Literature DB >> 21217123

Robust linear regression methods in association studies.

V M Lourenço1, A M Pires, M Kirst.   

Abstract

MOTIVATION: It is well known that data deficiencies, such as coding/rounding errors, outliers or missing values, may lead to misleading results for many statistical methods. Robust statistical methods are designed to accommodate certain types of those deficiencies, allowing for reliable results under various conditions. We analyze the case of statistical tests to detect associations between genomic individual variations (SNP) and quantitative traits when deviations from the normality assumption are observed. We consider the classical analysis of variance tests for the parameters of the appropriate linear model and a robust version of those tests based on M-regression. We then compare their empirical power and level using simulated data with several degrees of contamination.
RESULTS: Data normality is nothing but a mathematical convenience. In practice, experiments usually yield data with non-conforming observations. In the presence of this type of data, classical least squares statistical methods perform poorly, giving biased estimates, raising the number of spurious associations and often failing to detect true ones. We show through a simulation study and a real data example, that the robust methodology can be more powerful and thus more adequate for association studies than the classical approach. AVAILABILITY: The code of the robustified version of function lmekin() from the R package kinship is provided as Supplementary Material.

Mesh:

Year:  2011        PMID: 21217123     DOI: 10.1093/bioinformatics/btr006

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  11 in total

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2.  Satiety does not alter the ventral striatum's response to immediate reward in bulimia nervosa.

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3.  A robust Bayesian genome-based median regression model.

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4.  Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy.

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5.  Genomics of post-prandial lipidomic phenotypes in the Genetics of Lipid lowering Drugs and Diet Network (GOLDN) study.

Authors:  Marguerite R Irvin; Degui Zhi; Stella Aslibekyan; Steven A Claas; Devin M Absher; Jose M Ordovas; Hemant K Tiwari; Steve Watkins; Donna K Arnett
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Journal:  PLoS Genet       Date:  2014-10-23       Impact factor: 5.917

7.  Genomics of Postprandial Lipidomics in the Genetics of Lipid-Lowering Drugs and Diet Network Study.

Authors:  Marguerite R Irvin; May E Montasser; Tobias Kind; Sili Fan; Dinesh K Barupal; Amit Patki; Rikki M Tanner; Nicole D Armstrong; Kathleen A Ryan; Steven A Claas; Jeffrey R O'Connell; Hemant K Tiwari; Donna K Arnett
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8.  Genome-wide epistatic expression quantitative trait loci discovery in four human tissues reveals the importance of local chromosomal interactions governing gene expression.

Authors:  Darren J Fitzpatrick; Colm J Ryan; Naisha Shah; Derek Greene; Cliona Molony; Denis C Shields
Journal:  BMC Genomics       Date:  2015-02-21       Impact factor: 3.969

9.  Epigenome-wide association study of metabolic syndrome in African-American adults.

Authors:  Tomi Akinyemiju; Anh N Do; Amit Patki; Stella Aslibekyan; Degui Zhi; Bertha Hidalgo; Hemant K Tiwari; Devin Absher; Xin Geng; Donna K Arnett; Marguerite R Irvin
Journal:  Clin Epigenetics       Date:  2018-04-10       Impact factor: 6.551

10.  Metabolic and inflammatory biomarkers are associated with epigenetic aging acceleration estimates in the GOLDN study.

Authors:  Marguerite R Irvin; Stella Aslibekyan; Anh Do; Degui Zhi; Bertha Hidalgo; Steven A Claas; Vinodh Srinivasasainagendra; Steve Horvath; Hemant K Tiwari; Devin M Absher; Donna K Arnett
Journal:  Clin Epigenetics       Date:  2018-04-18       Impact factor: 6.551

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