Literature DB >> 24711653

Covariate-modulated local false discovery rate for genome-wide association studies.

Rong W Zablocki1, Andrew J Schork1, Richard A Levine1, Ole A Andreassen1, Anders M Dale2, Wesley K Thompson1.   

Abstract

MOTIVATION: Genome-wide association studies (GWAS) have largely failed to identify most of the genetic basis of highly heritable diseases and complex traits. Recent work has suggested this could be because many genetic variants, each with individually small effects, compose their genetic architecture, limiting the power of GWAS, given currently obtainable sample sizes. In this scenario, Bonferroni-derived thresholds are severely underpowered to detect the vast majority of associations. Local false discovery rate (fdr) methods provide more power to detect non-null associations, but implicit assumptions about the exchangeability of single nucleotide polymorphisms (SNPs) limit their ability to discover non-null loci.
METHODS: We propose a novel covariate-modulated local false discovery rate (cmfdr) that incorporates prior information about gene element-based functional annotations of SNPs, so that SNPs from categories enriched for non-null associations have a lower fdr for a given value of a test statistic than SNPs in unenriched categories. This readjustment of fdr based on functional annotations is achieved empirically by fitting a covariate-modulated parametric two-group mixture model. The proposed cmfdr methodology is applied to a large Crohn's disease GWAS.
RESULTS: Use of cmfdr dramatically improves power, e.g. increasing the number of loci declared significant at the 0.05 fdr level by a factor of 5.4. We also demonstrate that SNPs were declared significant using cmfdr compared with usual fdr replicate in much higher numbers, while maintaining similar replication rates for a given fdr cutoff in de novo samples, using the eight Crohn's disease substudies as independent training and test datasets. Availability an implementation: https://sites.google.com/site/covmodfdr/ CONTACT: : wes.stat@gmail.com SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Mesh:

Year:  2014        PMID: 24711653      PMCID: PMC4103587          DOI: 10.1093/bioinformatics/btu145

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  26 in total

1.  Has the revolution arrived?

Authors:  Francis Collins
Journal:  Nature       Date:  2010-04-01       Impact factor: 49.962

Review 2.  Annotating individual human genomes.

Authors:  Ali Torkamani; Ashley A Scott-Van Zeeland; Eric J Topol; Nicholas J Schork
Journal:  Genomics       Date:  2011-08-02       Impact factor: 5.736

3.  Common SNPs explain a large proportion of the heritability for human height.

Authors:  Jian Yang; Beben Benyamin; Brian P McEvoy; Scott Gordon; Anjali K Henders; Dale R Nyholt; Pamela A Madden; Andrew C Heath; Nicholas G Martin; Grant W Montgomery; Michael E Goddard; Peter M Visscher
Journal:  Nat Genet       Date:  2010-06-20       Impact factor: 38.330

4.  Genome partitioning of genetic variation for complex traits using common SNPs.

Authors:  Jian Yang; Teri A Manolio; Louis R Pasquale; Eric Boerwinkle; Neil Caporaso; Julie M Cunningham; Mariza de Andrade; Bjarke Feenstra; Eleanor Feingold; M Geoffrey Hayes; William G Hill; Maria Teresa Landi; Alvaro Alonso; Guillaume Lettre; Peng Lin; Hua Ling; William Lowe; Rasika A Mathias; Mads Melbye; Elizabeth Pugh; Marilyn C Cornelis; Bruce S Weir; Michael E Goddard; Peter M Visscher
Journal:  Nat Genet       Date:  2011-05-08       Impact factor: 38.330

5.  Recent insights into the genetics of inflammatory bowel disease.

Authors:  Judy H Cho; Steven R Brant
Journal:  Gastroenterology       Date:  2011-05       Impact factor: 22.682

6.  Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.

