Literature DB >> 20940738

Statistical analysis strategies for association studies involving rare variants.

Vikas Bansal1, Ondrej Libiger, Ali Torkamani, Nicholas J Schork.   

Abstract

The limitations of genome-wide association (GWA) studies that focus on the phenotypic influence of common genetic variants have motivated human geneticists to consider the contribution of rare variants to phenotypic expression. The increasing availability of high-throughput sequencing technologies has enabled studies of rare variants but these methods will not be sufficient for their success as appropriate analytical methods are also needed. We consider data analysis approaches to testing associations between a phenotype and collections of rare variants in a defined genomic region or set of regions. Ultimately, although a wide variety of analytical approaches exist, more work is needed to refine them and determine their properties and power in different contexts.

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Year:  2010        PMID: 20940738      PMCID: PMC3743540          DOI: 10.1038/nrg2867

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  133 in total

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

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2.  Interpretation of association signals and identification of causal variants from genome-wide association studies.

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3.  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

Review 4.  Rare variant association analysis methods for complex traits.

Authors:  Jennifer Asimit; Eleftheria Zeggini
Journal:  Annu Rev Genet       Date:  2010       Impact factor: 16.830

5.  An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype.

Authors:  Vikas Bansal; Ondrej Libiger; Ali Torkamani; Nicholas J Schork
Journal:  Pac Symp Biocomput       Date:  2011

6.  Analysis of genetic inheritance in a family quartet by whole-genome sequencing.

Authors:  Jared C Roach; Gustavo Glusman; Arian F A Smit; Chad D Huff; Robert Hubley; Paul T Shannon; Lee Rowen; Krishna P Pant; Nathan Goodman; Michael Bamshad; Jay Shendure; Radoje Drmanac; Lynn B Jorde; Leroy Hood; David J Galas
Journal:  Science       Date:  2010-03-10       Impact factor: 47.728

7.  Hierarchical modeling for estimating relative risks of rare genetic variants: properties of the pseudo-likelihood method.

Authors:  Marinela Capanu; Colin B Begg
Journal:  Biometrics       Date:  2010-08-05       Impact factor: 2.571

8.  Common genetic variation and performance on standardized cognitive tests.

Authors:  Elizabeth T Cirulli; Dalia Kasperaviciūte; Deborah K Attix; Anna C Need; Dongliang Ge; Greg Gibson; David B Goldstein
Journal:  Eur J Hum Genet       Date:  2010-02-03       Impact factor: 4.246

9.  Association tests using kernel-based measures of multi-locus genotype similarity between individuals.

Authors:  Indranil Mukhopadhyay; Eleanor Feingold; Daniel E Weeks; Anbupalam Thalamuthu
Journal:  Genet Epidemiol       Date:  2010-04       Impact factor: 2.135

10.  Functional impact of global rare copy number variation in autism spectrum disorders.

Authors:  Dalila Pinto; Alistair T Pagnamenta; Lambertus Klei; Richard Anney; Daniele Merico; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S Abrahams; Joana Almeida; Elena Bacchelli; Gary D Bader; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Susan E Bryson; Andrew R Carson; Guillermo Casallo; Jillian Casey; Brian H Y Chung; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Cheryl Cytrynbaum; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Andrew Green; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao-Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Marion Pilorge; Joseph Piven; Chris P Ponting; David J Posey; Annemarie Poustka; Fritz Poustka; Aparna Prasad; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Ana F Sequeira; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Olaf Stein; Nuala Sykes; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Wang; Thomas H Wassink; Caleb Webber; Rosanna Weksberg; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Jing Wu; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Bernie Devlin; Sean Ennis; Louise Gallagher; Daniel H Geschwind; Michael Gill; Jonathan L Haines; Joachim Hallmayer; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret A Pericak-Vance; Gerard D Schellenberg; Peter Szatmari; Astrid M Vicente; Veronica J Vieland; Ellen M Wijsman; Stephen W Scherer; James S Sutcliffe; Catalina Betancur
Journal:  Nature       Date:  2010-06-09       Impact factor: 49.962

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  260 in total

1.  Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition.

Authors:  Laura B Ramsey; Gitte H Bruun; Wenjian Yang; Lisa R Treviño; Selina Vattathil; Paul Scheet; Cheng Cheng; Gary L Rosner; Kathleen M Giacomini; Yiping Fan; Alex Sparreboom; Torben S Mikkelsen; Thomas J Corydon; Ching-Hon Pui; William E Evans; Mary V Relling
Journal:  Genome Res       Date:  2011-12-06       Impact factor: 9.043

2.  Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.

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Journal:  Genet Epidemiol       Date:  2011-12-06       Impact factor: 2.135

Review 3.  Unraveling the genetic component of systemic sclerosis.

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Journal:  Hum Genet       Date:  2012-01-05       Impact factor: 4.132

4.  Properties and power of the Drosophila Synthetic Population Resource for the routine dissection of complex traits.

Authors:  Elizabeth G King; Stuart J Macdonald; Anthony D Long
Journal:  Genetics       Date:  2012-04-13       Impact factor: 4.562

5.  Mapping rare and common causal alleles for complex human diseases.

Authors:  Soumya Raychaudhuri
Journal:  Cell       Date:  2011-09-30       Impact factor: 41.582

6.  Assessing the impact of non-differential genotyping errors on rare variant tests of association.

Authors:  Scott Powers; Shyam Gopalakrishnan; Nathan Tintle
Journal:  Hum Hered       Date:  2011-10-15       Impact factor: 0.444

7.  Exome sequencing and the genetic basis of complex traits.

Authors:  Adam Kiezun; Kiran Garimella; Ron Do; Nathan O Stitziel; Benjamin M Neale; Paul J McLaren; Namrata Gupta; Pamela Sklar; Patrick F Sullivan; Jennifer L Moran; Christina M Hultman; Paul Lichtenstein; Patrik Magnusson; Thomas Lehner; Yin Yao Shugart; Alkes L Price; Paul I W de Bakker; Shaun M Purcell; Shamil R Sunyaev
Journal:  Nat Genet       Date:  2012-05-29       Impact factor: 38.330

8.  Family-based association studies for next-generation sequencing.

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Journal:  Am J Hum Genet       Date:  2012-06-08       Impact factor: 11.025

9.  A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data.

Authors:  Li Luo; Yun Zhu; Momiao Xiong
Journal:  J Comput Biol       Date:  2012-05-31       Impact factor: 1.479

10.  Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects.

Authors:  Caroline M Nievergelt; Nathan E Wineinger; Ondrej Libiger; Phillip Pham; Guangfa Zhang; Dewleen G Baker; Nicholas J Schork
Journal:  Gene       Date:  2014-02-09       Impact factor: 3.688

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