Literature DB >> 23361219

Inference of identity by descent in population isolates and optimal sequencing studies.

Dominik Glodzik1, Pau Navarro, Veronique Vitart, Caroline Hayward, Ruth McQuillan, Sarah H Wild, Malcolm G Dunlop, Igor Rudan, Harry Campbell, Chris Haley, Alan F Wright, James F Wilson, Paul McKeigue.   

Abstract

In an isolated population, individuals are likely to share large genetic regions inherited from common ancestors. Identity by descent (IBD) can be inferred from SNP genotypes, which is useful in a number of applications, including identifying genetic variants influencing complex disease risk, and planning efficient cohort-sequencing strategies. We present ANCHAP--a method for detecting IBD in isolated populations. We compare accuracy of the method against other long-range and local phasing methods, using parent-offspring trios. In our experiments, we show that ANCHAP performs similarly as the other long-range method, but requires an order-of-magnitude less computational resources. A local phasing model is able to achieve similar sensitivity, but only at the cost of higher false discovery rates. In some regions of the genome, the studied individuals share haplotypes particularly often, which hints at the history of the populations studied. We demonstrate the method using SNP genotypes from three isolated island populations, as well as in a cohort of unrelated individuals. In samples from three isolated populations of around 1000 individual each, an average individual shares a haplotype at a genetic locus with 9-12 other individuals, compared with only 1 individual within the non-isolated population. We describe an application of ANCHAP to optimally choose samples in resequencing studies. We find that with sample sizes of 1000 individuals from an isolated population genotyped using a dense SNP array, and with 20% of these individuals sequenced, 65% of sequences of the unsequenced subjects can be partially inferred.

Mesh:

Year:  2013        PMID: 23361219      PMCID: PMC3778345          DOI: 10.1038/ejhg.2012.307

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


  25 in total

1.  High-resolution detection of identity by descent in unrelated individuals.

Authors:  Sharon R Browning; Brian L Browning
Journal:  Am J Hum Genet       Date:  2010-03-18       Impact factor: 11.025

2.  A fine-scale map of recombination rates and hotspots across the human genome.

Authors:  Simon Myers; Leonardo Bottolo; Colin Freeman; Gil McVean; Peter Donnelly
Journal:  Science       Date:  2005-10-14       Impact factor: 47.728

3.  Runs of homozygosity in European populations.

Authors:  Ruth McQuillan; Anne-Louise Leutenegger; Rehab Abdel-Rahman; Christopher S Franklin; Marijana Pericic; Lovorka Barac-Lauc; Nina Smolej-Narancic; Branka Janicijevic; Ozren Polasek; Albert Tenesa; Andrew K Macleod; Susan M Farrington; Pavao Rudan; Caroline Hayward; Veronique Vitart; Igor Rudan; Sarah H Wild; Malcolm G Dunlop; Alan F Wright; Harry Campbell; James F Wilson
Journal:  Am J Hum Genet       Date:  2008-08-28       Impact factor: 11.025

Review 4.  Linkage disequilibrium mapping of complex disease: fantasy or reality?

Authors:  J D Terwilliger; K M Weiss
Journal:  Curr Opin Biotechnol       Date:  1998-12       Impact factor: 9.740

5.  Improved IBD detection using incomplete haplotype information.

Authors:  Giulio Genovese; Gregory Leibon; Martin R Pollak; Daniel N Rockmore
Journal:  BMC Genet       Date:  2010-06-30       Impact factor: 2.797

6.  Genome-wide association study of anthropometric traits in Korcula Island, Croatia.

Authors:  Ozren Polasek; Ana Marusić; Kresimir Rotim; Caroline Hayward; Veronique Vitart; Jennifer Huffman; Susan Campbell; Stipan Janković; Mladen Boban; Zrinka Biloglav; Ivana Kolcić; Vjekoslav Krzelj; Janos Terzić; Lana Matec; Gordan Tometić; Dijana Nonković; Jasna Nincević; Marina Pehlić; Jurica Zedelj; Vedran Velagić; Danica Juricić; Iva Kirac; Sanja Belak Kovacević; Alan F Wright; Harry Campbell; Igor Rudan
Journal:  Croat Med J       Date:  2009-02       Impact factor: 1.351

