Pedigree disequilibrium tests for multilocus haplotypes

被引:1037
作者
Dudbridge, F [1 ]
机构
[1] MRC, Human Genome Mapping Project Resource Ctr, Cambridge CB10 1SB, England
关键词
TDT; PDT; association tests; family-based controls; haplotype analysis; EXTENDED TRANSMISSION/DISEQUILIBRIUM TEST; FAMILY-BASED TESTS; LINKAGE DISEQUILIBRIUM; ASSOCIATION; TRAITS; LIKELIHOOD; GENES; SNPS; TDT; HLA;
D O I
10.1002/gepi.10252
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Association tests of multilocus haplotypes are of interest both in linkage disequilibrium mapping and in candidate gene studies. For case-parent trios, I discuss the extension of existing multilocus methods to include ambiguous haplotypes in tests of models which distinguish between the cis and trans phase. A likelihood-ratio test is proposed, using the expectation-maximization (E-M) algorithm to account for haplotype ambiguities. Assumptions about the population structure are required, but realistic situations, including population stratification, which violate the assumptions lead to conservative tests. I describe a permutation procedure for the null hypothesis of interest, which controls for violation of the assumptions. For general pedigrees, I describe extensions of the pedigree disequilibrium test to include uncertain haplotypes. The summary statistics are replaced by their expected values over prior distributions of haplotype frequencies. If prior distributions are not available, a valid test is possible by using the E-M algorithm to estimate the null distribution of haplotype frequencies. Similar methods are available for quantitative traits. Exact permutation tests are difficult to construct in small samples, but an approximate procedure is appropriate in large samples, and can be used to account for dependencies between tests of multiple haplotypes and loci. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:115 / 121
页数:7
相关论文
共 29 条
[1]   A general test of association for quantitative traits in nuclear families [J].
Abecasis, GR ;
Cardon, LR ;
Cookson, WOC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :279-292
[2]   The relative power of SNPs and haplotype as genetic markers for association tests [J].
Bader, JS .
PHARMACOGENOMICS, 2001, 2 (01) :11-24
[3]  
Bitti PP, 2001, GENET EPIDEMIOL, V20, P271, DOI 10.1002/1098-2272(200102)20:2<271::AID-GEPI9>3.0.CO
[4]  
2-L
[5]  
BRESLOW NE, 1980, ANAL CASE CONTROL ST, V1
[6]   A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission [J].
Clayton, D .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) :1170-1177
[7]   A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data:: Application to HLA in type 1 diabetes [J].
Cordell, HJ ;
Clayton, DG .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :124-141
[8]  
CURTIS D, 1995, AM J HUM GENET, V56, P811
[9]   MAXIMUM LIKELIHOOD FROM INCOMPLETE DATA VIA EM ALGORITHM [J].
DEMPSTER, AP ;
LAIRD, NM ;
RUBIN, DB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-METHODOLOGICAL, 1977, 39 (01) :1-38
[10]  
Koeleman BPC, 2000, ANN HUM GENET, V64, P207, DOI 10.1017/S0003480000008095