Promise and pitfalls of the Immunochip

被引:373
作者
Cortes, Adrian [1 ]
Brown, Matthew A. [1 ]
机构
[1] Univ Queensland, Diamantina Inst, Princess Alexandra Hosp, Brisbane, Qld 4102, Australia
关键词
MISSING HERITABILITY; HUMAN HEIGHT; DISEASES;
D O I
10.1186/ar3204
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genomewide association studies (GWAS) have proven a powerful hypothesis-free method to identify common disease-associated variants. Even quite large GWAS, however, have only at best identified moderate proportions of the genetic variants contributing to disease heritability. To provide cost-effective genotyping of common and rare variants to map the remaining heritability and to fine-map established loci, the Immunochip Consortium has developed a 200,000 SNP chip that has been produced in very large numbers for a fraction of the cost of GWAS chips. This chip provides a powerful tool for immunogenetics gene mapping.
引用
收藏
页数:3
相关论文
共 8 条
  • [1] Hundreds of variants clustered in genomic loci and biological pathways affect human height
    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
    [J]. NATURE, 2010, 467 (7317) : 832 - 838
  • [2] Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
    Craddock, Nick
    Hurles, Matthew E.
    Cardin, Niall
    Pearson, Richard D.
    Plagnol, Vincent
    Robson, Samuel
    Vukcevic, Damjan
    Barnes, Chris
    Conrad, Donald F.
    Giannoulatou, Eleni
    Holmes, Chris
    Marchini, Jonathan L.
    Stirrups, Kathy
    Tobin, Martin D.
    Wain, Louise V.
    Yau, Chris
    Aerts, Jan
    Ahmad, Tariq
    Andrews, T. Daniel
    Arbury, Hazel
    Attwood, Anthony
    Auton, Adam
    Ball, Stephen G.
    Balmforth, Anthony J.
    Barrett, Jeffrey C.
    Barroso, Ines
    Barton, Anne
    Bennett, Amanda J.
    Bhaskar, Sanjeev
    Blaszczyk, Katarzyna
    Bowes, John
    Brand, Oliver J.
    Braund, Peter S.
    Bredin, Francesca
    Breen, Gerome
    Brown, Morris J.
    Bruce, Ian N.
    Bull, Jaswinder
    Burren, Oliver S.
    Burton, John
    Byrnes, Jake
    Caesar, Sian
    Clee, Chris M.
    Coffey, Alison J.
    Connell, John M. C.
    Cooper, Jason D.
    Dominiczak, Anna F.
    Downes, Kate
    Drummond, Hazel E.
    Dudakia, Darshna
    [J]. NATURE, 2010, 464 (7289) : 713 - U86
  • [3] DNA methylation profiles in monozygotic and dizygotic twins
    Kaminsky, Zachary A.
    Tang, Thomas
    Wang, Sun-Chong
    Ptak, Carolyn
    Oh, Gabriel H. T.
    Wong, Albert H. C.
    Feldcamp, Laura A.
    Virtanen, Carl
    Halfvarson, Jonas
    Tysk, Curt
    McRae, Allan F.
    Visscher, Peter M.
    Montgomery, Grant W.
    Gottesman, Irving I.
    Martin, Nicholas G.
    Petronis, Art
    [J]. NATURE GENETICS, 2009, 41 (02) : 240 - 245
  • [4] Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies
    Keating, Brendan J.
    Tischfield, Sam
    Murray, Sarah S.
    Bhangale, Tushar
    Price, Thomas S.
    Glessner, Joseph T.
    Galver, Luana
    Barrett, Jeffrey C.
    Grant, Struan F. A.
    Farlow, Deborah N.
    Chandrupatla, Hareesh R.
    Hansen, Mark
    Ajmal, Saad
    Papanicolaou, George J.
    Guo, Yiran
    Li, Mingyao
    DerOhannessian, Stephanie
    de Bakker, Paul I. W.
    Bailey, Swneke D.
    Montpetit, Alexandre
    Edmondson, Andrew C.
    Taylor, Kent
    Gai, Xiaowu
    Wang, Susanna S.
    Fornage, Myriam
    Shaikh, Tamim
    Groop, Leif
    Boehnke, Michael
    Hall, Alistair S.
    Hattersley, Andrew T.
    Frackelton, Edward
    Patterson, Nick
    Chiang, Charleston W. K.
    Kim, Cecelia E.
    Fabsitz, Richard R.
    Ouwehand, Willem
    Price, Alkes L.
    Munroe, Patricia
    Caulfield, Mark
    Drake, Thomas
    Boerwinkle, Eric
    Reich, David
    Whitehead, A. Stephen
    Cappola, Thomas P.
    Samani, Nilesh J.
    Lusis, A. Jake
    Schadt, Eric
    Wilson, James G.
    Koenig, Wolfgang
    McCarthy, Mark I.
    [J]. PLOS ONE, 2008, 3 (10):
  • [5] A statistical method for predicting classical HLA alleles from SNP data
    Leslie, Stephen
    Donnelly, Peter
    McVean, Gil
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) : 48 - 56
  • [6] Finding the missing heritability of complex diseases
    Manolio, Teri A.
    Collins, Francis S.
    Cox, Nancy J.
    Goldstein, David B.
    Hindorff, Lucia A.
    Hunter, David J.
    McCarthy, Mark I.
    Ramos, Erin M.
    Cardon, Lon R.
    Chakravarti, Aravinda
    Cho, Judy H.
    Guttmacher, Alan E.
    Kong, Augustine
    Kruglyak, Leonid
    Mardis, Elaine
    Rotimi, Charles N.
    Slatkin, Montgomery
    Valle, David
    Whittemore, Alice S.
    Boehnke, Michael
    Clark, Andrew G.
    Eichler, Evan E.
    Gibson, Greg
    Haines, Jonathan L.
    Mackay, Trudy F. C.
    McCarroll, Steven A.
    Visscher, Peter M.
    [J]. NATURE, 2009, 461 (7265) : 747 - 753
  • [7] Epigenetic Inheritance and the Missing Heritability Problem
    Slatkin, Montgomery
    [J]. GENETICS, 2009, 182 (03) : 845 - 850
  • [8] Common SNPs explain a large proportion of the heritability for human height
    Yang, Jian
    Benyamin, Beben
    McEvoy, Brian P.
    Gordon, Scott
    Henders, Anjali K.
    Nyholt, Dale R.
    Madden, Pamela A.
    Heath, Andrew C.
    Martin, Nicholas G.
    Montgomery, Grant W.
    Goddard, Michael E.
    Visscher, Peter M.
    [J]. NATURE GENETICS, 2010, 42 (07) : 565 - U131