Evidence map›Paper›PMID 23466369›Full record

ArticleHuman heredity2012

A novel kernel for correcting size bias in the logistic kernel machine test with an application to rheumatoid arthritis.

Saskia Freytag, Heike Bickeböller, Christopher I Amos, Thomas Kneib, Martin Schlather

Abstract read
In one paragraph

Article in Human heredity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies.Computational and mathematical methods in medicine · 2017
    Article
  4. Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Saskia FreytagDepartment of Genetic Epidemiology, Medical School, Georg-August University Göttingen, Göttingen, Germany. saskia.freytag@med.uni-goettingen.de
Heike Bickeböller
Christopher I Amos
Thomas Kneib
Martin Schlather

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
NARAC The Genetics of Rheumatoid ArthritisR01AR044422 · NIAMS · NORTH SHORE UNIVERSITY HOSPITAL · PI GREGERSEN, PETER K. · 1997 to 2011
$6.0M
NCI NIH HHS P30 CA023108NIAMS NIH HHS AR44422NIAMS NIH HHS R01 AR044422
6 · The paper itself

Abstract

objectivesThe logistic kernel machine test (LKMT) is a testing procedure tailored towards high-dimensional genetic data. Its use in pathway analyses of case-control genome-wide association studies results from its computational efficiency and flexibility in incorporating additional information via the kernel. The kernel can be any positive definite function; unfortunately, its form strongly influences the test's power and bias. Most authors have recommended the use of a simple linear kernel. We demonstrate via a simulation that the probability of rejecting the null hypothesis of no association just by chance increases with the number of SNPs or genes in the pathway when applying a simple linear kernel.

methodsWe propose a novel kernel that includes an appropriate standardization in order to protect against any inflation of false positive results. Moreover, our novel kernel contains information on gene membership of SNPs in the pathway.

resultsWhen applying the novel kernel to data from the North American Rheumatoid Arthritis Consortium, we find that even this basic genomic structure can improve the ability of the LKMT to identify meaningful associations. We also demonstrate that the standardization effectively eliminates problems of size bias.

conclusionWe recommend the use of our standardized kernel and urge caution when using non-adjusted kernels in the LKMT to conduct pathway analyses.

Indexed as

Models, GeneticArthritis, RheumatoidBiasComputer SimulationGenesGenome-Wide Association StudyHumansPolymorphism, Single NucleotideSample Size

Identifiers

PMID23466369
PMCPMC3779069

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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.