Evidence map›Paper›PMID 21871061›Full record

ArticleBMC genetics2011

Gene- or region-based association study via kernel principal component analysis.

Qingsong Gao, Yungang He, Zhongshang Yuan, Jinghua Zhao, Bingbing Zhang, Fuzhong Xue

Abstract read
In one paragraph

Article in BMC genetics, 2011. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Gene-based mediation analysis in epigenetic studies.Briefings in bioinformatics · 2021
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Qingsong GaoDepartment of Epidemiology and Health Statistics, School of Public Health, Shandong University, Jinan 250012, China.
Yungang He
Zhongshang Yuan
Jinghua Zhao
Bingbing Zhang
Fuzhong Xue

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn genetic association study, especially in GWAS, gene- or region-based methods have been more popular to detect the association between multiple SNPs and diseases (or traits). Kernel principal component analysis combined with logistic regression test (KPCA-LRT) has been successfully used in classifying gene expression data. Nevertheless, the purpose of association study is to detect the correlation between genetic variations and disease rather than to classify the sample, and the genomic data is categorical rather than numerical. Recently, although the kernel-based logistic regression model in association study has been proposed by projecting the nonlinear original SNPs data into a linear feature space, it is still impacted by multicolinearity between the projections, which may lead to loss of power. We, therefore, proposed a KPCA-LRT model to avoid the multicolinearity.

resultsSimulation results showed that KPCA-LRT was always more powerful than principal component analysis combined with logistic regression test (PCA-LRT) at different sample sizes, different significant levels and different relative risks, especially at the genewide level (1E-5) and lower relative risks (RR = 1.2, 1.3). Application to the four gene regions of rheumatoid arthritis (RA) data from Genetic Analysis Workshop16 (GAW16) indicated that KPCA-LRT had better performance than single-locus test and PCA-LRT.

conclusionsKPCA-LRT is a valid and powerful gene- or region-based method for the analysis of GWAS data set, especially under lower relative risks and lower significant levels.

Indexed as

Genetic Association StudiesLogistic ModelsPrincipal Component AnalysisAlgorithmsComputer SimulationGenetic Predisposition to DiseaseHumansModels, StatisticalPolymorphism, Single Nucleotide

Identifiers

PMID21871061
PMCPMC3176196

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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.