Literature DB >> 26249230

Global diversity, population stratification, and selection of human copy-number variation.

Peter H Sudmant1, Swapan Mallick2, Bradley J Nelson1, Fereydoun Hormozdiari1, Niklas Krumm1, John Huddleston3, Bradley P Coe1, Carl Baker1, Susanne Nordenfelt2, Michael Bamshad4, Lynn B Jorde5, Olga L Posukh6, Hovhannes Sahakyan7, W Scott Watkins8, Levon Yepiskoposyan9, M Syafiq Abdullah10, Claudio M Bravi11, Cristian Capelli12, Tor Hervig13, Joseph T S Wee14, Chris Tyler-Smith15, George van Driem16, Irene Gallego Romero17, Aashish R Jha17, Sena Karachanak-Yankova18, Draga Toncheva18, David Comas19, Brenna Henn20, Toomas Kivisild21, Andres Ruiz-Linares22, Antti Sajantila23, Ene Metspalu24, Jüri Parik25, Richard Villems25, Elena B Starikovskaya26, George Ayodo27, Cynthia M Beall28, Anna Di Rienzo17, Michael F Hammer29, Rita Khusainova30, Elza Khusnutdinova30, William Klitz31, Cheryl Winkler32, Damian Labuda33, Mait Metspalu25, Sarah A Tishkoff34, Stanislav Dryomov35, Rem Sukernik36, Nick Patterson2, David Reich37, Evan E Eichler38.   

Abstract

In order to explore the diversity and selective signatures of duplication and deletion human copy-number variants (CNVs), we sequenced 236 individuals from 125 distinct human populations. We observed that duplications exhibit fundamentally different population genetic and selective signatures than deletions and are more likely to be stratified between human populations. Through reconstruction of the ancestral human genome, we identify megabases of DNA lost in different human lineages and pinpoint large duplications that introgressed from the extinct Denisova lineage now found at high frequency exclusively in Oceanic populations. We find that the proportion of CNV base pairs to single-nucleotide-variant base pairs is greater among non-Africans than it is among African populations, but we conclude that this difference is likely due to unique aspects of non-African population history as opposed to differences in CNV load.
Copyright © 2015, American Association for the Advancement of Science.

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Year:  2015        PMID: 26249230      PMCID: PMC4568308          DOI: 10.1126/science.aab3761

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  56 in total

1.  The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome.

Authors:  J E Horvath; S Schwartz; E E Eichler
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

2.  Genetic structure of human populations.

Authors:  Noah A Rosenberg; Jonathan K Pritchard; James L Weber; Howard M Cann; Kenneth K Kidd; Lev A Zhivotovsky; Marcus W Feldman
Journal:  Science       Date:  2002-12-20       Impact factor: 47.728

3.  Characteristics of neutral and deleterious protein-coding variation among individuals and populations.

Authors:  Wenqing Fu; Rachel M Gittelman; Michael J Bamshad; Joshua M Akey
Journal:  Am J Hum Genet       Date:  2014-10-02       Impact factor: 11.025

4.  Genome sequence of a 45,000-year-old modern human from western Siberia.

Authors:  Qiaomei Fu; Heng Li; Priya Moorjani; Flora Jay; Sergey M Slepchenko; Aleksei A Bondarev; Philip L F Johnson; Ayinuer Aximu-Petri; Kay Prüfer; Cesare de Filippo; Matthias Meyer; Nicolas Zwyns; Domingo C Salazar-García; Yaroslav V Kuzmin; Susan G Keates; Pavel A Kosintsev; Dmitry I Razhev; Michael P Richards; Nikolai V Peristov; Michael Lachmann; Katerina Douka; Thomas F G Higham; Montgomery Slatkin; Jean-Jacques Hublin; David Reich; Janet Kelso; T Bence Viola; Svante Pääbo
Journal:  Nature       Date:  2014-10-23       Impact factor: 49.962

5.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

6.  Constant darkness is a circadian metabolic signal in mammals.

Authors:  Jianfa Zhang; Krista Kaasik; Michael R Blackburn; Cheng Chi Lee
Journal:  Nature       Date:  2006-01-19       Impact factor: 49.962

7.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

8.  Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence.