7.  A second generation human haplotype map of over 3.1 million SNPs.

Authors:  Kelly A Frazer; Dennis G Ballinger; David R Cox; David A Hinds; Laura L Stuve; Richard A Gibbs; John W Belmont; Andrew Boudreau; Paul Hardenbol; Suzanne M Leal; Shiran Pasternak; David A Wheeler; Thomas D Willis; Fuli Yu; Huanming Yang; Changqing Zeng; Yang Gao; Haoran Hu; Weitao Hu; Chaohua Li; Wei Lin; Siqi Liu; Hao Pan; Xiaoli Tang; Jian Wang; Wei Wang; Jun Yu; Bo Zhang; Qingrun Zhang; Hongbin Zhao; Hui Zhao; Jun Zhou; Stacey B Gabriel; Rachel Barry; Brendan Blumenstiel; Amy Camargo; Matthew Defelice; Maura Faggart; Mary Goyette; Supriya Gupta; Jamie Moore; Huy Nguyen; Robert C Onofrio; Melissa Parkin; Jessica Roy; Erich Stahl; Ellen Winchester; Liuda Ziaugra; David Altshuler; Yan Shen; Zhijian Yao; Wei Huang; Xun Chu; Yungang He; Li Jin; Yangfan Liu; Yayun Shen; Weiwei Sun; Haifeng Wang; Yi Wang; Ying Wang; Xiaoyan Xiong; Liang Xu; Mary M Y Waye; Stephen K W Tsui; Hong Xue; J Tze-Fei Wong; Luana M Galver; Jian-Bing Fan; Kevin Gunderson; Sarah S Murray; Arnold R Oliphant; Mark S Chee; Alexandre Montpetit; Fanny Chagnon; Vincent Ferretti; Martin Leboeuf; Jean-François Olivier; Michael S Phillips; Stéphanie Roumy; Clémentine Sallée; Andrei Verner; Thomas J Hudson; Pui-Yan Kwok; Dongmei Cai; Daniel C Koboldt; Raymond D Miller; Ludmila Pawlikowska; Patricia Taillon-Miller; Ming Xiao; Lap-Chee Tsui; William Mak; You Qiang Song; Paul K H Tam; Yusuke Nakamura; Takahisa Kawaguchi; Takuya Kitamoto; Takashi Morizono; Atsushi Nagashima; Yozo Ohnishi; Akihiro Sekine; Toshihiro Tanaka; Tatsuhiko Tsunoda; Panos Deloukas; Christine P Bird; Marcos Delgado; Emmanouil T Dermitzakis; Rhian Gwilliam; Sarah Hunt; Jonathan Morrison; Don Powell; Barbara E Stranger; Pamela Whittaker; David R Bentley; Mark J Daly; Paul I W de Bakker; Jeff Barrett; Yves R Chretien; Julian Maller; Steve McCarroll; Nick Patterson; Itsik Pe'er; Alkes Price; Shaun Purcell; Daniel J Richter; Pardis Sabeti; Richa Saxena; Stephen F Schaffner; Pak C Sham; Patrick Varilly; David Altshuler; Lincoln D Stein; Lalitha Krishnan; Albert Vernon Smith; Marcela K Tello-Ruiz; Gudmundur A Thorisson; Aravinda Chakravarti; Peter E Chen; David J Cutler; Carl S Kashuk; Shin Lin; Gonçalo R Abecasis; Weihua Guan; Yun Li; Heather M Munro; Zhaohui Steve Qin; Daryl J Thomas; Gilean McVean; Adam Auton; Leonardo Bottolo; Niall Cardin; Susana Eyheramendy; Colin Freeman; Jonathan Marchini; Simon Myers; Chris Spencer; Matthew Stephens; Peter Donnelly; Lon R Cardon; Geraldine Clarke; David M Evans; Andrew P Morris; Bruce S Weir; Tatsuhiko Tsunoda; James C Mullikin; Stephen T Sherry; Michael Feolo; Andrew Skol; Houcan Zhang; Changqing Zeng; Hui Zhao; Ichiro Matsuda; Yoshimitsu Fukushima; Darryl R Macer; Eiko Suda; Charles N Rotimi; Clement A Adebamowo; Ike Ajayi; Toyin Aniagwu; Patricia A Marshall; Chibuzor Nkwodimmah; Charmaine D M Royal; Mark F Leppert; Missy Dixon; Andy Peiffer; Renzong Qiu; Alastair Kent; Kazuto Kato; Norio Niikawa; Isaac F Adewole; Bartha M Knoppers; Morris W Foster; Ellen Wright Clayton; Jessica Watkin; Richard A Gibbs; John W Belmont; Donna Muzny; Lynne Nazareth; Erica Sodergren; George M Weinstock; David A Wheeler; Imtaz Yakub; Stacey B Gabriel; Robert C Onofrio; Daniel J Richter; Liuda Ziaugra; Bruce W Birren; Mark J Daly; David Altshuler; Richard K Wilson; Lucinda L Fulton; Jane Rogers; John Burton; Nigel P Carter; Christopher M Clee; Mark Griffiths; Matthew C Jones; Kirsten McLay; Robert W Plumb; Mark T Ross; Sarah K Sims; David L Willey; Zhu Chen; Hua Han; Le Kang; Martin Godbout; John C Wallenburg; Paul L'Archevêque; Guy Bellemare; Koji Saeki; Hongguang Wang; Daochang An; Hongbo Fu; Qing Li; Zhen Wang; Renwu Wang; Arthur L Holden; Lisa D Brooks; Jean E McEwen; Mark S Guyer; Vivian Ota Wang; Jane L Peterson; Michael Shi; Jack Spiegel; Lawrence M Sung; Lynn F Zacharia; Francis S Collins; Karen Kennedy; Ruth Jamieson; John Stewart
Journal:  Nature       Date:  2007-10-18       Impact factor: 49.962

