Literature DB >> 31768069

A resource-efficient tool for mixed model association analysis of large-scale data.

Longda Jiang1, Zhili Zheng1,2, Ting Qi1, Kathryn E Kemper1, Naomi R Wray1,3, Peter M Visscher1, Jian Yang4,5.   

Abstract

The genome-wide association study (GWAS) has been widely used as an experimental design to detect associations between genetic variants and a phenotype. Two major confounding factors, population stratification and relatedness, could potentially lead to inflated GWAS test statistics and hence to spurious associations. Mixed linear model (MLM)-based approaches can be used to account for sample structure. However, genome-wide association (GWA) analyses in biobank samples such as the UK Biobank (UKB) often exceed the capability of most existing MLM-based tools especially if the number of traits is large. Here, we develop an MLM-based tool (fastGWA) that controls for population stratification by principal components and for relatedness by a sparse genetic relationship matrix for GWA analyses of biobank-scale data. We demonstrate by extensive simulations that fastGWA is reliable, robust and highly resource-efficient. We then apply fastGWA to 2,173 traits on array-genotyped and imputed samples from 456,422 individuals and to 2,048 traits on whole-exome-sequenced samples from 46,191 individuals in the UKB.

Mesh:

Year:  2019        PMID: 31768069     DOI: 10.1038/s41588-019-0530-8

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  52 in total

1.  Complement factor H polymorphism in age-related macular degeneration.

Authors:  Robert J Klein; Caroline Zeiss; Emily Y Chew; Jen-Yue Tsai; Richard S Sackler; Chad Haynes; Alice K Henning; John Paul SanGiovanni; Shrikant M Mane; Susan T Mayne; Michael B Bracken; Frederick L Ferris; Jurg Ott; Colin Barnstable; Josephine Hoh
Journal:  Science       Date:  2005-03-10       Impact factor: 47.728

2.  A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

Authors:  David J Hunter; Peter Kraft; Kevin B Jacobs; David G Cox; Meredith Yeager; Susan E Hankinson; Sholom Wacholder; Zhaoming Wang; Robert Welch; Amy Hutchinson; Junwen Wang; Kai Yu; Nilanjan Chatterjee; Nick Orr; Walter C Willett; Graham A Colditz; Regina G Ziegler; Christine D Berg; Saundra S Buys; Catherine A McCarty; Heather Spencer Feigelson; Eugenia E Calle; Michael J Thun; Richard B Hayes; Margaret Tucker; Daniela S Gerhard; Joseph F Fraumeni; Robert N Hoover; Gilles Thomas; Stephen J Chanock
Journal:  Nat Genet       Date:  2007-05-27       Impact factor: 38.330

3.  HTRA1 promoter polymorphism in wet age-related macular degeneration.

Authors:  Andrew Dewan; Mugen Liu; Stephen Hartman; Samuel Shao-Min Zhang; David T L Liu; Connie Zhao; Pancy O S Tam; Wai Man Chan; Dennis S C Lam; Michael Snyder; Colin Barnstable; Chi Pui Pang; Josephine Hoh
Journal:  Science       Date:  2006-10-19       Impact factor: 47.728

4.  Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

Authors:  Kazuki Yasuda; Kazuaki Miyake; Yukio Horikawa; Kazuo Hara; Haruhiko Osawa; Hiroto Furuta; Yushi Hirota; Hiroyuki Mori; Anna Jonsson; Yoshifumi Sato; Kazuya Yamagata; Yoshinori Hinokio; He-Yao Wang; Toshihito Tanahashi; Naoto Nakamura; Yoshitomo Oka; Naoko Iwasaki; Yasuhiko Iwamoto; Yuichiro Yamada; Yutaka Seino; Hiroshi Maegawa; Atsunori Kashiwagi; Jun Takeda; Eiichi Maeda; Hyoung Doo Shin; Young Min Cho; Kyong Soo Park; Hong Kyu Lee; Maggie C Y Ng; Ronald C W Ma; Wing-Yee So; Juliana C N Chan; Valeriya Lyssenko; Tiinamaija Tuomi; Peter Nilsson; Leif Groop; Naoyuki Kamatani; Akihiro Sekine; Yusuke Nakamura; Ken Yamamoto; Teruhiko Yoshida; Katsushi Tokunaga; Mitsuo Itakura; Hideichi Makino; Kishio Nanjo; Takashi Kadowaki; Masato Kasuga
Journal:  Nat Genet       Date:  2008-09       Impact factor: 38.330