Authors:  Joseph Cheung; Xavier Estivill; Razi Khaja; Jeffrey R MacDonald; Ken Lau; Lap-Chee Tsui; Stephen W Scherer
Journal:  Genome Biol       Date:  2003-03-17       Impact factor: 13.583

9.  Ancient human genomes suggest three ancestral populations for present-day Europeans.

Authors:  Iosif Lazaridis; Nick Patterson; Alissa Mittnik; Gabriel Renaud; Swapan Mallick; Karola Kirsanow; Peter H Sudmant; Joshua G Schraiber; Sergi Castellano; Mark Lipson; Bonnie Berger; Christos Economou; Ruth Bollongino; Qiaomei Fu; Kirsten I Bos; Susanne Nordenfelt; Heng Li; Cesare de Filippo; Kay Prüfer; Susanna Sawyer; Cosimo Posth; Wolfgang Haak; Fredrik Hallgren; Elin Fornander; Nadin Rohland; Dominique Delsate; Michael Francken; Jean-Michel Guinet; Joachim Wahl; George Ayodo; Hamza A Babiker; Graciela Bailliet; Elena Balanovska; Oleg Balanovsky; Ramiro Barrantes; Gabriel Bedoya; Haim Ben-Ami; Judit Bene; Fouad Berrada; Claudio M Bravi; Francesca Brisighelli; George B J Busby; Francesco Cali; Mikhail Churnosov; David E C Cole; Daniel Corach; Larissa Damba; George van Driem; Stanislav Dryomov; Jean-Michel Dugoujon; Sardana A Fedorova; Irene Gallego Romero; Marina Gubina; Michael Hammer; Brenna M Henn; Tor Hervig; Ugur Hodoglugil; Aashish R Jha; Sena Karachanak-Yankova; Rita Khusainova; Elza Khusnutdinova; Rick Kittles; Toomas Kivisild; William Klitz; Vaidutis Kučinskas; Alena Kushniarevich; Leila Laredj; Sergey Litvinov; Theologos Loukidis; Robert W Mahley; Béla Melegh; Ene Metspalu; Julio Molina; Joanna Mountain; Klemetti Näkkäläjärvi; Desislava Nesheva; Thomas Nyambo; Ludmila Osipova; Jüri Parik; Fedor Platonov; Olga Posukh; Valentino Romano; Francisco Rothhammer; Igor Rudan; Ruslan Ruizbakiev; Hovhannes Sahakyan; Antti Sajantila; Antonio Salas; Elena B Starikovskaya; Ayele Tarekegn; Draga Toncheva; Shahlo Turdikulova; Ingrida Uktveryte; Olga Utevska; René Vasquez; Mercedes Villena; Mikhail Voevoda; Cheryl A Winkler; Levon Yepiskoposyan; Pierre Zalloua; Tatijana Zemunik; Alan Cooper; Cristian Capelli; Mark G Thomas; Andres Ruiz-Linares; Sarah A Tishkoff; Lalji Singh; Kumarasamy Thangaraj; Richard Villems; David Comas; Rem Sukernik; Mait Metspalu; Matthias Meyer; Evan E Eichler; Joachim Burger; Montgomery Slatkin; Svante Pääbo; Janet Kelso; David Reich; Johannes Krause
Journal:  Nature       Date:  2014-09-18       Impact factor: 49.962

10.  Refining analyses of copy number variation identifies specific genes associated with developmental delay.

Authors:  Bradley P Coe; Kali Witherspoon; Jill A Rosenfeld; Bregje W M van Bon; Anneke T Vulto-van Silfhout; Paolo Bosco; Kathryn L Friend; Carl Baker; Serafino Buono; Lisenka E L M Vissers; Janneke H Schuurs-Hoeijmakers; Alex Hoischen; Rolph Pfundt; Nik Krumm; Gemma L Carvill; Deana Li; David Amaral; Natasha Brown; Paul J Lockhart; Ingrid E Scheffer; Antonino Alberti; Marie Shaw; Rosa Pettinato; Raymond Tervo; Nicole de Leeuw; Margot R F Reijnders; Beth S Torchia; Hilde Peeters; Brian J O'Roak; Marco Fichera; Jayne Y Hehir-Kwa; Jay Shendure; Heather C Mefford; Eric Haan; Jozef Gécz; Bert B A de Vries; Corrado Romano; Evan E Eichler
Journal:  Nat Genet       Date:  2014-09-14       Impact factor: 38.330

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  155 in total

1.  When Is a Disease a "Disease"?

Authors:  Jeffrey Bland
Journal:  Integr Med (Encinitas)       Date:  2015-12

2.  An Incomplete Understanding of Human Genetic Variation.

Authors:  John Huddleston; Evan E Eichler
Journal:  Genetics       Date:  2016-04       Impact factor: 4.562

3.  Phenome-wide Burden of Copy-Number Variation in the UK Biobank.

Authors:  Matthew Aguirre; Manuel A Rivas; James Priest
Journal:  Am J Hum Genet       Date:  2019-07-25       Impact factor: 11.025

4.  Discovery of tandem and interspersed segmental duplications using high-throughput sequencing.

Authors:  Arda Soylev; Thong Minh Le; Hajar Amini; Can Alkan; Fereydoun Hormozdiari
Journal:  Bioinformatics       Date:  2019-10-15       Impact factor: 6.937

Review 5.  Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing.

