Literature DB >> 23386037

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

Iuliana Ionita-Laza1, Seunggeun Lee, Vladimir Makarov, Joseph D Buxbaum, Xihong Lin.   

Abstract

Recent advances in high-throughput sequencing technologies make it increasingly more efficient to sequence large cohorts for many complex traits. We discuss here a class of sequence-based association tests for family-based designs that corresponds naturally to previously proposed population-based tests, including the classical Burden and variance-component tests. This framework allows for a direct comparison between the powers of sequence-based association tests with family- vs population-based designs. We show that for dichotomous traits using family-based controls results in similar power levels as the population-based design (although at an increased sequencing cost for the family-based design), while for continuous traits (in random samples, no ascertainment) the population-based design can be substantially more powerful. A possible disadvantage of population-based designs is that they can lead to increased false-positive rates in the presence of population stratification, while the family-based designs are robust to population stratification. We show also an application to a small exome-sequencing family-based study on autism spectrum disorders. The tests are implemented in publicly available software.

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Year:  2013        PMID: 23386037      PMCID: PMC3778346          DOI: 10.1038/ejhg.2012.308

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  39 in total

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2.  Hypothesis testing in semiparametric additive mixed models.

Authors:  Daowen Zhang; Xihong Lin
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3.  The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.

Authors:  Aaron McKenna; Matthew Hanna; Eric Banks; Andrey Sivachenko; Kristian Cibulskis; Andrew Kernytsky; Kiran Garimella; David Altshuler; Stacey Gabriel; Mark Daly; Mark A DePristo
Journal:  Genome Res       Date:  2010-07-19       Impact factor: 9.043

4.  A data-adaptive sum test for disease association with multiple common or rare variants.

Authors:  Fang Han; Wei Pan
Journal:  Hum Hered       Date:  2010-04-23       Impact factor: 0.444

5.  Pooled association tests for rare variants in exon-resequencing studies.

Authors:  Alkes L Price; Gregory V Kryukov; Paul I W de Bakker; Shaun M Purcell; Jeff Staples; Lee-Jen Wei; Shamil R Sunyaev
Journal:  Am J Hum Genet       Date:  2010-05-13       Impact factor: 11.025

6.  A method for quantifying differentiation between populations at multi-allelic loci and its implications for investigating identity and paternity.

Authors:  D J Balding; R A Nichols
Journal:  Genetica       Date:  1995       Impact factor: 1.082

7.  A covering method for detecting genetic associations between rare variants and common phenotypes.

Authors:  Gaurav Bhatia; Vikas Bansal; Olivier Harismendy; Nicholas J Schork; Eric J Topol; Kelly Frazer; Vineet Bafna
Journal:  PLoS Comput Biol       Date:  2010-10-14       Impact factor: 4.475

8.  A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions.

Authors:  Dajiang J Liu; Suzanne M Leal
Journal:  PLoS Genet       Date:  2010-10-14       Impact factor: 5.917

9.  An evolutionary framework for association testing in resequencing studies.

Authors:  C Ryan King; Paul J Rathouz; Dan L Nicolae
Journal:  PLoS Genet       Date:  2010-11-11       Impact factor: 5.917

10.  A groupwise association test for rare mutations using a weighted sum statistic.

Authors:  Bo Eskerod Madsen; Sharon R Browning
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917

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  53 in total

1.  Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.

Authors:  Zongxiao He; Brian J O'Roak; Joshua D Smith; Gao Wang; Stanley Hooker; Regie Lyn P Santos-Cortez; Biao Li; Mengyuan Kan; Nik Krumm; Deborah A Nickerson; Jay Shendure; Evan E Eichler; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

2.  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

3.  A statistical approach for rare-variant association testing in affected sibships.

Authors:  Michael P Epstein; Richard Duncan; Erin B Ware; Min A Jhun; Lawrence F Bielak; Wei Zhao; Jennifer A Smith; Patricia A Peyser; Sharon L R Kardia; Glen A Satten
Journal:  Am J Hum Genet       Date:  2015-03-19       Impact factor: 11.025

4.  Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.

Authors:  Elizabeth J Leslie; Margaret A Taub; Huan Liu; Karyn Meltz Steinberg; Daniel C Koboldt; Qunyuan Zhang; Jenna C Carlson; Jacqueline B Hetmanski; Hang Wang; David E Larson; Robert S Fulton; Youssef A Kousa; Walid D Fakhouri; Ali Naji; Ingo Ruczinski; Ferdouse Begum; Margaret M Parker; Tamara Busch; Jennifer Standley; Jennifer Rigdon; Jacqueline T Hecht; Alan F Scott; George L Wehby; Kaare Christensen; Andrew E Czeizel; Frederic W-B Deleyiannis; Brian C Schutte; Richard K Wilson; Robert A Cornell; Andrew C Lidral; George M Weinstock; Terri H Beaty; Mary L Marazita; Jeffrey C Murray
Journal:  Am J Hum Genet       Date:  2015-02-19       Impact factor: 11.025

5.  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

6.  Sequence kernel association tests for the combined effect of rare and common variants.

Authors:  Iuliana Ionita-Laza; Seunggeun Lee; Vlad Makarov; Joseph D Buxbaum; Xihong Lin
Journal:  Am J Hum Genet       Date:  2013-05-16       Impact factor: 11.025

7.  The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.

Authors:  Zongxiao He; Di Zhang; Alan E Renton; Biao Li; Linhai Zhao; Gao T Wang; Alison M Goate; Richard Mayeux; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2017-01-05       Impact factor: 11.025

8.  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 9.  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

10.  Utilizing population controls in rare-variant case-parent association tests.

Authors:  Yu Jiang; Glen A Satten; Yujun Han; Michael P Epstein; Erin L Heinzen; David B Goldstein; Andrew S Allen
Journal:  Am J Hum Genet       Date:  2014-05-15       Impact factor: 11.025

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