Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence data

被引:3
作者
Yun Ju Sung
Treva K Rice
Dabeeru C Rao
机构
[1] Washington University School of Medicine,Division of Biostatistics
关键词
Minor Allele Frequency; Genetic Analysis Workshop; Proportion Test; Causal SNPs; Nonsynonymous SNPs;
D O I
10.1186/1753-6561-5-S9-S121
中图分类号
学科分类号
摘要
Genetic Analysis Workshop 17 used real sequence data from the 1000 Genomes Project and simulated phenotypes influenced by a large number of rare variants. Our aim is to evaluate the performance of various collapsing methods that were developed for analysis of multiple rare variants. We apply collapsing methods to continuous phenotypes Q1 and Q2 for all 200 replicates of the unrelated individuals data. Within each gene, we collapse (1) all SNPs, (2) all SNPs with minor allele frequency (MAF) < 0.05, and (3) nonsynonymous SNPs with MAF < 0.05. We consider two tests when collapsing variants: using the proportion of variants and using the presence/absence of any variant. We also compare our results to a single-marker analysis using PLINK. For phenotype Q1, the proportion test for collapsing rare nonsynonymous SNPs often performed the best. Two genes (FLT1 and KDR) had statistically significant results. A single-marker analysis using PLINK also provided statistically significant results for some SNPs within these two genes. For phenotype Q2, collapsing rare nonsynonymous SNPs performed the best, with almost no difference between proportion and presence tests. However, neither collapsing methods nor a single-marker analysis provided statistically significant results at the true genes for Q2. We also found that a large number of noncausal genes had high correlations with causal genes for Q1 and Q2, which may account for inflated false positives.
引用
收藏
相关论文
共 28 条
[1]  
Dering C(2011)Statistical analysis of rare sequence variants: an overview of collapsing methods Genet Epidemiol 3 12-17
[2]  
Pugh E(2010)An evaluation of statistical approaches to rare variant analysis in genetic association studies Genet Epidemiol 34 188-193
[3]  
Ziegler A(2011)Genetic Analysis Workshop 17 mini-exome simulation BMC Proc 5 S2-575
[4]  
Morris AP(2007)PLINK: A tool set for whole-genome association and population-based linkage analysis Am J Hum Genet 81 559-undefined
[5]  
Zeggini E(2011)Evaluating methods for the analysis of rare variants in sequence data BMC Proc 5 S119-undefined
[6]  
Almasy LA(undefined)undefined undefined undefined undefined-undefined
[7]  
Dyer TD(undefined)undefined undefined undefined undefined-undefined
[8]  
Peralta JM(undefined)undefined undefined undefined undefined-undefined
[9]  
Kent JW(undefined)undefined undefined undefined undefined-undefined
[10]  
Charlesworth JC(undefined)undefined undefined undefined undefined-undefined