Literature DB >> 33161601

Novel score test to increase power in association test by integrating external controls.

Yatong Li1, Seunggeun Lee1,2.   

Abstract

Recent advances in genotyping and sequencing technologies have enabled genetic association studies to leverage high-quality genotyped data to identify variants accounting for a substantial portion of disease risk. The usage of external controls, whose genomes have already been genotyped and are publicly available, could be a cost-effective approach to increase the power of association testing. There has been recent effort to integrate external controls while adjusting for possible batch effects, such as the integrating External Controls into Association Test (iECAT). The original iECAT test, however, cannot adjust for covariates such as age, gender, and so forth. Hence, based on the insight of iECAT, we propose a novel score-based test that allows for covariate adjustment and constructs a shrinkage score statistic that is a weighted sum of the score statistics using exclusively internal samples and uses both internal and external control samples. We assess the existence of batch effect at a variant by comparing control samples of internal and external sources. We show by simulation studies that our method has increased power over the original iECAT while controlling for type I error rates. We present the application of our method to the association studies of age-related macular degeneration (AMD) utilizing data from the International AMD Genomics Consortium and Michigan Genomics Initiative. Through the incorporation of the score test approach, we extend the use of iECAT to adjust for covariates and improve power, further honing the statistical methods needed to identify disease-causing variants within the human genome.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  GWAS; case-control study; external controls; saddlepoint approximation

Mesh:

Year:  2020        PMID: 33161601      PMCID: PMC9424128          DOI: 10.1002/gepi.22370

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.344


  27 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.  Variation near complement factor I is associated with risk of advanced AMD.

Authors:  Jesen A Fagerness; Julian B Maller; Benjamin M Neale; Robyn C Reynolds; Mark J Daly; Johanna M Seddon
Journal:  Eur J Hum Genet       Date:  2008-08-06       Impact factor: 4.246

3.  Rare-variant association testing for sequencing data with the sequence kernel association test.

Authors:  Michael C Wu; Seunggeun Lee; Tianxi Cai; Yun Li; Michael Boehnke; Xihong Lin
Journal:  Am J Hum Genet       Date:  2011-07-07       Impact factor: 11.025

4.  UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.

Authors:  Zhangchen Zhao; Wenjian Bi; Wei Zhou; Peter VandeHaar; Lars G Fritsche; Seunggeun Lee
Journal:  Am J Hum Genet       Date:  2019-12-19       Impact factor: 11.025

5.  Improving power for rare-variant tests by integrating external controls.

Authors:  Seunggeun Lee; Sehee Kim; Christian Fuchsberger
Journal:  Genet Epidemiol       Date:  2017-06-28       Impact factor: 2.135

6.  Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies.

Authors:  Weihua Guan; Liming Liang; Michael Boehnke; Gonçalo R Abecasis
Journal:  Genet Epidemiol       Date:  2009-09       Impact factor: 2.135

7.  Fast and robust ancestry prediction using principal component analysis.

Authors:  Daiwei Zhang; Rounak Dey; Seunggeun Lee
Journal:  Bioinformatics       Date:  2020-06-01       Impact factor: 6.937

