Literature DB >> 24166731

GEE-based SNP set association test for continuous and discrete traits in family-based association studies.

Xuefeng Wang1, Seunggeun Lee, Xiaofeng Zhu, Susan Redline, Xihong Lin.   

Abstract

Family-based genetic association studies of related individuals provide opportunities to detect genetic variants that complement studies of unrelated individuals. Most statistical methods for family association studies for common variants are single marker based, which test one SNP a time. In this paper, we consider testing the effect of an SNP set, e.g., SNPs in a gene, in family studies, for both continuous and discrete traits. Specifically, we propose a generalized estimating equations (GEEs) based kernel association test, a variance component based testing method, to test for the association between a phenotype and multiple variants in an SNP set jointly using family samples. The proposed approach allows for both continuous and discrete traits, where the correlation among family members is taken into account through the use of an empirical covariance estimator. We derive the theoretical distribution of the proposed statistic under the null and develop analytical methods to calculate the P-values. We also propose an efficient resampling method for correcting for small sample size bias in family studies. The proposed method allows for easily incorporating covariates and SNP-SNP interactions. Simulation studies show that the proposed method properly controls for type I error rates under both random and ascertained sampling schemes in family studies. We demonstrate through simulation studies that our approach has superior performance for association mapping compared to the single marker based minimum P-value GEE test for an SNP-set effect over a range of scenarios. We illustrate the application of the proposed method using data from the Cleveland Family GWAS Study.
© 2013 WILEY PERIODICALS, INC.

Entities:  

Keywords:  family-based association; generalized estimation equations; kernel machine regression; marginal models; score test; variance component

Mesh:

Substances:

Year:  2013        PMID: 24166731      PMCID: PMC4007511          DOI: 10.1002/gepi.21763

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  41 in total

1.  Optimal tests for rare variant effects in sequencing association studies.

Authors:  Seunggeun Lee; Michael C Wu; Xihong Lin
Journal:  Biostatistics       Date:  2012-06-14       Impact factor: 5.899

2.  Powerful SNP-set analysis for case-control genome-wide association studies.

Authors:  Michael C Wu; Peter Kraft; Michael P Epstein; Deanne M Taylor; Stephen J Chanock; David J Hunter; Xihong Lin
Journal:  Am J Hum Genet       Date:  2010-06-11       Impact factor: 11.025

3.  Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression.

Authors:  Fang Han; Wei Pan
Journal:  Genet Epidemiol       Date:  2010-11       Impact factor: 2.135

4.  Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models.

Authors:  Dawei Liu; Xihong Lin; Debashis Ghosh
Journal:  Biometrics       Date:  2007-12       Impact factor: 2.571

5.  An approximate distribution of estimates of variance components.

Authors:  F E SATTERTHWAITE
Journal:  Biometrics       Date:  1946-12       Impact factor: 2.571

6.  Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data.

Authors:  Daniel J Schaid; Shannon K McDonnell; Jason P Sinnwell; Stephen N Thibodeau
Journal:  Genet Epidemiol       Date:  2013-05-05       Impact factor: 2.135

7.  Family-based association tests for sequence data, and comparisons with population-based association tests.

Authors:  Iuliana Ionita-Laza; Seunggeun Lee; Vladimir Makarov; Joseph D Buxbaum; Xihong Lin
Journal:  Eur J Hum Genet       Date:  2013-02-06       Impact factor: 4.246

8.  Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).

