Generalized genomic distance-based regression methodology for multilocus association analysis

被引:131
作者
Wessel, Jennifer
Schork, Nicholas J.
机构
[1] Univ Calif San Diego, Dept Psychiat, Polymorphism Res Lab, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Div Epidemiol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Div Biostat, Dept Family & Prevent Med, Moores Canc Ctr, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Ctr Human Genet & Genom, Calif Inst Telecommun & Informat Technol, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, San Diego Supercomp Ctr, La Jolla, CA 92093 USA
[6] San Diego State Univ, Grad Program Publ Hlth, San Diego, CA 92182 USA
关键词
D O I
10.1086/508346
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Large-scale, multilocus genetic association studies require powerful and appropriate statistical-analysis tools that are designed to relate genotype and haplotype information to phenotypes of interest. Many analysis approaches consider relating allelic, haplotypic, or genotypic information to a trait through use of extensions of traditional analysis techniques, such as contingency-table analysis, regression methods, and analysis-of-variance techniques. In this work, we consider a complementary approach that involves the characterization and measurement of the similarity and dissimilarity of the allelic composition of a set of individuals' diploid genomes at multiple loci in the regions of interest. We describe a regression method that can be used to relate variation in the measure of genomic dissimilarity (or "distance") among a set of individuals to variation in their trait values. Weighting factors associated with functional or evolutionary conservation information of the loci can be used in the assessment of similarity. The proposed method is very flexible and is easily extended to complex multilocus-analysis settings involving covariates. In addition, the proposed method actually encompasses both single-locus and haplotype-phylogeny analysis methods, which are two of the most widely used approaches in genetic association analysis. We showcase the method with data described in the literature. Ultimately, our method is appropriate for high-dimensional genomic data and anticipates an era when cost-effective exhaustive DNA sequence data can be obtained for a large number of individuals, over and above genotype information focused on a few well-chosen loci.
引用
收藏
页码:792 / 806
页数:15
相关论文
共 55 条
[1]   A haplotype map of the human genome [J].
Altshuler, D ;
Brooks, LD ;
Chakravarti, A ;
Collins, FS ;
Daly, MJ ;
Donnelly, P ;
Gibbs, RA ;
Belmont, JW ;
Boudreau, A ;
Leal, SM ;
Hardenbol, P ;
Pasternak, S ;
Wheeler, DA ;
Willis, TD ;
Yu, FL ;
Yang, HM ;
Zeng, CQ ;
Gao, Y ;
Hu, HR ;
Hu, WT ;
Li, CH ;
Lin, W ;
Liu, SQ ;
Pan, H ;
Tang, XL ;
Wang, J ;
Wang, W ;
Yu, J ;
Zhang, B ;
Zhang, QR ;
Zhao, HB ;
Zhao, H ;
Zhou, J ;
Gabriel, SB ;
Barry, R ;
Blumenstiel, B ;
Camargo, A ;
Defelice, M ;
Faggart, M ;
Goyette, M ;
Gupta, S ;
Moore, J ;
Nguyen, H ;
Onofrio, RC ;
Parkin, M ;
Roy, J ;
Stahl, E ;
Winchester, E ;
Ziaugra, L ;
Shen, Y .
NATURE, 2005, 437 (7063) :1299-1320
[2]   A new method for non-parametric multivariate analysis of variance [J].
Anderson, MJ .
AUSTRAL ECOLOGY, 2001, 26 (01) :32-46
[3]  
[Anonymous], 1995, Randomization tests
[4]   Clustering of haplotypes based on phylogeny:: how good a strategy for association testing? [J].
Bardel, C ;
Darlu, P ;
Génin, E .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (02) :202-206
[5]   IDENTIX, a software to test for relatedness in a population using permutation methods [J].
Belkhir, K ;
Castric, V ;
Bonhomme, F .
MOLECULAR ECOLOGY NOTES, 2002, 2 (04) :611-614
[6]   Automated whole-genome multiple alignment of rat, mouse, and human [J].
Brudno, M ;
Poliakov, A ;
Salamov, A ;
Cooper, GM ;
Sidow, A ;
Rubin, EM ;
Solovyev, V ;
Batzoglou, S ;
Dubchak, I .
GENOME RESEARCH, 2004, 14 (04) :685-692
[7]   Mapping determinants of human gene expression by regional and genome-wide association [J].
Cheung, VG ;
Spielman, RS ;
Ewens, KG ;
Weber, TM ;
Morley, M ;
Burdick, JT .
NATURE, 2005, 437 (7063) :1365-1369
[8]   Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase [J].
Clark, AG ;
Weiss, KM ;
Nickerson, DA ;
Taylor, SL ;
Buchanan, A ;
Stengård, J ;
Salomaa, V ;
Vartiainen, E ;
Perola, M ;
Boerwinkle, E ;
Sing, CF .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :595-612
[9]   Complex promoter and coding region β2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness [J].
Drysdale, CM ;
McGraw, DW ;
Stack, CB ;
Stephens, JC ;
Judson, RS ;
Nandabalan, K ;
Arnold, K ;
Ruano, G ;
Liggett, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10483-10488
[10]  
EXCOFFIER L, 1992, GENETICS, V131, P479