8.  A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.

Authors:  Lars G Fritsche; Wilmar Igl; Jessica N Cooke Bailey; Felix Grassmann; Sebanti Sengupta; Jennifer L Bragg-Gresham; Kathryn P Burdon; Scott J Hebbring; Cindy Wen; Mathias Gorski; Ivana K Kim; David Cho; Donald Zack; Eric Souied; Hendrik P N Scholl; Elisa Bala; Kristine E Lee; David J Hunter; Rebecca J Sardell; Paul Mitchell; Joanna E Merriam; Valentina Cipriani; Joshua D Hoffman; Tina Schick; Yara T E Lechanteur; Robyn H Guymer; Matthew P Johnson; Yingda Jiang; Chloe M Stanton; Gabriëlle H S Buitendijk; Xiaowei Zhan; Alan M Kwong; Alexis Boleda; Matthew Brooks; Linn Gieser; Rinki Ratnapriya; Kari E Branham; Johanna R Foerster; John R Heckenlively; Mohammad I Othman; Brendan J Vote; Helena Hai Liang; Emmanuelle Souzeau; Ian L McAllister; Timothy Isaacs; Janette Hall; Stewart Lake; David A Mackey; Ian J Constable; Jamie E Craig; Terrie E Kitchner; Zhenglin Yang; Zhiguang Su; Hongrong Luo; Daniel Chen; Hong Ouyang; Ken Flagg; Danni Lin; Guanping Mao; Henry Ferreyra; Klaus Stark; Claudia N von Strachwitz; Armin Wolf; Caroline Brandl; Guenther Rudolph; Matthias Olden; Margaux A Morrison; Denise J Morgan; Matthew Schu; Jeeyun Ahn; Giuliana Silvestri; Evangelia E Tsironi; Kyu Hyung Park; Lindsay A Farrer; Anton Orlin; Alexander Brucker; Mingyao Li; Christine A Curcio; Saddek Mohand-Saïd; José-Alain Sahel; Isabelle Audo; Mustapha Benchaboune; Angela J Cree; Christina A Rennie; Srinivas V Goverdhan; Michelle Grunin; Shira Hagbi-Levi; Peter Campochiaro; Nicholas Katsanis; Frank G Holz; Frédéric Blond; Hélène Blanché; Jean-François Deleuze; Robert P Igo; Barbara Truitt; Neal S Peachey; Stacy M Meuer; Chelsea E Myers; Emily L Moore; Ronald Klein; Michael A Hauser; Eric A Postel; Monique D Courtenay; Stephen G Schwartz; Jaclyn L Kovach; William K Scott; Gerald Liew; Ava G Tan; Bamini Gopinath; John C Merriam; R Theodore Smith; Jane C Khan; Humma Shahid; Anthony T Moore; J Allie McGrath; Reneé Laux; Milam A Brantley; Anita Agarwal; Lebriz Ersoy; Albert Caramoy; Thomas Langmann; Nicole T M Saksens; Eiko K de Jong; Carel B Hoyng; Melinda S Cain; Andrea J Richardson; Tammy M Martin; John Blangero; Daniel E Weeks; Bal Dhillon; Cornelia M van Duijn; Kimberly F Doheny; Jane Romm; Caroline C W Klaver; Caroline Hayward; Michael B Gorin; Michael L Klein; Paul N Baird; Anneke I den Hollander; Sascha Fauser; John R W Yates; Rando Allikmets; Jie Jin Wang; Debra A Schaumberg; Barbara E K Klein; Stephanie A Hagstrom; Itay Chowers; Andrew J Lotery; Thierry Léveillard; Kang Zhang; Murray H Brilliant; Alex W Hewitt; Anand Swaroop; Emily Y Chew; Margaret A Pericak-Vance; Margaret DeAngelis; Dwight Stambolian; Jonathan L Haines; Sudha K Iyengar; Bernhard H F Weber; Gonçalo R Abecasis; Iris M Heid
Journal:  Nat Genet       Date:  2015-12-21       Impact factor: 38.330

9.  ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls.

Authors:  Audrey E Hendricks; Stephen C Billups; Hamish N C Pike; I Sadaf Farooqi; Eleftheria Zeggini; Stephanie A Santorico; Inês Barroso; Josée Dupuis
Journal:  PLoS Genet       Date:  2018-10-16       Impact factor: 5.917

10.  Three new genetic loci (R1210C in CFH, variants in COL8A1 and RAD51B) are independently related to progression to advanced macular degeneration.

Authors:  Johanna M Seddon; Robyn Reynolds; Yi Yu; Bernard Rosner
Journal:  PLoS One       Date:  2014-01-31       Impact factor: 3.240

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  5 in total

Review 1.  Opportunities and challenges for the use of common controls in sequencing studies.

Authors:  Genevieve L Wojcik; Jessica Murphy; Jacob L Edelson; Christopher R Gignoux; Alexander G Ioannidis; Alisa Manning; Manuel A Rivas; Steven Buyske; Audrey E Hendricks
Journal:  Nat Rev Genet       Date:  2022-05-17       Impact factor: 59.581

2.  Integrating external controls in case-control studies improves power for rare-variant tests.

Authors:  Yatong Li; Seunggeun Lee
Journal:  Genet Epidemiol       Date:  2022-02-16       Impact factor: 2.344

3.  Summix: A method for detecting and adjusting for population structure in genetic summary data.

Authors:  Ian S Arriaga-MacKenzie; Gregory Matesi; Samuel Chen; Alexandria Ronco; Katie M Marker; Jordan R Hall; Ryan Scherenberg; Mobin Khajeh-Sharafabadi; Yinfei Wu; Christopher R Gignoux; Megan Null; Audrey E Hendricks
Journal:  Am J Hum Genet       Date:  2021-06-21       Impact factor: 11.025

4.  A data harmonization pipeline to leverage external controls and boost power in GWAS.

Authors:  Danfeng Chen; Katherine Tashman; Duncan S Palmer; Benjamin Neale; Kathryn Roeder; Alex Bloemendal; Claire Churchhouse; Zheng Tracy Ke
Journal:  Hum Mol Genet       Date:  2022-02-03       Impact factor: 5.121

5.  Association between Paraoxonase-1 p.Q192R Polymorphism and Coronary Artery Disease susceptibility in the Colombian Population.

Authors:  David Corredor-Orlandelli; Santiago Sambracos-Parrado; Santiago Mantilla-García; Josué Tovar-Tirado; Valentina Vega-Ramírez; Santiago David Mendoza-Ayús; Laura Catalina Peña; María Fernanda Leal; Juliana Rodríguez-Carrillo; Juanita León-Torres; Juan Mauricio Pardo-Oviedo; Katherine Parra Abaunza; Nora Contreras Contreras Bravo; Oscar Ortega-Recalde; Dora Janeth Fonseca Mendoza
Journal:  Vasc Health Risk Manag       Date:  2021-11-03
  5 in total

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