An Overview of the Genetic Dissection of Complex Traits

被引:25
|
作者
Rao, D. C. [1 ,2 ,3 ,4 ]
机构
[1] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Math, St Louis, MO 63110 USA
关键词
D O I
10.1016/S0065-2660(07)00401-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Thanks to the recent revolutionary genomic advances such as the International HapMap consortium, resolution of the genetic architecture of common complex traits is beginning to look hopeful. While demonstrating the feasibility of genome-wide association (GWA) studies, the pathbreaking Wellcome Trust Case Control Consortium (WTCCC) study also serves to underscore the critical importance of very large sample sizes and draws attention to potential problems, which need to be addressed as part of the study design. Even the large WTCCC study had vastly inadequate power for several of the associations reported (and confirmed) and, therefore, most of the regions harboring relevant associations may not be identified anytime soon. This chapter provides an overview of some of the key developments in the methodological approaches to genetic dissection of common complex traits. Constrained Bayesian networks are suggested as especially useful for analysis of pathway-based SNPs. Likewise, composite likelihood is suggested as a promising method for modeling complex systems. It discusses the key steps in a study design, with an emphasis on GWA studies. Potential limitations highlighted by the WTCCC GWA study are discussed, including problems associated with massive genotype imputation, analysis of pooled national samples, shared controls, and the critical role of interactions. GWA studies clearly need massive sample sizes that are only possible through genuine collaborations. After all, for common complex traits, the question is not whether we can find some pieces of the puzzle, but how large and what kind of a sample we need to (nearly) solve the genetic puzzle. (C) 2008, Elsevier Inc.
引用
收藏
页码:3 / 34
页数:32
相关论文
共 50 条
  • [21] Genetic dissection of complex traits In silico:: Approaches, problems and solutions
    Zhao, Jing Hua
    Tan, Qihua
    CURRENT BIOINFORMATICS, 2006, 1 (03) : 359 - 369
  • [22] Experimental strategies for the genetic dissection of complex traits in animal models
    Ariel Darvasi
    Nature Genetics, 1998, 18 : 19 - 24
  • [23] Genetic Dissection of Diabetes in a Mouse Model of Human Complex Traits
    Ikegami, Hiroshi
    CLINICAL AND EXPERIMENTAL HYPERTENSION, 2011, 33 (01) : 1 - 1
  • [24] Genetic dissection of complex behaviour traits in German Shepherd dogs
    Juliane Friedrich
    Erling Strandberg
    Per Arvelius
    E. Sánchez-Molano
    Ricardo Pong-Wong
    John M. Hickey
    Marie J. Haskell
    Pamela Wiener
    Heredity, 2019, 123 : 746 - 758
  • [25] Quantitative genetic dissection of complex traits in a QTL-mapping pedigree
    Wu, RL
    THEORETICAL AND APPLIED GENETICS, 1996, 93 (03) : 447 - 457
  • [26] GENETIC DISSECTION OF COMPLEX TRAITS - GUIDELINES FOR INTERPRETING AND REPORTING LINKAGE RESULTS
    LANDER, E
    KRUGLYAK, L
    NATURE GENETICS, 1995, 11 (03) : 241 - 247
  • [28] GENETIC DISSECTION OF COMPLEX TRAITS (VOL 265, PG 2037, 1994)
    LANDER, ES
    SCHORK, NJ
    SCIENCE, 1994, 266 (5184) : 353 - 353
  • [29] A new approach to the problem of multiple comparisons in the genetic dissection of complex traits
    Weller, JI
    Song, JZ
    Heyen, DW
    Lewin, HA
    Ron, M
    GENETICS, 1998, 150 (04) : 1699 - 1706
  • [30] Rat models of autoimmune diseases: The genetic dissection of complex traits.
    Salstrom, J
    Furuya, T
    Cannon, GW
    Remmers, EF
    Griffiths, MM
    Wilder, RL
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A467 - A467