Literature DB >> 26707090

Regionally Smoothed Meta-Analysis Methods for GWAS Datasets.

Ferdouse Begum1, Monir H Sharker2, Stephanie L Sherman3, George C Tseng4,5, Eleanor Feingold4,5.   

Abstract

Genome-wide association studies are proven tools for finding disease genes, but it is often necessary to combine many cohorts into a meta-analysis to detect statistically significant genetic effects. Often the component studies are performed by different investigators on different populations, using different chips with minimal SNPs overlap. In some cases, raw data are not available for imputation so that only the genotyped single nucleotide polymorphisms (SNPs) results can be used in meta-analysis. Even when SNP sets are comparable, different cohorts may have peak association signals at different SNPs within the same gene due to population differences in linkage disequilibrium or environmental interactions. We hypothesize that the power to detect statistical signals in these situations will improve by using a method that simultaneously meta-analyzes and smooths the signal over nearby markers. In this study, we propose regionally smoothed meta-analysis methods and compare their performance on real and simulated data.
© 2015 WILEY PERIODICALS, INC.

Entities:  

Keywords:  GWAS meta-analysis; simulation; sliding-window; window-based method

Mesh:

Year:  2015        PMID: 26707090      PMCID: PMC4724289          DOI: 10.1002/gepi.21949

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  25 in total

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Authors:  M Kanehisa; S Goto
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3.  Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects.

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Journal:  Neuroimage       Date:  2011-04-08       Impact factor: 6.556

4.  Detecting haplotype effects in genomewide association studies.

Authors:  B E Huang; C I Amos; D Y Lin
Journal:  Genet Epidemiol       Date:  2007-12       Impact factor: 2.135

5.  ATOM: a powerful gene-based association test by combining optimally weighted markers.

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6.  Probability that a two-stage genome-wide association study will detect a disease-associated snp and implications for multistage designs.

Authors:  M H Gail; R M Pfeiffer; W Wheeler; D Pee
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7.  HapBoost: a fast approach to boosting haplotype association analyses in genome-wide association studies.

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Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2013 Jan-Feb       Impact factor: 3.710

Review 8.  Comprehensive literature review and statistical considerations for GWAS meta-analysis.

Authors:  Ferdouse Begum; Debashis Ghosh; George C Tseng; Eleanor Feingold
Journal:  Nucleic Acids Res       Date:  2012-01-12       Impact factor: 16.971

9.  Genetic analysis of variation in human meiotic recombination.

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10.  Fast and accurate haplotype frequency estimation for large haplotype vectors from pooled DNA data.

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Journal:  Eur J Med Res       Date:  2017-12-28       Impact factor: 2.175

2.  A Multiple-Trait Bayesian Variable Selection Regression Method for Integrating Phenotypic Causal Networks in Genome-Wide Association Studies.

Authors:  Zigui Wang; Deborah Chapman; Gota Morota; Hao Cheng
Journal:  G3 (Bethesda)       Date:  2020-12-03       Impact factor: 3.154

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