Authors:  Abdul Rezzak Hamzeh; T Daniel Andrews; Matt A Field
Journal:  Methods Mol Biol       Date:  2021

6.  Sequencing and de novo assembly of 150 genomes from Denmark as a population reference.

Authors:  Lasse Maretty; Jacob Malte Jensen; Bent Petersen; Jonas Andreas Sibbesen; Siyang Liu; Palle Villesen; Laurits Skov; Kirstine Belling; Christian Theil Have; Jose M G Izarzugaza; Marie Grosjean; Jette Bork-Jensen; Jakob Grove; Thomas D Als; Shujia Huang; Yuqi Chang; Ruiqi Xu; Weijian Ye; Junhua Rao; Xiaosen Guo; Jihua Sun; Hongzhi Cao; Chen Ye; Johan van Beusekom; Thomas Espeseth; Esben Flindt; Rune M Friborg; Anders E Halager; Stephanie Le Hellard; Christina M Hultman; Francesco Lescai; Shengting Li; Ole Lund; Peter Løngren; Thomas Mailund; Maria Luisa Matey-Hernandez; Ole Mors; Christian N S Pedersen; Thomas Sicheritz-Pontén; Patrick Sullivan; Ali Syed; David Westergaard; Rachita Yadav; Ning Li; Xun Xu; Torben Hansen; Anders Krogh; Lars Bolund; Thorkild I A Sørensen; Oluf Pedersen; Ramneek Gupta; Simon Rasmussen; Søren Besenbacher; Anders D Børglum; Jun Wang; Hans Eiberg; Karsten Kristiansen; Søren Brunak; Mikkel Heide Schierup
Journal:  Nature       Date:  2017-07-26       Impact factor: 49.962

7.  Neurons with Complex Karyotypes Are Rare in Aged Human Neocortex.

Authors:  William D Chronister; Ian E Burbulis; Margaret B Wierman; Matthew J Wolpert; Mark F Haakenson; Aiden C B Smith; Joel E Kleinman; Thomas M Hyde; Daniel R Weinberger; Stefan Bekiranov; Michael J McConnell
Journal:  Cell Rep       Date:  2019-01-22       Impact factor: 9.423

8.  Computational detection and experimental validation of segmental duplications and associated copy number variations in water buffalo ( Bubalus bubalis ).

Authors:  Shuli Liu; Xiaolong Kang; Claudia R Catacchio; Mei Liu; Lingzhao Fang; Steven G Schroeder; Wenli Li; Benjamin D Rosen; Daniela Iamartino; Leopoldo Iannuzzi; Tad S Sonstegard; Curtis P Van Tassell; Mario Ventura; Wai Yee Low; John L Williams; Derek M Bickhart; George E Liu
Journal:  Funct Integr Genomics       Date:  2019-02-07       Impact factor: 3.410

Review 9.  Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.

Authors:  G David Poznik; Yali Xue; Fernando L Mendez; Thomas F Willems; Andrea Massaia; Melissa A Wilson Sayres; Qasim Ayub; Shane A McCarthy; Apurva Narechania; Seva Kashin; Yuan Chen; Ruby Banerjee; Juan L Rodriguez-Flores; Maria Cerezo; Haojing Shao; Melissa Gymrek; Ankit Malhotra; Sandra Louzada; Rob Desalle; Graham R S Ritchie; Eliza Cerveira; Tomas W Fitzgerald; Erik Garrison; Anthony Marcketta; David Mittelman; Mallory Romanovitch; Chengsheng Zhang; Xiangqun Zheng-Bradley; Gonçalo R Abecasis; Steven A McCarroll; Paul Flicek; Peter A Underhill; Lachlan Coin; Daniel R Zerbino; Fengtang Yang; Charles Lee; Laura Clarke; Adam Auton; Yaniv Erlich; Robert E Handsaker; Carlos D Bustamante; Chris Tyler-Smith
Journal:  Nat Genet       Date:  2016-04-25       Impact factor: 38.330

10.  Selection Has Countered High Mutability to Preserve the Ancestral Copy Number of Y Chromosome Amplicons in Diverse Human Lineages.

Authors:  Levi S Teitz; Tatyana Pyntikova; Helen Skaletsky; David C Page
Journal:  Am J Hum Genet       Date:  2018-08-02       Impact factor: 11.025

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