LocusZoom: regional visualization of genome-wide association scan results

被引:2026
作者
Pruim, Randall J. [3 ]
Welch, Ryan P. [1 ,2 ,4 ]
Sanna, Serena [5 ]
Teslovich, Tanya M. [1 ,2 ]
Chines, Peter S. [6 ]
Gliedt, Terry P. [1 ,2 ]
Boehnke, Michael [1 ,2 ]
Abecasis, Goncalo R. [1 ,2 ]
Willer, Cristen J. [1 ,2 ]
机构
[1] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Ctr Stat Genet, Ann Arbor, MI 48109 USA
[3] Calvin Coll, Dept Math & Stat, Grand Rapids, MI 49546 USA
[4] Univ Michigan, Sch Med, Bioinformat Grad Program, Ann Arbor, MI 48109 USA
[5] Cittadella Univ Monserrato, CNR, INN, I-09042 Cagliari, Italy
[6] NHGRI, NIH, Bethesda, MD 20892 USA
关键词
COMMON VARIANTS; IDENTIFICATION; SNPS; TOOL;
D O I
10.1093/bioinformatics/btq419
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genome-wide association studies (GWAS) have revealed hundreds of loci associated with common human genetic diseases and traits. We have developed a web-based plotting tool that provides fast visual display of GWAS results in a publication-ready format. LocusZoom visually displays regional information such as the strength and extent of the association signal relative to genomic position, local linkage disequilibrium (LD) and recombination patterns and the positions of genes in the region.
引用
收藏
页码:2336 / 2337
页数:2
相关论文
共 8 条
[1]   Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus [J].
Bush, William S. ;
Dudek, Scott M. ;
Ritchie, Marylyn D. .
BIOINFORMATICS, 2010, 26 (04) :578-579
[2]   SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap [J].
Johnson, Andrew D. ;
Handsaker, Robert E. ;
Pulit, Sara L. ;
Nizzari, Marcia M. ;
O'Donnell, Christopher J. ;
de Bakker, Paul I. W. .
BIOINFORMATICS, 2008, 24 (24) :2938-2939
[3]   VALID: Visualization of Association Study Results and Linkage Disequilibrium [J].
Jorgenson, Eric ;
Kvale, Mark ;
Witte, John S. .
GENETIC EPIDEMIOLOGY, 2009, 33 (07) :599-603
[4]   Common variants at 30 loci contribute to polygenic dyslipidemia [J].
Kathiresan, Sekar ;
Willer, Cristen J. ;
Peloso, Gina M. ;
Demissie, Serkalem ;
Musunuru, Kiran ;
Schadt, Eric E. ;
Kaplan, Lee ;
Bennett, Derrick ;
Li, Yun ;
Tanaka, Toshiko ;
Voight, Benjamin F. ;
Bonnycastle, Lori L. ;
Jackson, Anne U. ;
Crawford, Gabriel ;
Surti, Aarti ;
Guiducci, Candace ;
Burtt, Noel P. ;
Parish, Sarah ;
Clarke, Robert ;
Zelenika, Diana ;
Kubalanza, Kari A. ;
Morken, Mario A. ;
Scott, Laura J. ;
Stringham, Heather M. ;
Galan, Pilar ;
Swift, Amy J. ;
Kuusisto, Johanna ;
Bergman, Richard N. ;
Sundvall, Jouko ;
Laakso, Markku ;
Ferrucci, Luigi ;
Scheet, Paul ;
Sanna, Serena ;
Uda, Manuela ;
Yang, Qiong ;
Lunetta, Kathryn L. ;
Dupuis, Josee ;
de Bakker, Paul I. W. ;
O'Donnell, Christopher J. ;
Chambers, John C. ;
Kooner, Jaspal S. ;
Hercberg, Serge ;
Meneton, Pierre ;
Lakatta, Edward G. ;
Scuteri, Angelo ;
Schlessinger, David ;
Tuomilehto, Jaakko ;
Collins, Francis S. ;
Groop, Leif ;
Altshuler, David .
NATURE GENETICS, 2009, 41 (01) :56-65
[5]   The human genome browser at UCSC [J].
Kent, WJ ;
Sugnet, CW ;
Furey, TS ;
Roskin, KM ;
Pringle, TH ;
Zahler, AM ;
Haussler, D .
GENOME RESEARCH, 2002, 12 (06) :996-1006
[6]   Common variants near MC4R are associated with fat mass, weight and risk of obesity [J].
Loos, Ruth J. F. ;
Lindgren, Cecilia M. ;
Li, Shengxu ;
Wheeler, Eleanor ;
Zhao, Jing Hua ;
Prokopenko, Inga ;
Inouye, Michael ;
Freathy, Rachel M. ;
Attwood, Antony P. ;
Beckmann, Jacques S. ;
Berndt, Sonja I. ;
Bergmann, Sven ;
Bennett, Amanda J. ;
Bingham, Sheila A. ;
Bochud, Murielle ;
Brown, Morris ;
Cauchi, Stephane ;
Connell, John M. ;
Cooper, Cyrus ;
Smith, George Davey ;
Day, Ian ;
Dina, Christian ;
De, Subhajyoti ;
Dermitzakis, Emmanouil T. ;
Doney, Alex S. F. ;
Elliott, Katherine S. ;
Elliott, Paul ;
Evans, David M. ;
Farooqi, I. Sadaf ;
Froguel, Philippe ;
Ghori, Jilur ;
Groves, Christopher J. ;
Gwilliam, Rhian ;
Hadley, David ;
Hall, Alistair S. ;
Hattersley, Andrew T. ;
Hebebrand, Johannes ;
Heid, Iris M. ;
Herrera, Blanca ;
Hinney, Anke ;
Hunt, Sarah E. ;
Jarvelin, Marjo-Riitta ;
Johnson, Toby ;
Jolley, Jennifer D. M. ;
Karpe, Fredrik ;
Keniry, Andrew ;
Khaw, Kay-Tee ;
Luben, Robert N. ;
Mangino, Massimo ;
Marchini, Jonathan .
NATURE GENETICS, 2008, 40 (06) :768-775
[7]   Finding the missing heritability of complex diseases [J].
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. .
NATURE, 2009, 461 (7265) :747-753
[8]   CandiSNPer: a web tool for the identification of candidate SNPs for causal variants [J].
Schmitt, Armin O. ;
Assmus, Jens ;
Bortfeldt, Ralf H. ;
Brockmann, Gudrun A. .
BIOINFORMATICS, 2010, 26 (07) :969-970