5.  SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.

Authors:  Hiroyuki Unoki; Atsushi Takahashi; Takahisa Kawaguchi; Kazuo Hara; Momoko Horikoshi; Gitte Andersen; Daniel P K Ng; Johan Holmkvist; Knut Borch-Johnsen; Torben Jørgensen; Annelli Sandbaek; Torsten Lauritzen; Torben Hansen; Siti Nurbaya; Tatsuhiko Tsunoda; Michiaki Kubo; Tetsuya Babazono; Hiroshi Hirose; Matsuhiko Hayashi; Yasuhiko Iwamoto; Atsunori Kashiwagi; Kohei Kaku; Ryuzo Kawamori; E Shyong Tai; Oluf Pedersen; Naoyuki Kamatani; Takashi Kadowaki; Ryuichi Kikkawa; Yusuke Nakamura; Shiro Maeda
Journal:  Nat Genet       Date:  2008-09       Impact factor: 38.330

Review 6.  10 Years of GWAS Discovery: Biology, Function, and Translation.

Authors:  Peter M Visscher; Naomi R Wray; Qian Zhang; Pamela Sklar; Mark I McCarthy; Matthew A Brown; Jian Yang
Journal:  Am J Hum Genet       Date:  2017-07-06       Impact factor: 11.025

7.  A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.

Authors:  Timothy M Frayling; Nicholas J Timpson; Michael N Weedon; Eleftheria Zeggini; Rachel M Freathy; Cecilia M Lindgren; John R B Perry; Katherine S Elliott; Hana Lango; Nigel W Rayner; Beverley Shields; Lorna W Harries; Jeffrey C Barrett; Sian Ellard; Christopher J Groves; Bridget Knight; Ann-Marie Patch; Andrew R Ness; Shah Ebrahim; Debbie A Lawlor; Susan M Ring; Yoav Ben-Shlomo; Marjo-Riitta Jarvelin; Ulla Sovio; Amanda J Bennett; David Melzer; Luigi Ferrucci; Ruth J F Loos; Inês Barroso; Nicholas J Wareham; Fredrik Karpe; Katharine R Owen; Lon R Cardon; Mark Walker; Graham A Hitman; Colin N A Palmer; Alex S F Doney; Andrew D Morris; George Davey Smith; Andrew T Hattersley; Mark I McCarthy
Journal:  Science       Date:  2007-04-12       Impact factor: 47.728

8.  A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

Authors:  Laura J Scott; Karen L Mohlke; Lori L Bonnycastle; Cristen J Willer; Yun Li; William L Duren; Michael R Erdos; Heather M Stringham; Peter S Chines; Anne U Jackson; Ludmila Prokunina-Olsson; Chia-Jen Ding; Amy J Swift; Narisu Narisu; Tianle Hu; Randall Pruim; Rui Xiao; Xiao-Yi Li; Karen N Conneely; Nancy L Riebow; Andrew G Sprau; Maurine Tong; Peggy P White; Kurt N Hetrick; Michael W Barnhart; Craig W Bark; Janet L Goldstein; Lee Watkins; Fang Xiang; Jouko Saramies; Thomas A Buchanan; Richard M Watanabe; Timo T Valle; Leena Kinnunen; Gonçalo R Abecasis; Elizabeth W Pugh; Kimberly F Doheny; Richard N Bergman; Jaakko Tuomilehto; Francis S Collins; Michael Boehnke
Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

9.  Common variants in the GDF5-UQCC region are associated with variation in human height.

Authors:  Serena Sanna; Anne U Jackson; Ramaiah Nagaraja; Cristen J Willer; Wei-Min Chen; Lori L Bonnycastle; Haiqing Shen; Nicholas Timpson; Guillaume Lettre; Gianluca Usala; Peter S Chines; Heather M Stringham; Laura J Scott; Mariano Dei; Sandra Lai; Giuseppe Albai; Laura Crisponi; Silvia Naitza; Kimberly F Doheny; Elizabeth W Pugh; Yoav Ben-Shlomo; Shah Ebrahim; Debbie A Lawlor; Richard N Bergman; Richard M Watanabe; Manuela Uda; Jaakko Tuomilehto; Josef Coresh; Joel N Hirschhorn; Alan R Shuldiner; David Schlessinger; Francis S Collins; George Davey Smith; Eric Boerwinkle; Antonio Cao; Michael Boehnke; Gonçalo R Abecasis; Karen L Mohlke
Journal:  Nat Genet       Date:  2008-01-13       Impact factor: 38.330

10.  The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.

Authors:  Annalisa Buniello; Jacqueline A L MacArthur; Maria Cerezo; Laura W Harris; James Hayhurst; Cinzia Malangone; Aoife McMahon; Joannella Morales; Edward Mountjoy; Elliot Sollis; Daniel Suveges; Olga Vrousgou; Patricia L Whetzel; Ridwan Amode; Jose A Guillen; Harpreet S Riat; Stephen J Trevanion; Peggy Hall; Heather Junkins; Paul Flicek; Tony Burdett; Lucia A Hindorff; Fiona Cunningham; Helen Parkinson
Journal:  Nucleic Acids Res       Date:  2019-01-08       Impact factor: 16.971