Authors:  Tao Feng; Robert C Elston; Xiaofeng Zhu
Journal:  Genet Epidemiol       Date:  2011-05-18       Impact factor: 2.135

9.  Avoiding the high Bonferroni penalty in genome-wide association studies.

Authors:  Xiaoyi Gao; Lewis C Becker; Diane M Becker; Joshua D Starmer; Michael A Province
Journal:  Genet Epidemiol       Date:  2010-01       Impact factor: 2.135

10.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

Authors:  Georg B Ehret; Patricia B Munroe; Kenneth M Rice; Murielle Bochud; Andrew D Johnson; Daniel I Chasman; Albert V Smith; Martin D Tobin; Germaine C Verwoert; Shih-Jen Hwang; Vasyl Pihur; Peter Vollenweider; Paul F O'Reilly; Najaf Amin; Jennifer L Bragg-Gresham; Alexander Teumer; Nicole L Glazer; Lenore Launer; Jing Hua Zhao; Yurii Aulchenko; Simon Heath; Siim Sõber; Afshin Parsa; Jian'an Luan; Pankaj Arora; Abbas Dehghan; Feng Zhang; Gavin Lucas; Andrew A Hicks; Anne U Jackson; John F Peden; Toshiko Tanaka; Sarah H Wild; Igor Rudan; Wilmar Igl; Yuri Milaneschi; Alex N Parker; Cristiano Fava; John C Chambers; Ervin R Fox; Meena Kumari; Min Jin Go; Pim van der Harst; Wen Hong Linda Kao; Marketa Sjögren; D G Vinay; Myriam Alexander; Yasuharu Tabara; Sue Shaw-Hawkins; Peter H Whincup; Yongmei Liu; Gang Shi; Johanna Kuusisto; Bamidele Tayo; Mark Seielstad; Xueling Sim; Khanh-Dung Hoang Nguyen; Terho Lehtimäki; Giuseppe Matullo; Ying Wu; Tom R Gaunt; N Charlotte Onland-Moret; Matthew N Cooper; Carl G P Platou; Elin Org; Rebecca Hardy; Santosh Dahgam; Jutta Palmen; Veronique Vitart; Peter S Braund; Tatiana Kuznetsova; Cuno S P M Uiterwaal; Adebowale Adeyemo; Walter Palmas; Harry Campbell; Barbara Ludwig; Maciej Tomaszewski; Ioanna Tzoulaki; Nicholette D Palmer; Thor Aspelund; Melissa Garcia; Yen-Pei C Chang; Jeffrey R O'Connell; Nanette I Steinle; Diederick E Grobbee; Dan E Arking; Sharon L Kardia; Alanna C Morrison; Dena Hernandez; Samer Najjar; Wendy L McArdle; David Hadley; Morris J Brown; John M Connell; Aroon D Hingorani; Ian N M Day; Debbie A Lawlor; John P Beilby; Robert W Lawrence; Robert Clarke; Jemma C Hopewell; Halit Ongen; Albert W Dreisbach; Yali Li; J Hunter Young; Joshua C Bis; Mika Kähönen; Jorma Viikari; Linda S Adair; Nanette R Lee; Ming-Huei Chen; Matthias Olden; Cristian Pattaro; Judith A Hoffman Bolton; Anna Köttgen; Sven Bergmann; Vincent Mooser; Nish Chaturvedi; Timothy M Frayling; Muhammad Islam; Tazeen H Jafar; Jeanette Erdmann; Smita R Kulkarni; Stefan R Bornstein; Jürgen Grässler; Leif Groop; Benjamin F Voight; Johannes Kettunen; Philip Howard; Andrew Taylor; Simonetta Guarrera; Fulvio Ricceri; Valur Emilsson; Andrew Plump; Inês Barroso; Kay-Tee Khaw; Alan B Weder; Steven C Hunt; Yan V Sun; Richard N Bergman; Francis S Collins; Lori L Bonnycastle; Laura J Scott; Heather M Stringham; Leena Peltonen; Markus Perola; Erkki Vartiainen; Stefan-Martin Brand; Jan A Staessen; Thomas J Wang; Paul R Burton; Maria Soler Artigas; Yanbin Dong; Harold Snieder; Xiaoling Wang; Haidong Zhu; Kurt K Lohman; Megan E Rudock; Susan R Heckbert; Nicholas L Smith; Kerri L Wiggins; Ayo Doumatey; Daniel Shriner; Gudrun Veldre; Margus