Literature DB >> 26111731

Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability.

Jin J Zhou1, Michael H Cho, Christoph Lange, Sharon Lutz, Edwin K Silverman, Nan M Laird.   

Abstract

Many correlated disease variables are analyzed jointly in genetic studies in the hope of increasing power to detect causal genetic variants. One approach involves assessing the relationship between each phenotype and each SNP individually and using a Bonferroni correction for the effective number of tests conducted. Alternatively, one can apply a multivariate regression or a dimension reduction technique, such as principal component analysis, and test for the association with the principal components of the phenotypes rather than the individual phenotypes. Inspired by the previous approaches of combining phenotypes to maximize heritability at individual SNPs, in this paper, we propose to construct a maximally heritable (MaxH) phenotype by taking advantage of the estimated total heritability and co-heritability. The heritability and co-heritability only need to be estimated once; therefore, our method is applicable to genome-wide scans. The MaxH phenotype is a linear combination of the individual phenotypes with increased heritability and power over the phenotypes being combined. Simulations show that the heritability and power achieved agree well with the theory for large samples and two phenotypes. We compare our approach with commonly used methods and assess both the heritability and the power of the MaxH phenotype. Moreover, we provide suggestions for how to choose the phenotypes for combination. An application of our approach to a GWAS on chronic obstructive pulmonary disease shows its practical relevance.
© 2015 S. Karger AG, Basel.

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Mesh:

Year:  2015        PMID: 26111731      PMCID: PMC4508328          DOI: 10.1159/000381641

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  33 in total

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10.  MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS.

Authors:  Paul F O'Reilly; Clive J Hoggart; Yotsawat Pomyen; Federico C F Calboli; Paul Elliott; Marjo-Riitta Jarvelin; Lachlan J M Coin
Journal:  PLoS One       Date:  2012-05-02       Impact factor: 3.240

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  9 in total

1.  Assessing pleiotropy and mediation in genetic loci associated with chronic obstructive pulmonary disease.

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Review 3.  Genetic Advances in Chronic Obstructive Pulmonary Disease. Insights from COPDGene.

Authors:  Margaret F Ragland; Christopher J Benway; Sharon M Lutz; Russell P Bowler; Julian Hecker; John E Hokanson; James D Crapo; Peter J Castaldi; Dawn L DeMeo; Craig P Hersh; Brian D Hobbs; Christoph Lange; Terri H Beaty; Michael H Cho; Edwin K Silverman
Journal:  Am J Respir Crit Care Med       Date:  2019-09-15       Impact factor: 21.405

4.  Joint analysis of multiple phenotypes using a clustering linear combination method based on hierarchical clustering.

Authors:  Xueling Li; Shuanglin Zhang; Qiuying Sha
Journal:  Genet Epidemiol       Date:  2019-09-20       Impact factor: 2.135

5.  Imputing Phenotypes for Genome-wide Association Studies.

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6.  Joint analysis of multiple phenotypes in association studies using allele-based clustering approach for non-normal distributions.

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8.  Joint Analysis of Multiple Traits Using "Optimal" Maximum Heritability Test.

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9.  Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits.

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Journal:  PLoS Genet       Date:  2018-10-05       Impact factor: 5.917

  9 in total

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