Perspectives on genome-wide multi-stage family-based association studies

被引:3
作者
Van Steen, K. [1 ,2 ]
机构
[1] Univ Liege, Inst Montefiore, B-4000 Liege, Belgium
[2] Univ Liege, GIGA, Syst & Modelling Unit, B-4000 Liege, Belgium
关键词
genome-wide association; family-based association testing; multi-stage designs; QUANTITATIVE TRAIT LOCI; PARENTAL-GENOTYPE RECONSTRUCTION; PEDIGREE DISEQUILIBRIUM TEST; GENE-DISEASE ASSOCIATION; TRANSMISSION/DISEQUILIBRIUM TEST; COMPLEX DISEASES; LINKAGE DISEQUILIBRIUM; 2-STAGE DESIGNS; TRANSMISSION-DISEQUILIBRIUM; NUCLEAR FAMILIES;
D O I
10.1002/sim.4259
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the establishment of large consortiums of researchers, genome-wide association (GWA) studies have become increasingly popular and feasible. Although most of these association studies focus on unrelated individuals, a lot of advantages can be exploited by including families in the analysis as well. To overcome the additional genotyping cost, multi-stage designs are particularly useful. In this article, I offer a perspective view on genome-wide family-based association analyses, both within a model-based and model-free paradigm. I highlight how multi-stage designs and analysis techniques, which are quite popular in clinical epidemiology, can enter GWA settings. I furthermore discuss how they have proven successful in reducing analysis complexity, and in overcoming one of the most cumbersome statistical hurdles in the genome-wide context, namely controlling increased false positives due to multiple testing. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:2201 / 2221
页数:21
相关论文
共 173 条
[21]   FAM-MDR: A Flexible Family-Based Multifactor Dimensionality Reduction Technique to Detect Epistasis Using Related Individuals [J].
Cattaert, Tom ;
Urrea, Victor ;
Naj, Adam C. ;
De Lobel, Lizzy ;
De Wit, Vanessa ;
Fu, Mao ;
John, Jestinah M. Mahachie ;
Shen, Haiqing ;
Luz Calle, M. ;
Ritchie, Marylyn D. ;
Edwards, Todd L. ;
Van Steen, Kristel .
PLOS ONE, 2010, 5 (04)
[22]  
Chanda P, 2009, BMC P, V3, pS72
[23]   AMBIENCE: A Novel Approach and Efficient Algorithm for Identifying Informative Genetic and Environmental Associations With Complex Phenotypes [J].
Chanda, Pritam ;
Sucheston, Lara ;
Zhang, Aidong ;
Brazeau, Daniel ;
Freudenheim, Jo L. ;
Ambrosone, Christine ;
Ramanathan, Murali .
GENETICS, 2008, 180 (02) :1191-1210
[24]   Information-theoretic metrics for visualizing gene-environment interactions [J].
Chanda, Pritam ;
Zhang, Aidong ;
Brazeau, Daniel ;
Sucheston, Lara ;
Freudenheim, Jo L. ;
Ambrosone, Christine ;
Ramanathan, Murali .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (05) :939-963
[25]   Information-theoretic gene-gene and gene-environment interaction analysis of quantitative traits [J].
Chanda, Pritam ;
Sucheston, Lara ;
Liu, Song ;
Zhang, Aidong ;
Ramanathan, Murali .
BMC GENOMICS, 2009, 10 :509
[26]   The interaction index, a novel information-theoretic metric for prioritizing interacting genetic variations and environmental factors [J].
Chanda, Pritam ;
Sucheston, Lara ;
Zhang, Aidong ;
Ramanathan, Murali .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (10) :1274-1286
[27]   Family-based association tests for genomewide association scans [J].
Chen, Wei-Min ;
Abecasis, Goncalo R. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (05) :913-926
[28]   Conjuring SNPs to detect associations [J].
Clark, Andrew G. ;
Li, Jian .
NATURE GENETICS, 2007, 39 (07) :815-816
[29]   Transmission/disequilibrium tests for extended marker haplotypes [J].
Clayton, D ;
Jones, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) :1161-1169
[30]  
Cleves MA, 1997, GENET EPIDEMIOL, V14, P337, DOI 10.1002/(SICI)1098-2272(1997)14:4<337::AID-GEPI1>3.3.CO