View more
  72 in total

1.  Common variants contribute to intrinsic human brain functional networks.

Authors:  Bingxin Zhao; Tengfei Li; Stephen M Smith; Di Xiong; Xifeng Wang; Yue Yang; Tianyou Luo; Ziliang Zhu; Yue Shan; Nana Matoba; Quan Sun; Yuchen Yang; Mads E Hauberg; Jaroslav Bendl; John F Fullard; Panagiotis Roussos; Weili Lin; Yun Li; Jason L Stein; Hongtu Zhu
Journal:  Nat Genet       Date:  2022-04-07       Impact factor: 38.330

Review 2.  Navigating the pitfalls of applying machine learning in genomics.

Authors:  Sean Whalen; Jacob Schreiber; William S Noble; Katherine S Pollard
Journal:  Nat Rev Genet       Date:  2021-11-26       Impact factor: 53.242

3.  A generalized linear mixed model association tool for biobank-scale data.

Authors:  Longda Jiang; Zhili Zheng; Hailing Fang; Jian Yang
Journal:  Nat Genet       Date:  2021-11-04       Impact factor: 38.330

4.  REHE: Fast variance components estimation for linear mixed models.

Authors:  Kun Yue; Jing Ma; Timothy Thornton; Ali Shojaie
Journal:  Genet Epidemiol       Date:  2021-10-17       Impact factor: 2.135

5.  Multi-scale inference of genetic trait architecture using biologically annotated neural networks.

Authors:  Pinar Demetci; Wei Cheng; Gregory Darnell; Xiang Zhou; Sohini Ramachandran; Lorin Crawford
Journal:  PLoS Genet       Date:  2021-08-19       Impact factor: 5.917

6.  Including diverse and admixed populations in genetic epidemiology research.

Authors:  Amke Caliebe; Fasil Tekola-Ayele; Burcu F Darst; Xuexia Wang; Yeunjoo E Song; Jiang Gui; Ronnie A Sebro; David J Balding; Mohamad Saad; Marie-Pierre Dubé
Journal:  Genet Epidemiol       Date:  2022-07-16       Impact factor: 2.344

7.  Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing.

Authors:  Thomas R Austin; Caitlin P McHugh; Jennifer A Brody; Joshua C Bis; Colleen M Sitlani; Traci M Bartz; Mary L Biggs; Nisha Bansal; Petra Buzkova; Steven A Carr; Christopher R deFilippi; Mitchell S V Elkind; Howard A Fink; James S Floyd; Alison E Fohner; Robert E Gerszten; Susan R Heckbert; Daniel H Katz; Jorge R Kizer; Rozenn N Lemaitre; W T Longstreth; Barbara McKnight; Hao Mei; Kenneth J Mukamal; Anne B Newman; Debby Ngo; Michelle C Odden; Ramachandran S Vasan; Ali Shojaie; Noah Simon; George Davey Smith; Neil M Davies; David S Siscovick; Nona Sotoodehnia; Russell P Tracy; Kerri L Wiggins; Jie Zheng; Bruce M Psaty
Journal:  Eur J Epidemiol       Date:  2022-07-05       Impact factor: 12.434

8.  The genetic architecture of human complex phenotypes is modulated by linkage disequilibrium and heterozygosity.

Authors:  Dominic Holland; Oleksandr Frei; Rahul Desikan; Chun-Chieh Fan; Alexey A Shadrin; Olav B Smeland; Ole A Andreassen; Anders M Dale
Journal:  Genetics       Date:  2021-03-31       Impact factor: 4.562

9.  Reconstructing Genotypes in Private Genomic Databases from Genetic Risk Scores.

Authors:  Brooks Paige; James Bell; Aurélien Bellet; Adrià Gascón; Daphne Ezer
Journal:  J Comput Biol       Date:  2021-01-05       Impact factor: 1.479

10.  Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.

Authors:  Kira J Stanzick; Yong Li; Pascal Schlosser; Mathias Gorski; Matthias Wuttke; Laurent F Thomas; Humaira Rasheed; Bryce X Rowan; Sarah E Graham; Brett R Vanderweff; Snehal B Patil; Cassiane Robinson-Cohen; John M Gaziano; Christopher J O'Donnell; Cristen J Willer; Stein Hallan; Bjørn Olav Åsvold; Andre Gessner; Adriana M Hung; Cristian Pattaro; Anna Köttgen; Klaus J Stark; Iris M Heid; Thomas W Winkler
Journal:  Nat Commun       Date:  2021-07-16       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.