Authors:  Andre Franke; Dermot P B McGovern; Jeffrey C Barrett; Kai Wang; Graham L Radford-Smith; Tariq Ahmad; Charlie W Lees; Tobias Balschun; James Lee; Rebecca Roberts; Carl A Anderson; Joshua C Bis; Suzanne Bumpstead; David Ellinghaus; Eleonora M Festen; Michel Georges; Todd Green; Talin Haritunians; Luke Jostins; Anna Latiano; Christopher G Mathew; Grant W Montgomery; Natalie J Prescott; Soumya Raychaudhuri; Jerome I Rotter; Philip Schumm; Yashoda Sharma; Lisa A Simms; Kent D Taylor; David Whiteman; Cisca Wijmenga; Robert N Baldassano; Murray Barclay; Theodore M Bayless; Stephan Brand; Carsten Büning; Albert Cohen; Jean-Frederick Colombel; Mario Cottone; Laura Stronati; Ted Denson; Martine De Vos; Renata D'Inca; Marla Dubinsky; Cathryn Edwards; Tim Florin; Denis Franchimont; Richard Gearry; Jürgen Glas; Andre Van Gossum; Stephen L Guthery; Jonas Halfvarson; Hein W Verspaget; Jean-Pierre Hugot; Amir Karban; Debby Laukens; Ian Lawrance; Marc Lemann; Arie Levine; Cecile Libioulle; Edouard Louis; Craig Mowat; William Newman; Julián Panés; Anne Phillips; Deborah D Proctor; Miguel Regueiro; Richard Russell; Paul Rutgeerts; Jeremy Sanderson; Miquel Sans; Frank Seibold; A Hillary Steinhart; Pieter C F Stokkers; Leif Torkvist; Gerd Kullak-Ublick; David Wilson; Thomas Walters; Stephan R Targan; Steven R Brant; John D Rioux; Mauro D'Amato; Rinse K Weersma; Subra Kugathasan; Anne M Griffiths; John C Mansfield; Severine Vermeire; Richard H Duerr; Mark S Silverberg; Jack Satsangi; Stefan Schreiber; Judy H Cho; Vito Annese; Hakon Hakonarson; Mark J Daly; Miles Parkes
Journal:  Nat Genet       Date:  2010-12       Impact factor: 38.330

7.  Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors.

Authors:  Ole A Andreassen; Srdjan Djurovic; Wesley K Thompson; Andrew J Schork; Kenneth S Kendler; Michael C O'Donovan; Dan Rujescu; Thomas Werge; Martijn van de Bunt; Andrew P Morris; Mark I McCarthy; J Cooper Roddey; Linda K McEvoy; Rahul S Desikan; Anders M Dale
Journal:  Am J Hum Genet       Date:  2013-01-31       Impact factor: 11.025

8.  Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.

Authors:  Erin N Smith; Daniel L Koller; Corrie Panganiban; Szabolcs Szelinger; Peng Zhang; Judith A Badner; Thomas B Barrett; Wade H Berrettini; Cinnamon S Bloss; William Byerley; William Coryell; Howard J Edenberg; Tatiana Foroud; Elliot S Gershon; Tiffany A Greenwood; Yiran Guo; Maria Hipolito; Brendan J Keating; William B Lawson; Chunyu Liu; Pamela B Mahon; Melvin G McInnis; Francis J McMahon; Rebecca McKinney; Sarah S Murray; Caroline M Nievergelt; John I Nurnberger; Evaristus A Nwulia; James B Potash; John Rice; Thomas G Schulze; William A Scheftner; Paul D Shilling; Peter P Zandi; Sebastian Zöllner; David W Craig; Nicholas J Schork; John R Kelsoe
Journal:  PLoS Genet       Date:  2011-06-30       Impact factor: 5.917

9.  Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.

Authors:  Carl A Anderson; Gabrielle Boucher; Charlie W Lees; Andre Franke; Mauro D'Amato; Kent D Taylor; James C Lee; Philippe Goyette; Marcin Imielinski; Anna Latiano; Caroline Lagacé; Regan Scott; Leila Amininejad; Suzannah Bumpstead; Leonard Baidoo; Robert N Baldassano; Murray Barclay; Theodore M Bayless; Stephan Brand; Carsten Büning; Jean-Frédéric Colombel; Lee A Denson; Martine De Vos; Marla Dubinsky; Cathryn Edwards; David Ellinghaus; Rudolf S N Fehrmann; James A B Floyd; Timothy Florin; Denis Franchimont; Lude Franke; Michel Georges; Jürgen Glas; Nicole L Glazer; Stephen L Guthery; Talin Haritunians; Nicholas K Hayward; Jean-Pierre Hugot; Gilles Jobin; Debby Laukens; Ian Lawrance; Marc Lémann; Arie Levine; Cecile Libioulle; Edouard Louis; Dermot P McGovern; Monica Milla; Grant W Montgomery; Katherine I Morley; Craig Mowat; Aylwin Ng; William Newman; Roel A Ophoff; Laura Papi; Orazio Palmieri; Laurent Peyrin-Biroulet; Julián Panés; Anne Phillips; Natalie J Prescott; Deborah D Proctor; Rebecca Roberts; Richard Russell; Paul Rutgeerts; Jeremy Sanderson; Miquel Sans; Philip Schumm; Frank Seibold; Yashoda Sharma; Lisa A Simms; Mark Seielstad; A Hillary Steinhart; Stephan R Targan; Leonard H van den Berg; Morten Vatn; Hein Verspaget; Thomas Walters; Cisca Wijmenga; David C Wilson; Harm-Jan Westra; Ramnik J Xavier; Zhen Z Zhao; Cyriel Y Ponsioen; Vibeke Andersen; Leif Torkvist; Maria Gazouli; Nicholas P Anagnou; Tom H Karlsen; Limas Kupcinskas; Jurgita Sventoraityte; John C Mansfield; Subra Kugathasan; Mark S Silverberg; Jonas Halfvarson; Jerome I Rotter; Christopher G Mathew; Anne M Griffiths; Richard Gearry; Tariq Ahmad; Steven R Brant; Mathias Chamaillard; Jack Satsangi; Judy H Cho; Stefan Schreiber; Mark J Daly; Jeffrey C Barrett; Miles Parkes; Vito Annese; Hakon Hakonarson; Graham Radford-Smith; Richard H Duerr; Séverine Vermeire; Rinse K Weersma; John D Rioux
Journal:  Nat Genet       Date:  2011-02-06       Impact factor: 38.330