Viigimaa; Sanjay Kinra; Dorairaj Prabhakaran; Vikal Tripathy; Carl D Langefeld; Annika Rosengren; Dag S Thelle; Anna Maria Corsi; Andrew Singleton; Terrence Forrester; Gina Hilton; Colin A McKenzie; Tunde Salako; Naoharu Iwai; Yoshikuni Kita; Toshio Ogihara; Takayoshi Ohkubo; Tomonori Okamura; Hirotsugu Ueshima; Satoshi Umemura; Susana Eyheramendy; Thomas Meitinger; H-Erich Wichmann; Yoon Shin Cho; Hyung-Lae Kim; Jong-Young Lee; James Scott; Joban S Sehmi; Weihua Zhang; Bo Hedblad; Peter Nilsson; George Davey Smith; Andrew Wong; Narisu Narisu; Alena Stančáková; Leslie J Raffel; Jie Yao; Sekar Kathiresan; Christopher J O'Donnell; Stephen M Schwartz; M Arfan Ikram; W T Longstreth; Thomas H Mosley; Sudha Seshadri; Nick R G Shrine; Louise V Wain; Mario A Morken; Amy J Swift; Jaana Laitinen; Inga Prokopenko; Paavo Zitting; Jackie A Cooper; Steve E Humphries; John Danesh; Asif Rasheed; Anuj Goel; Anders Hamsten; Hugh Watkins; Stephan J L Bakker; Wiek H van Gilst; Charles S Janipalli; K Radha Mani; Chittaranjan S Yajnik; Albert Hofman; Francesco U S Mattace-Raso; Ben A Oostra; Ayse Demirkan; Aaron Isaacs; Fernando Rivadeneira; Edward G Lakatta; Marco Orru; Angelo Scuteri; Mika Ala-Korpela; Antti J Kangas; Leo-Pekka Lyytikäinen; Pasi Soininen; Taru Tukiainen; Peter Würtz; Rick Twee-Hee Ong; Marcus Dörr; Heyo K Kroemer; Uwe Völker; Henry Völzke; Pilar Galan; Serge Hercberg; Mark Lathrop; Diana Zelenika; Panos Deloukas; Massimo Mangino; Tim D Spector; Guangju Zhai; James F Meschia; Michael A Nalls; Pankaj Sharma; Janos Terzic; M V Kranthi Kumar; Matthew Denniff; Ewa Zukowska-Szczechowska; Lynne E Wagenknecht; F Gerald R Fowkes; Fadi J Charchar; Peter E H Schwarz; Caroline Hayward; Xiuqing Guo; Charles Rotimi; Michiel L Bots; Eva Brand; Nilesh J Samani; Ozren Polasek; Philippa J Talmud; Fredrik Nyberg; Diana Kuh; Maris Laan; Kristian Hveem; Lyle J Palmer; Yvonne T van der Schouw; Juan P Casas; Karen L Mohlke; Paolo Vineis; Olli Raitakari; Santhi K Ganesh; Tien Y Wong; E Shyong Tai; Richard S Cooper; Markku Laakso; Dabeeru C Rao; Tamara B Harris; Richard W Morris; Anna F Dominiczak; Mika Kivimaki; Michael G Marmot; Tetsuro Miki; Danish Saleheen; Giriraj R Chandak; Josef Coresh; Gerjan Navis; Veikko Salomaa; Bok-Ghee Han; Xiaofeng Zhu; Jaspal S Kooner; Olle Melander; Paul M Ridker; Stefania Bandinelli; Ulf B Gyllensten; Alan F Wright; James F Wilson; Luigi Ferrucci; Martin Farrall; Jaakko Tuomilehto; Peter P Pramstaller; Roberto Elosua; Nicole Soranzo; Eric J G Sijbrands; David Altshuler; Ruth J F Loos; Alan R Shuldiner; Christian Gieger; Pierre Meneton; Andre G Uitterlinden; Nicholas J Wareham; Vilmundur Gudnason; Jerome I Rotter; Rainer Rettig; Manuela Uda; David P Strachan; Jacqueline C M Witteman; Anna-Liisa Hartikainen; Jacques S Beckmann; Eric Boerwinkle; Ramachandran S Vasan; Michael Boehnke; Martin G Larson; Marjo-Riitta Järvelin; Bruce M Psaty; Gonçalo R Abecasis; Aravinda Chakravarti; Paul Elliott; Cornelia M van Duijn; Christopher Newton-Cheh; Daniel Levy; Mark J Caulfield; Toby Johnson
Journal:  Nature       Date:  2011-09-11       Impact factor: 49.962

