Literature DB >> 23853078

Genotype imputation in genome-wide association studies.

Eleonora Porcu1, Serena Sanna, Christian Fuchsberger, Lars G Fritsche.   

Abstract

Imputation is an in silico method that can increase the power of association studies by inferring missing genotypes, harmonizing data sets for meta-analyses, and increasing the overall number of markers available for association testing. This unit provides an introductory overview of the imputation method and describes a two-step imputation approach that consists of the phasing of the study genotypes and the imputation of reference panel genotypes into the study haplotypes. Detailed steps for data preparation and quality control illustrate how to run the computationally intensive two-step imputation with the high-density reference panels of the 1000 Genomes Project, which currently integrates more than 39 million variants. Additionally, the influence of reference panel selection, input marker density, and imputation settings on imputation quality are demonstrated with a simulated data set to give insight into crucial points of successful genotype imputation. 2013 by John Wiley & Sons, Inc.

Mesh:

Year:  2013        PMID: 23853078     DOI: 10.1002/0471142905.hg0125s78

Source DB:  PubMed          Journal:  Curr Protoc Hum Genet        ISSN: 1934-8258


  15 in total

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Journal:  Int J Clin Exp Med       Date:  2015-10-15

2.  Genetic polymorphisms in CDH1 are associated with endometrial carcinoma susceptibility among Chinese Han women.

Authors:  Yue-Hang Geng; Zi-Fan Wang; Yu-Mian Jia; Li-Yuan Zheng; Lan Chen; Dong-Ge Liu; Xiang-Hong Li; Xin-Xia Tian; Wei-Gang Fang
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Review 3.  Inherited genetic variation in childhood acute lymphoblastic leukemia.

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Journal:  Blood       Date:  2015-05-21       Impact factor: 22.113

4.  Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.

Authors:  Giorgio Pistis; Eleonora Porcu; Scott I Vrieze; Carlo Sidore; Maristella Steri; Fabrice Danjou; Fabio Busonero; Antonella Mulas; Magdalena Zoledziewska; Andrea Maschio; Christine Brennan; Sandra Lai; Michael B Miller; Marco Marcelli; Maria Francesca Urru; Maristella Pitzalis; Robert H Lyons; Hyun M Kang; Chris M Jones; Andrea Angius; William G Iacono; David Schlessinger; Matt McGue; Francesco Cucca; Gonçalo R Abecasis; Serena Sanna
Journal:  Eur J Hum Genet       Date:  2014-10-08       Impact factor: 4.246

Review 5.  Using GWAS to identify novel therapeutic targets for osteoporosis.

Authors:  Olivia L Sabik; Charles R Farber
Journal:  Transl Res       Date:  2016-10-27       Impact factor: 7.012

6.  A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women.

Authors:  Hye-Young Yoo; Ki-Chan Lee; Ji-Eun Woo; Sung-Ha Park; Sunghoon Lee; Joungsu Joo; Jin-Sik Bae; Hyuk-Jung Kwon; Byoung-Jun Park
Journal:  Clin Cosmet Investig Dermatol       Date:  2022-03-11

7.  Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2.

Authors:  Lukas M Simon; Edward S Chen; Leonard C Edelstein; Xianguo Kong; Seema Bhatlekar; Isidore Rigoutsos; Paul F Bray; Chad A Shaw
Journal:  Am J Hum Genet       Date:  2016-04-28       Impact factor: 11.025

8.  Genome-Wide Association in Tomato Reveals 44 Candidate Loci for Fruit Metabolic Traits.

Authors:  Christopher Sauvage; Vincent Segura; Guillaume Bauchet; Rebecca Stevens; Phuc Thi Do; Zoran Nikoloski; Alisdair R Fernie; Mathilde Causse
Journal:  Plant Physiol       Date:  2014-06-03       Impact factor: 8.340

9.  Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.

Authors:  Momoko Horikoshi; Reedik Mӓgi; Martijn van de Bunt; Ida Surakka; Antti-Pekka Sarin; Anubha Mahajan; Letizia Marullo; Gudmar Thorleifsson; Sara Hӓgg; Jouke-Jan Hottenga; Claes Ladenvall; Janina S Ried; Thomas W Winkler; Sara M Willems; Natalia Pervjakova; Tõnu Esko; Marian Beekman; Christopher P Nelson; Christina Willenborg; Steven Wiltshire; Teresa Ferreira; Juan Fernandez; Kyle J Gaulton; Valgerdur Steinthorsdottir; Anders Hamsten; Patrik K E Magnusson; Gonneke Willemsen; Yuri Milaneschi; Neil R Robertson; Christopher J Groves; Amanda J Bennett; Terho Lehtimӓki; Jorma S Viikari; Johan Rung; Valeriya Lyssenko; Markus Perola; Iris M Heid; Christian Herder; Harald Grallert; Martina Müller-Nurasyid; Michael Roden; Elina Hypponen; Aaron Isaacs; Elisabeth M van Leeuwen; Lennart C Karssen; Evelin Mihailov; Jeanine J Houwing-Duistermaat; Anton J M de Craen; Joris Deelen; Aki S Havulinna; Matthew Blades; Christian Hengstenberg; Jeanette Erdmann; Heribert Schunkert; Jaakko Kaprio; Martin D Tobin; Nilesh J Samani; Lars Lind; Veikko Salomaa; Cecilia M Lindgren; P Eline Slagboom; Andres Metspalu; Cornelia M van Duijn; Johan G Eriksson; Annette Peters; Christian Gieger; Antti Jula; Leif Groop; Olli T Raitakari; Chris Power; Brenda W J H Penninx; Eco de Geus; Johannes H Smit; Dorret I Boomsma; Nancy L Pedersen; Erik Ingelsson; Unnur Thorsteinsdottir; Kari Stefansson; Samuli Ripatti; Inga Prokopenko; Mark I McCarthy; Andrew P Morris
Journal:  PLoS Genet       Date:  2015-07-01       Impact factor: 5.917

Review 10.  Computational studies of DNA sequencing with solid-state nanopores: key issues and future prospects.

Authors:  Lijun Liang; Qi Wang; Hans Agren; Yaoquan Tu
Journal:  Front Chem       Date:  2014-02-21       Impact factor: 5.221

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