8.  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

9.  Parental origin of sequence variants associated with complex diseases.

Authors:  Augustine Kong; Valgerdur Steinthorsdottir; Gisli Masson; Gudmar Thorleifsson; Patrick Sulem; Soren Besenbacher; Aslaug Jonasdottir; Asgeir Sigurdsson; Kari Th Kristinsson; Adalbjorg Jonasdottir; Michael L Frigge; Arnaldur Gylfason; Pall I Olason; Sigurjon A Gudjonsson; Sverrir Sverrisson; Simon N Stacey; Bardur Sigurgeirsson; Kristrun R Benediktsdottir; Helgi Sigurdsson; Thorvaldur Jonsson; Rafn Benediktsson; Jon H Olafsson; Oskar Th Johannsson; Astradur B Hreidarsson; Gunnar Sigurdsson; Anne C Ferguson-Smith; Daniel F Gudbjartsson; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nature       Date:  2009-12-17       Impact factor: 49.962

10.  Mutation patterns in the human genome: more variable than expected.

Authors:  Laurent Duret
Journal:  PLoS Biol       Date:  2009-02-03       Impact factor: 8.029

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  11 in total

1.  Extensive genome-wide autozygosity in the population isolates of Daghestan.

Authors:  Tatiana M Karafet; Kazima B Bulayeva; Oleg A Bulayev; Farida Gurgenova; Jamilia Omarova; Levon Yepiskoposyan; Olga V Savina; Krishna R Veeramah; Michael F Hammer
Journal:  Eur J Hum Genet       Date:  2015-01-21       Impact factor: 4.246

2.  Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.