10.  An integrated encyclopedia of DNA elements in the human genome.

Authors: 
Journal:  Nature       Date:  2012-09-06       Impact factor: 49.962

View more
  18 in total

1.  Leveraging Multi-ethnic Evidence for Mapping Complex Traits in Minority Populations: An Empirical Bayes Approach.

Authors:  Marc A Coram; Sophie I Candille; Qing Duan; Kei Hang K Chan; Yun Li; Charles Kooperberg; Alex P Reiner; Hua Tang
Journal:  Am J Hum Genet       Date:  2015-04-16       Impact factor: 11.025

Review 2.  Beyond heritability: improving discoverability in imaging genetics.

Authors:  Chun Chieh Fan; Olav B Smeland; Andrew J Schork; Chi-Hua Chen; Dominic Holland; Min-Tzu Lo; V S Sundar; Oleksandr Frei; Terry L Jernigan; Ole A Andreassen; Anders M Dale
Journal:  Hum Mol Genet       Date:  2018-05-01       Impact factor: 6.150

3.  A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.

Authors:  Yu-Ru Su; Chongzhi Di; Stephanie Bien; Licai Huang; Xinyuan Dong; Goncalo Abecasis; Sonja Berndt; Stephane Bezieau; Hermann Brenner; Bette Caan; Graham Casey; Jenny Chang-Claude; Stephen Chanock; Sai Chen; Charles Connolly; Keith Curtis; Jane Figueiredo; Manish Gala; Steven Gallinger; Tabitha Harrison; Michael Hoffmeister; John Hopper; Jeroen R Huyghe; Mark Jenkins; Amit Joshi; Loic Le Marchand; Polly Newcomb; Deborah Nickerson; John Potter; Robert Schoen; Martha Slattery; Emily White; Brent Zanke; Ulrike Peters; Li Hsu
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

4.  Boosting the power of schizophrenia genetics by leveraging new statistical tools.

Authors:  Ole A Andreassen; Wesley K Thompson; Anders M Dale
Journal:  Schizophr Bull       Date:  2013-12-06       Impact factor: 9.306

5.  Genetic Markers of Human Evolution Are Enriched in Schizophrenia.

Authors:  Saurabh Srinivasan; Francesco Bettella; Morten Mattingsdal; Yunpeng Wang; Aree Witoelar; Andrew J Schork; Wesley K Thompson; Verena Zuber; Bendik S Winsvold; John-Anker Zwart; David A Collier; Rahul S Desikan; Ingrid Melle; Thomas Werge; Anders M Dale; Srdjan Djurovic; Ole A Andreassen
Journal:  Biol Psychiatry       Date:  2015-10-21       Impact factor: 13.382

6.  Weighted False Discovery Rate Control in Large-Scale Multiple Testing.

Authors:  Pallavi Basu; T Tony Cai; Kiranmoy Das; Wenguang Sun
Journal:  J Am Stat Assoc       Date:  2018-06-12       Impact factor: 5.033

7.  Covariate adaptive familywise error rate control for genome-wide association studies.

Authors:  Huijuan Zhou; Xianyang Zhang; Jun Chen
Journal:  Biometrika       Date:  2020-11-27       Impact factor: 2.445

8.  Bayesian GWAS with Structured and Non-Local Priors.

Authors:  Adam Kaplan; Eric F Lock; Mark Fiecas
Journal:  Bioinformatics       Date:  2020-01-01       Impact factor: 6.937

Review 9.  New statistical approaches exploit the polygenic architecture of schizophrenia--implications for the underlying neurobiology.

Authors:  Andrew J Schork; Yunpeng Wang; Wesley K Thompson; Anders M Dale; Ole A Andreassen
Journal:  Curr Opin Neurobiol       Date:  2015-11-08       Impact factor: 6.627

10.  Accurate error control in high-dimensional association testing using conditional false discovery rates.

Authors:  James Liley; Chris Wallace
Journal:  Biom J       Date:  2021-03-07       Impact factor: 1.715

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.