The optimal measure of allelic association

被引:87
作者
Morton, NE
Zhang, W
Taillon-Miller, P
Ennis, S
Kwok, PY
Collins, A
机构
[1] Southampton Gen Hosp, Human Genet Res Div, Southampton SO16 6YD, Hants, England
[2] Washington Univ, Sch Med, Div Dermatol, St Louis, MO 63110 USA
关键词
D O I
10.1073/pnas.091062198
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Allelic association between pairs of loci is derived in terms of the association probability rho as a function of recombination theta, effective population size N, linear systematic pressure v, and time t, predicting both rho (rt), the decrease of association from founders and rho (ct), the increase by genetic drift, with rho (t) = rho (rt) + rho (ct). These results conform to the Malecot equation, with time replaced by distance on the genetic map, or on the physical map if recombination in the region is uniform. Earlier evidence suggested that rho is less sensitive to variations in marker allele frequencies than alternative metrics for which there is no probability theory. This robustness is confirmed for six alternatives in eight samples. In none of these 48 tests was the residual variance as small as for rho. Overall, efficiency was less than 80% for all alternatives, and less than 30% for two of them, Efficiency of alternatives did not increase when information was estimated simultaneously. The swept radius within which substantial values of rho are conserved lies between 385 and 893 kb, but deviation of parameters between measures is enormously significant. The large effort now being devoted to allelic association has little value unless the rho metric with the strongest theoretical basis and least sensitivity to marker allele frequencies is used for mapping of marker association and localization of disease loci.
引用
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页码:5217 / 5221
页数:5
相关论文
共 33 条
[1]  
[Anonymous], 1990, GENETIC DATA ANAL
[2]  
Arunachalam V, 1971, POLYMORPHISMS LINKED
[3]   Mapping a disease locus by allelic association [J].
Collins, A ;
Morton, NE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1741-1745
[4]   Genetic epidemiology of single-nucleotide polymorphisms [J].
Collins, A ;
Lonjou, C ;
Morton, NE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15173-15177
[5]  
COLLINS A, 2001, IN PRESS HUM MUTAT
[6]  
Cordell HJ, 1999, GENET EPIDEMIOL, V17, P237, DOI 10.1002/(SICI)1098-2272(199911)17:4<237::AID-GEPI1>3.0.CO
[7]  
2-P
[8]   The variant call format and VCFtools [J].
Danecek, Petr ;
Auton, Adam ;
Abecasis, Goncalo ;
Albers, Cornelis A. ;
Banks, Eric ;
DePristo, Mark A. ;
Handsaker, Robert E. ;
Lunter, Gerton ;
Marth, Gabor T. ;
Sherry, Stephen T. ;
McVean, Gilean ;
Durbin, Richard .
BIOINFORMATICS, 2011, 27 (15) :2156-2158
[9]   A COMPARISON OF LINKAGE DISEQUILIBRIUM MEASURES FOR FINE-SCALE MAPPING [J].
DEVLIN, B ;
RISCH, N .
GENOMICS, 1995, 29 (02) :311-322
[10]  
Eaves IA, 2000, NAT GENET, V25, P320