Authors:  Alicia R Martin; Konrad J Karczewski; Sini Kerminen; Mitja I Kurki; Antti-Pekka Sarin; Mykyta Artomov; Johan G Eriksson; Tõnu Esko; Giulio Genovese; Aki S Havulinna; Jaakko Kaprio; Alexandra Konradi; László Korányi; Anna Kostareva; Minna Männikkö; Andres Metspalu; Markus Perola; Rashmi B Prasad; Olli Raitakari; Oxana Rotar; Veikko Salomaa; Leif Groop; Aarno Palotie; Benjamin M Neale; Samuli Ripatti; Matti Pirinen; Mark J Daly
Journal:  Am J Hum Genet       Date:  2018-04-26       Impact factor: 11.025

Review 3.  Efficient genome-wide genotyping strategies and data integration in crop plants.

Authors:  Davoud Torkamaneh; Brian Boyle; François Belzile
Journal:  Theor Appl Genet       Date:  2018-01-19       Impact factor: 5.699

4.  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

5.  Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.

Authors:  Stefan Enroth; Asa Johansson; Sofia Bosdotter Enroth; Ulf Gyllensten
Journal:  Nat Commun       Date:  2014-08-22       Impact factor: 14.919

6.  Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.

Authors:  Peter K Joshi; James Prendergast; Ross M Fraser; Jennifer E Huffman; Veronique Vitart; Caroline Hayward; Ruth McQuillan; Dominik Glodzik; Ozren Polašek; Nicholas D Hastie; Igor Rudan; Harry Campbell; Alan F Wright; Chris S Haley; James F Wilson; Pau Navarro
Journal:  PLoS One       Date:  2013-07-16       Impact factor: 3.240

7.  A general approach for haplotype phasing across the full spectrum of relatedness.

Authors:  Jared O'Connell; Deepti Gurdasani; Olivier Delaneau; Nicola Pirastu; Sheila Ulivi; Massimiliano Cocca; Michela Traglia; Jie Huang; Jennifer E Huffman; Igor Rudan; Ruth McQuillan; Ross M Fraser; Harry Campbell; Ozren Polasek; Gershim Asiki; Kenneth Ekoru; Caroline Hayward; Alan F Wright; Veronique Vitart; Pau Navarro; Jean-Francois Zagury; James F Wilson; Daniela Toniolo; Paolo Gasparini; Nicole Soranzo; Manjinder S Sandhu; Jonathan Marchini
Journal:  PLoS Genet       Date:  2014-04-17       Impact factor: 5.917

Review 8.  Using population isolates in genetic association studies.

Authors:  Konstantinos Hatzikotoulas; Arthur Gilly; Eleftheria Zeggini
Journal:  Brief Funct Genomics       Date:  2014-07-09       Impact factor: 4.241

9.  Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.

Authors:  Ana Jeroncic; Yasin Memari; Graham Rs Ritchie; Audrey E Hendricks; Anja Kolb-Kokocinski; Angela Matchan; Veronique Vitart; Caroline Hayward; Ivana Kolcic; Dominik Glodzik; Alan F Wright; Igor Rudan; Harry Campbell; Richard Durbin; Ozren Polašek; Eleftheria Zeggini; Vesna Boraska Perica
Journal:  Eur J Hum Genet       Date:  2016-04-06       Impact factor: 4.246

10.  An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.

Authors:  Shona M Kerr; Lucija Klaric; Mihail Halachev; Caroline Hayward; Thibaud S Boutin; Alison M Meynert; Colin A Semple; Annukka M Tuiskula; Heikki Swan; Javier Santoyo-Lopez; Veronique Vitart; Chris Haley; John Dean; Zosia Miedzybrodzka; Timothy J Aitman; James F Wilson
Journal:  Sci Rep       Date:  2019-07-29       Impact factor: 4.379

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