Literature DB >> 30918937

Kinpute: using identity by descent to improve genotype imputation.

Mark Abney1, Aisha ElSherbiny1.   

Abstract

MOTIVATION: Genotype imputation, though generally accurate, often results in many genotypes being poorly imputed, particularly in studies where the individuals are not well represented by standard reference panels. When individuals in the study share regions of the genome identical by descent (IBD), it is possible to use this information in combination with a study-specific reference panel (SSRP) to improve the imputation results. Kinpute uses IBD information-due to recent, familial relatedness or distant, unknown ancestors-in conjunction with the output from linkage disequilibrium (LD) based imputation methods to compute more accurate genotype probabilities. Kinpute uses a novel method for IBD imputation, which works even in the absence of a pedigree, and results in substantially improved imputation quality.
RESULTS: Given initial estimates of average IBD between subjects in the study sample, Kinpute uses a novel algorithm to select an optimal set of individuals to sequence and use as an SSRP. Kinpute is designed to use as input both this SSRP and the genotype probabilities output from other LD-based imputation software, and uses a new method to combine the LD imputed genotype probabilities with IBD configurations to substantially improve imputation. We tested Kinpute on a human population isolate where 98 individuals have been sequenced. In half of this sample, whose sequence data was masked, we used Impute2 to perform LD-based imputation and Kinpute was used to obtain higher accuracy genotype probabilities. Measures of imputation accuracy improved significantly, particularly for those genotypes that Impute2 imputed with low certainty.
AVAILABILITY AND IMPLEMENTATION: Kinpute is an open-source and freely available C++ software package that can be downloaded from. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Year:  2019        PMID: 30918937      PMCID: PMC6821425          DOI: 10.1093/bioinformatics/btz221

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


  29 in total

1.  In silico method for inferring genotypes in pedigrees.

Authors:  Joshua T Burdick; Wei-Min Chen; Gonçalo R Abecasis; Vivian G Cheung
Journal:  Nat Genet       Date:  2006-08-20       Impact factor: 38.330

2.  A One-Penny Imputed Genome from Next-Generation Reference Panels.

Authors:  Brian L Browning; Ying Zhou; Sharon R Browning
Journal:  Am J Hum Genet       Date:  2018-08-09       Impact factor: 11.025

3.  Strategies for phasing and imputation in a population isolate.

Authors:  Anthony Francis Herzig; Teresa Nutile; Marie-Claude Babron; Marina Ciullo; Céline Bellenguez; Anne-Louise Leutenegger
Journal:  Genet Epidemiol       Date:  2018-01-10       Impact factor: 2.135

4.  Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees.

Authors:  Mohamad Saad; Ellen M Wijsman
Journal:  Genet Epidemiol       Date:  2014-08-01       Impact factor: 2.135

5.  Detection of sharing by descent, long-range phasing and haplotype imputation.

Authors:  Augustine Kong; Gisli Masson; Michael L Frigge; Arnaldur Gylfason; Pasha Zusmanovich; Gudmar Thorleifsson; Pall I Olason; Andres Ingason; Stacy Steinberg; Thorunn Rafnar; Patrick Sulem; Magali Mouy; Frosti Jonsson; Unnur Thorsteinsdottir; Daniel F Gudbjartsson; Hreinn Stefansson; Kari Stefansson
Journal:  Nat Genet       Date:  2008-09       Impact factor: 38.330

6.  Fast and accurate genotype imputation in genome-wide association studies through pre-phasing.

Authors:  Bryan Howie; Christian Fuchsberger; Matthew Stephens; Jonathan Marchini; Gonçalo R Abecasis
Journal:  Nat Genet       Date:  2012-07-22       Impact factor: 38.330

7.  Identity-by-descent-based phasing and imputation in founder populations using graphical models.

Authors:  Kimmo Palin; Harry Campbell; Alan F Wright; James F Wilson; Richard Durbin
Journal:  Genet Epidemiol       Date:  2011-10-17       Impact factor: 2.135

8.  PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.

Authors:  Oren E Livne; Lide Han; Gorka Alkorta-Aranburu; William Wentworth-Sheilds; Mark Abney; Carole Ober; Dan L Nicolae
Journal:  PLoS Comput Biol       Date:  2015-03-03       Impact factor: 4.475

9.  A reference panel of 64,976 haplotypes for genotype imputation.

Authors:  Shane McCarthy; Sayantan Das; Warren Kretzschmar; Olivier Delaneau; Andrew R Wood; Alexander Teumer; Hyun Min Kang; Christian Fuchsberger; Petr Danecek; Kevin Sharp; Yang Luo; Carlo Sidore; Alan Kwong; Nicholas Timpson; Seppo Koskinen; Scott Vrieze; Laura J Scott; He Zhang; Anubha Mahajan; Jan Veldink; Ulrike Peters; Carlos Pato; Cornelia M van Duijn; Christopher E Gillies; Ilaria Gandin; Massimo Mezzavilla; Arthur Gilly; Massimiliano Cocca; Michela Traglia; Andrea Angius; Jeffrey C Barrett; Dorrett Boomsma; Kari Branham; Gerome Breen; Chad M Brummett; Fabio Busonero; Harry Campbell; Andrew Chan; Sai Chen; Emily Chew; Francis S Collins; Laura J Corbin; George Davey Smith; George Dedoussis; Marcus Dorr; Aliki-Eleni Farmaki; Luigi Ferrucci; Lukas Forer; Ross M Fraser; Stacey Gabriel; Shawn Levy; Leif Groop; Tabitha Harrison; Andrew Hattersley; Oddgeir L Holmen; Kristian Hveem; Matthias Kretzler; James C Lee; Matt McGue; Thomas Meitinger; David Melzer; Josine L Min; Karen L Mohlke; John B Vincent; Matthias Nauck; Deborah Nickerson; Aarno Palotie; Michele Pato; Nicola Pirastu; Melvin McInnis; J Brent Richards; Cinzia Sala; Veikko Salomaa; David Schlessinger; Sebastian Schoenherr; P Eline Slagboom; Kerrin Small; Timothy Spector; Dwight Stambolian; Marcus Tuke; Jaakko Tuomilehto; Leonard H Van den Berg; Wouter Van Rheenen; Uwe Volker; Cisca Wijmenga; Daniela Toniolo; Eleftheria Zeggini; Paolo Gasparini; Matthew G Sampson; James F Wilson; Timothy Frayling; Paul I W de Bakker; Morris A Swertz; Steven McCarroll; Charles Kooperberg; Annelot Dekker; David Altshuler; Cristen Willer; William Iacono; Samuli Ripatti; Nicole Soranzo; Klaudia Walter; Anand Swaroop; Francesco Cucca; Carl A Anderson; Richard M Myers; Michael Boehnke; Mark I McCarthy; Richard Durbin
Journal:  Nat Genet       Date:  2016-08-22       Impact factor: 38.330

10.  A population-specific reference panel empowers genetic studies of Anabaptist populations.

Authors:  Liping Hou; Rachel L Kember; Jared C Roach; Jeffrey R O'Connell; David W Craig; Maja Bucan; William K Scott; Margaret Pericak-Vance; Jonathan L Haines; Michael H Crawford; Alan R Shuldiner; Francis J McMahon
Journal:  Sci Rep       Date:  2017-07-20       Impact factor: 4.379

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