Model choice in gene mapping:: what and why

被引:84
作者
Sillanpää, MJ [1 ]
Corander, J [1 ]
机构
[1] Univ Helsinki, Rolf Nevanlinna Inst, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
D O I
10.1016/S0168-9525(02)02688-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The choice of an appropriate genetic model describing the genetic architecture underlying a character of interest is an inherent part of the gene mapping studies of human and other living organisms. The genetic model specifies the statistical parameters for the number of genes, their positions, and the types and magnitudes of their contributions to the phenotype. There are many considerations involved in model formulation (choice) ranging from the assumptions concerning the data, the role of environment, and the number of oligogenes (or quantitative trait loci) influencing the trait behavior. There are several model selection procedures and criteria under specific sampling designs in the genetic literature. These approaches often have their origin in computer science or in general statistical theory. Our aim here is to give an overview of the most popular statistical criteria and to present principles behind them. Bayesian model averaging is suggested as a robust alternative for such methods.
引用
收藏
页码:301 / 307
页数:7
相关论文
共 55 条
[1]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[2]   Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[3]  
[Anonymous], 1996, PARAMETRIC STAT INFE
[4]  
[Anonymous], 1986, NUMERICAL RECIPES C
[5]  
Ball RD, 2001, GENETICS, V159, P1351
[6]  
BROMAN KW, 1999, STAT GENETICS MOL BI, P114
[7]  
BROMAN KW, IN PRESS J R STAT B
[8]  
Carlborg Ö, 2000, GENETICS, V155, P2003
[9]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[10]  
Cockerham CC, 1996, GENETICS, V143, P1437