View more
  35 in total

1.  Adaptive testing for association between two random vectors in moderate to high dimensions.

Authors:  Zhiyuan Xu; Gongjun Xu; Wei Pan
Journal:  Genet Epidemiol       Date:  2017-07-17       Impact factor: 2.135

2.  ADAPTIVE-WEIGHT BURDEN TEST FOR ASSOCIATIONS BETWEEN QUANTITATIVE TRAITS AND GENOTYPE DATA WITH COMPLEX CORRELATIONS.

Authors:  Xiaowei Wu; Ting Guan; Dajiang J Liu; Luis G León Novelo; Dipankar Bandyopadhyay
Journal:  Ann Appl Stat       Date:  2018-09-11       Impact factor: 2.083

3.  Genetic association analysis under complex survey sampling: the Hispanic Community Health Study/Study of Latinos.

Authors:  Dan-Yu Lin; Ran Tao; William D Kalsbeek; Donglin Zeng; Franklyn Gonzalez; Lindsay Fernández-Rhodes; Mariaelisa Graff; Gary G Koch; Kari E North; Gerardo Heiss
Journal:  Am J Hum Genet       Date:  2014-12-04       Impact factor: 11.025

4.  Detecting Rare Mutations with Heterogeneous Effects Using a Family-Based Genetic Random Field Method.

Authors:  Ming Li; Zihuai He; Xiaoran Tong; John S Witte; Qing Lu
Journal:  Genetics       Date:  2018-08-13       Impact factor: 4.562

5.  PopCluster: an algorithm to identify genetic variants with ethnicity-dependent effects.

Authors:  Anastasia Gurinovich; Harold Bae; John J Farrell; Stacy L Andersen; Stefano Monti; Annibale Puca; Gil Atzmon; Nir Barzilai; Thomas T Perls; Paola Sebastiani
Journal:  Bioinformatics       Date:  2019-09-01       Impact factor: 6.937

6.  Flexible and robust methods for rare-variant testing of quantitative traits in trios and nuclear families.

Authors:  Yunxuan Jiang; Karen N Conneely; Michael P Epstein
Journal:  Genet Epidemiol       Date:  2014-07-14       Impact factor: 2.135

Review 7.  Rare-variant association analysis: study designs and statistical tests.

Authors:  Seunggeung Lee; Gonçalo R Abecasis; Michael Boehnke; Xihong Lin
Journal:  Am J Hum Genet       Date:  2014-07-03       Impact factor: 11.025

8.  Boosting the Power of the Sequence Kernel Association Test by Properly Estimating Its Null Distribution.

Authors:  Kai Wang
Journal:  Am J Hum Genet       Date:  2016-06-09       Impact factor: 11.025

9.  Rare variant association test in family-based sequencing studies.

Authors:  Xuefeng Wang; Zhenyu Zhang; Nathan Morris; Tianxi Cai; Seunggeun Lee; Chaolong Wang; Timothy W Yu; Christopher A Walsh; Xihong Lin
Journal:  Brief Bioinform       Date:  2017-11-01       Impact factor: 11.622

10.  Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data.

Authors:  Zihuai He; Bin Xu; Seunggeun Lee; Iuliana Ionita-Laza
Journal:  Am J Hum Genet       Date:  2017-08-24       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.