    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

12 authors at 7 institutions in 2 countries.

Qianchuan HePublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Tianxi CaiDepartment of Biostatistics, Harvard School of Public Health, Boston, Massachusetts, United States of America.
Yang LiuPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Ni ZhaoPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Quaker E HarmonEpidemiology Branch, NIEHS, Research Triangle Park, North Carolina, United States of America.
Lynn M AlmliDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Elisabeth B BinderDepartment of Translational Research in Psychiatry, Max-Planck Institute of Psychiatry, Munich, Germany.
Stephanie M EngelDepartment of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Kerry J ResslerDivision of Depression & Anxiety Disorders, McLean Hospital, Belmont, Massachusetts, United States of America.
Karen N ConneelyDepartment of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Xihong LinDepartment of Biostatistics, Harvard School of Public Health, Boston, Massachusetts, United States of America.
Michael C WuPublic Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Fred Hutch Cancer Center · USEmory University · USHarvard University · USMax Planck Institute of Psychiatry · DEMcLean Hospital · USNational Institute of Environmental Health Sciences · USUniversity of North Carolina at Chapel Hill · US

Funding

Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI SUSAN A KORRICK · 1985 to 2026
$44.6M
TrainingU54HG007963 · NHGRI · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S., MURPHY, SHAWN N · 2014 to 2018
$18.3M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
Genetic and Trauma-Related Risk Factors for PTSDR01MH071537 · NIMH · EMORY UNIVERSITY · PI RESSLER, KERRY J. · 2005 to 2014
$8.5M
Statistical Methods for the Spatio-Temporal Assessment of Social Disparities in CancerP01CA134294 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANEUSE, SEBASTIEN, HERNAN, MIGUEL · 2008 to 2017
$6.8M
Genetic and estrogen-dependent regulation of the human PAC1R receptor and PTSDR01MH096764 · NIMH · MCLEAN HOSPITAL · PI RESSLER, KERRY J. · 2012 to 2016
$2.1M
Design and Analysis of Sequencing-based Studies for Complex Human TraitsR01HG006292 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, YUN · 2011 to 2015
$1.8M
Enhanced Gene Identification in Complex Traits Using Kernel MachinesR01HG007508 · NHGRI · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2013 to 2015
$1.0M
FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
Maternal Genetic Variation and Risk of Adverse Pregnancy OutcomesR21HD060207 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ENGEL, STEPHANIE · 2009 to 2010
$440k
NCI NIH HHS P01 CA134294NCI NIH HHS R35 CA197449NHGRI NIH HHS R01 HG006292NHGRI NIH HHS R01 HG007508NHGRI NIH HHS U54 HG007963NICHD NIH HHS R21 HD060207NIEHS NIH HHS P30 ES000002NIH HHS S10 OD020069NIMH NIH HHS R01 MH071537NIMH NIH HHS R01 MH096764
6 · The paper itself

Abstract

Kernel machine learning methods, such as the SNP-set kernel association test (SKAT), have been widely used to test associations between traits and genetic polymorphisms. In contrast to traditional single-SNP analysis methods, these methods are designed to examine the joint effect of a set of related SNPs (such as a group of SNPs within a gene or a pathway) and are able to identify sets of SNPs that are associated with the trait of interest. However, as with many multi-SNP testing approaches, kernel machine testing can draw conclusion only at the SNP-set level, and does not directly inform on which one(s) of the identified SNP set is actually driving the associations. A recently proposed procedure, KerNel Iterative Feature Extraction (KNIFE), provides a general framework for incorporating variable selection into kernel machine methods. In this article, we focus on quantitative traits and relatively common SNPs, and adapt the KNIFE procedure to genetic association studies and propose an approach to identify driver SNPs after the application of SKAT to gene set analysis. Our approach accommodates several kernels that are widely used in SNP analysis, such as the linear kernel and the Identity by State (IBS) kernel. The proposed approach provides practically useful utilities to prioritize SNPs, and fills the gap between SNP set analysis and biological functional studies. Both simulation studies and real data application are used to demonstrate the proposed approach.

Indexed as

Data Interpretation, StatisticalGenetic Association StudiesBirth WeightEndothelin-1Genetic MarkersHumansMethylenetetrahydrofolate Reductase (NADPH2)Models, GeneticPhenotypePolymorphism, Single NucleotideSelection, GeneticWounds and InjuriesEndothelin-1Genetic MarkersMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humangenetic association studieskernel machine methodsKNIFEset-basedvariable selection

Identifiers

PMID27488097
PMCPMC5118060
OpenAlexW2502222978

What OpenQuestion holds

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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.