Literature DB >> 21922539

Multilocus association testing with penalized regression.

Saonli Basu1, Wei Pan, Xiaotong Shen, William S Oetting.   

Abstract

In multilocus association analysis, since some markers may not be associated with a trait, it seems attractive to use penalized regression with the capability of automatic variable selection. On the other hand, in spite of a rapidly growing body of literature on penalized regression, most focus on variable selection and outcome prediction, for which penalized methods are generally more effective than their nonpenalized counterparts. However, for statistical inference, i.e. hypothesis testing and interval estimation, it is less clear how penalized methods would perform, or even how to best apply them, largely due to lack of studies on this topic. In our motivating data for a cohort of kidney transplant recipients, it is of primary interest to assess whether a group of genetic variants are associated with a binary clinical outcome, acute rejection at 6 months. In this article, we study some technical issues and alternative implementations of hypothesis testing in Lasso penalized logistic regression, and compare their performance with each other and with several existing global tests, some of which are specifically designed as variance component tests for high-dimensional data. The most interesting, and perhaps surprising, conclusion of this study is that, for low to moderately high-dimensional data, statistical tests based on Lasso penalized regression are not necessarily more powerful than some existing global tests. In addition, in penalized regression, rather than building a test based on a single selected "best" model, combining multiple tests, each of which is built on a candidate model, might be more promising.
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21922539      PMCID: PMC3350336          DOI: 10.1002/gepi.20625

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


  37 in total

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Journal:  Am J Hum Genet       Date:  2003-11-21       Impact factor: 11.025

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

Review 3.  Genomic similarity and kernel methods II: methods for genomic information.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

Review 4.  Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

5.  So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests.

Authors:  Karen N Conneely; Michael Boehnke
Journal:  Am J Hum Genet       Date:  2007-12       Impact factor: 11.025

6.  Accommodating linkage disequilibrium in genetic-association analyses via ridge regression.

Authors:  Nathalie Malo; Ondrej Libiger; Nicholas J Schork
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

Review 7.  The impact of immune gene polymorphisms in kidney and liver transplantation.

Authors:  Peter Nickerson
Journal:  Clin Lab Med       Date:  2008-09       Impact factor: 1.935

8.  Risk prediction using genome-wide association studies.

Authors:  Charles Kooperberg; Michael LeBlanc; Valerie Obenchain
Journal:  Genet Epidemiol       Date:  2010-11       Impact factor: 2.135

9.  HIGH DIMENSIONAL VARIABLE SELECTION.

Authors:  Larry Wasserman; Kathryn Roeder
Journal:  Ann Stat       Date:  2009-01-01       Impact factor: 4.028

10.  Analysis of North American Rheumatoid Arthritis Consortium data using a penalized logistic regression approach.

Authors:  Pascal Croiseau; Heather J Cordell
Journal:  BMC Proc       Date:  2009-12-15
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  7 in total

1.  Statistical tests for detecting associations with groups of genetic variants: generalization, evaluation, and implementation.

Authors:  John Ferguson; William Wheeler; Yiping Fu; Ludmila Prokunina-Olsson; Hongyu Zhao; Joshua Sampson
Journal:  Eur J Hum Genet       Date:  2012-10-24       Impact factor: 4.246

2.  Prioritizing genetic variants in GWAS with lasso using permutation-assisted tuning.

Authors:  Songshan Yang; Jiawei Wen; Scott T Eckert; Yaqun Wang; Dajiang J Liu; Rongling Wu; Runze Li; Xiang Zhan
Journal:  Bioinformatics       Date:  2020-06-01       Impact factor: 6.937

3.  Regularized rare variant enrichment analysis for case-control exome sequencing data.

Authors:  Nicholas B Larson; Daniel J Schaid
Journal:  Genet Epidemiol       Date:  2013-12-30       Impact factor: 2.135

4.  Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging.

Authors:  William Valdar; Jeremy Sabourin; Andrew Nobel; Christopher C Holmes
Journal:  Genet Epidemiol       Date:  2012-04-30       Impact factor: 2.135

5.  Penalized regression approaches to testing for quantitative trait-rare variant association.

Authors:  Sunkyung Kim; Wei Pan; Xiaotong Shen
Journal:  Front Genet       Date:  2014-05-13       Impact factor: 4.599

6.  On multi-marker tests for association in case-control studies.

Authors:  Margaret A Taub; Holger R Schwender; Samuel G Younkin; Thomas A Louis; Ingo Ruczinski
Journal:  Front Genet       Date:  2013-12-16       Impact factor: 4.599

7.  Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease.

Authors:  Sultan Chaudhury; Tulsi Patel; Imelda S Barber; Tamar Guetta-Baranes; Keeley J Brookes; Sally Chappell; James Turton; Rita Guerreiro; Jose Bras; Dena Hernandez; Andrew Singleton; John Hardy; David Mann; Kevin Morgan
Journal:  Neurobiol Aging       Date:  2017-10-10       Impact factor: 4.673

  7 in total

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