Analysing biological pathways in genome-wide association studies

被引:601
作者
Wang, Kai [1 ,2 ]
Li, Mingyao [3 ]
Hakonarson, Hakon [1 ,4 ]
机构
[1] Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA
[2] Univ So Calif, Dept Psychol, Zilkha Neurogenet Inst, Dept Prevent Med, Los Angeles, CA 90089 USA
[3] Univ Penn, Dept Biostat & Epidemiol, Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Pediat, Sch Med, Philadelphia, PA 19104 USA
关键词
SET ENRICHMENT ANALYSIS; FACTOR-H POLYMORPHISM; GENE-EXPRESSION DATA; SUSCEPTIBILITY LOCI; COMMON DISEASES; MULTIPLE LOCI; VARIANTS; CYTOSCAPE; INSIGHTS; SNP;
D O I
10.1038/nrg2884
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide association (GWA) studies have typically focused on the analysis of single markers, which often lacks the power to uncover the relatively small effect sizes conferred by most genetic variants. Recently, pathway-based approaches have been developed, which use prior biological knowledge on gene function to facilitate more powerful analysis of GWA study data sets. These approaches typically examine whether a group of related genes in the same functional pathway are jointly associated with a trait of interest. Here we review the development of pathway-based approaches for GWA studies, discuss their practical use and caveats, and suggest that pathway-based approaches may also be useful for future GWA studies with sequencing data.
引用
收藏
页码:843 / 854
页数:12
相关论文
共 113 条
[1]   InterIeukin-23/Th17 Pathways and Inflammatory Bowel Disease [J].
Abraham, Clara ;
Cho, Judy .
INFLAMMATORY BOWEL DISEASES, 2009, 15 (07) :1090-1100
[2]   IL-23 and Autoimmunity: New Insights into the Pathogenesis of Inflammatory Bowel Disease [J].
Abraham, Clara ;
Cho, Judy H. .
ANNUAL REVIEW OF MEDICINE, 2009, 60 :97-110
[3]   A general modular framework for gene set enrichment analysis [J].
Ackermann, Marit ;
Strimmer, Korbinian .
BMC BIOINFORMATICS, 2009, 10
[4]   Hundreds of variants clustered in genomic loci and biological pathways affect human height [J].
Allen, Hana Lango ;
Estrada, Karol ;
Lettre, Guillaume ;
Berndt, Sonja I. ;
Weedon, Michael N. ;
Rivadeneira, Fernando ;
Willer, Cristen J. ;
Jackson, Anne U. ;
Vedantam, Sailaja ;
Raychaudhuri, Soumya ;
Ferreira, Teresa ;
Wood, Andrew R. ;
Weyant, Robert J. ;
Segre, Ayellet V. ;
Speliotes, Elizabeth K. ;
Wheeler, Eleanor ;
Soranzo, Nicole ;
Park, Ju-Hyun ;
Yang, Jian ;
Gudbjartsson, Daniel ;
Heard-Costa, Nancy L. ;
Randall, Joshua C. ;
Qi, Lu ;
Smith, Albert Vernon ;
Maegi, Reedik ;
Pastinen, Tomi ;
Liang, Liming ;
Heid, Iris M. ;
Luan, Jian'an ;
Thorleifsson, Gudmar ;
Winkler, Thomas W. ;
Goddard, Michael E. ;
Lo, Ken Sin ;
Palmer, Cameron ;
Workalemahu, Tsegaselassie ;
Aulchenko, Yurii S. ;
Johansson, Asa ;
Zillikens, M. Carola ;
Feitosa, Mary F. ;
Esko, Tonu ;
Johnson, Toby ;
Ketkar, Shamika ;
Kraft, Peter ;
Mangino, Massimo ;
Prokopenko, Inga ;
Absher, Devin ;
Albrecht, Eva ;
Ernst, Florian ;
Glazer, Nicole L. ;
Hayward, Caroline .
NATURE, 2010, 467 (7317) :832-838
[5]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[6]   Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission [J].
Askland, Kathleen ;
Read, Cynthia ;
Moore, Jason .
HUMAN GENETICS, 2009, 125 (01) :63-79
[7]   Pathway analysis comparison using Crohn's disease genome wide association studies [J].
Ballard, David ;
Abraham, Clara ;
Cho, Judy ;
Zhao, Hongyu .
BMC MEDICAL GENOMICS, 2010, 3
[8]  
BALLARD DH, 2009, BMC P S7, V3, P91
[9]   Pathway and network-based analysis of genome-wide association studies in multiple sclerosis [J].
Baranzini, Sergio E. ;
Galwey, Nicholas W. ;
Wang, Joanne ;
Khankhanian, Pouya ;
Lindberg, Raija ;
Pelletier, Daniel ;
Wu, Wen ;
Uitdehaag, Bernard M. J. ;
Kappos, Ludwig ;
Polman, Chris H. ;
Matthews, Paul M. ;
Hauser, Stephen L. ;
Gibson, Rachel A. ;
Oksenberg, Jorge R. ;
Barnes, Michael R. .
HUMAN MOLECULAR GENETICS, 2009, 18 (11) :2078-2090
[10]   Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease [J].
Barrett, Jeffrey C. ;
Hansoul, Sarah ;
Nicolae, Dan L. ;
Cho, Judy H. ;
Duerr, Richard H. ;
Rioux, John D. ;
Brant, Steven R. ;
Silverberg, Mark S. ;
Taylor, Kent D. ;
Barmada, M. Michael ;
Bitton, Alain ;
Dassopoulos, Themistocles ;
Datta, Lisa Wu ;
Green, Todd ;
Griffiths, Anne M. ;
Kistner, Emily O. ;
Murtha, Michael T. ;
Regueiro, Miguel D. ;
Rotter, Jerome I. ;
Schumm, L. Philip ;
Steinhart, A. Hillary ;
Targan, Stephan R. ;
Xavier, Ramnik J. ;
Libioulle, Cecile ;
Sandor, Cynthia ;
Lathrop, Mark ;
Belaiche, Jacques ;
Dewit, Olivier ;
Gut, Ivo ;
Heath, Simon ;
Laukens, Debby ;
Mni, Myriam ;
Rutgeerts, Paul ;
Van Gossum, Andre ;
Zelenika, Diana ;
Franchimont, Denis ;
Hugot, Jean-Pierre ;
de Vos, Martine ;
Vermeire, Severine ;
Louis, Edouard ;
Cardon, Lon R. ;
Anderson, Carl A. ;
Drummond, Hazel ;
Nimmo, Elaine ;
Ahmad, Tariq ;
Prescott, Natalie J. ;
Onnie, Clive M. ;
Fisher, Sheila A. ;
Marchini, Jonathan ;
Ghori, Jilur .
NATURE GENETICS, 2008, 40 (08) :955-962