Literature DB >> 18502942

DupMasker: a tool for annotating primate segmental duplications.

Zhaoshi Jiang1, Robert Hubley, Arian Smit, Evan E Eichler.   

Abstract

Segmental duplications (SDs) play an important role in genome rearrangement, evolution, and the copy-number variation (CNV) of primate genomes. Such sequences are difficult to detect, a priori, because they share no defining sequence features that distinguish them from unique portions of the genome. Current sequence annotation of segmental duplications requires computationally intensive, genome-wide self-comparisons that cannot be easily implemented on new data sets. Based on the successful implementation of RepeatMasker, we developed a new genome annotation tool, DupMasker. The program uses a library of nonredundant consensus sequences of human segmental duplications, wherein a majority of the ancestral origins have been determined based on comparisons to mammalian outgroup genomes. Using DupMasker, new human and nonhuman primate (NHP) sequences may be readily queried to provide details on the origin and degree of sequence identity of each duplicon. This program can be applied to delineate the order and orientation of duplicons within complex duplication blocks and used to characterize structural variation differences between sequenced human haplotypes. We predict this tool will be valuable in the annotation of large-insert sequence clones, allowing putative unique and duplicated regions of the genomes to be annotated prior to whole genome assembly comparisons.

Entities:  

Mesh:

Year:  2008        PMID: 18502942      PMCID: PMC2493431          DOI: 10.1101/gr.078477.108

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  23 in total

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

2.  Segmental duplications: organization and impact within the current human genome project assembly.

Authors:  J A Bailey; A M Yavor; H F Massa; B J Trask; E E Eichler
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

3.  Recent segmental duplications in the human genome.

Authors:  Jeffrey A Bailey; Zhiping Gu; Royden A Clark; Knut Reinert; Rhea V Samonte; Stuart Schwartz; Mark D Adams; Eugene W Myers; Peter W Li; Evan E Eichler
Journal:  Science       Date:  2002-08-09       Impact factor: 47.728

4.  Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.

Authors:  Lluis Armengol; Miguel Angel Pujana; Joseph Cheung; Stephen W Scherer; Xavier Estivill
Journal:  Hum Mol Genet       Date:  2003-07-08       Impact factor: 6.150

5.  Segmental duplications flank the multiple sclerosis locus on chromosome 17q.

Authors:  Daniel C Chen; Janna Saarela; Royden A Clark; Timo Miettinen; Anthony Chi; Evan E Eichler; Leena Peltonen; Aarno Palotie
Journal:  Genome Res       Date:  2004-07-15       Impact factor: 9.043

6.  Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.

Authors:  Zhaoshi Jiang; Haixu Tang; Mario Ventura; Maria Francesca Cardone; Tomas Marques-Bonet; Xinwei She; Pavel A Pevzner; Evan E Eichler
Journal:  Nat Genet       Date:  2007-10-07       Impact factor: 38.330

7.  Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.

Authors:  Heather C Mefford; Severine Clauin; Andrew J Sharp; Rikke S Moller; Reinhard Ullmann; Raj Kapur; Dan Pinkel; Gregory M Cooper; Mario Ventura; H Hilger Ropers; Niels Tommerup; Evan E Eichler; Christine Bellanne-Chantelot
Journal:  Am J Hum Genet       Date:  2007-09-26       Impact factor: 11.025

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.  Mapping and sequencing of structural variation from eight human genomes.

Authors:  Jeffrey M Kidd; Gregory M Cooper; William F Donahue; Hillary S Hayden; Nick Sampas; Tina Graves; Nancy Hansen; Brian Teague; Can Alkan; Francesca Antonacci; Eric Haugen; Troy Zerr; N Alice Yamada; Peter Tsang; Tera L Newman; Eray Tüzün; Ze Cheng; Heather M Ebling; Nadeem Tusneem; Robert David; Will Gillett; Karen A Phelps; Molly Weaver; David Saranga; Adrianne Brand; Wei Tao; Erik Gustafson; Kevin McKernan; Lin Chen; Maika Malig; Joshua D Smith; Joshua M Korn; Steven A McCarroll; David A Altshuler; Daniel A Peiffer; Michael Dorschner; John Stamatoyannopoulos; David Schwartz; Deborah A Nickerson; James C Mullikin; Richard K Wilson; Laurakay Bruhn; Maynard V Olson; Rajinder Kaul; Douglas R Smith; Evan E Eichler
Journal:  Nature       Date:  2008-05-01       Impact factor: 49.962

10.  Hotspots of mammalian chromosomal evolution.

Authors:  Jeffrey A Bailey; Robert Baertsch; W James Kent; David Haussler; Evan E Eichler
Journal:  Genome Biol       Date:  2004-03-08       Impact factor: 13.583

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  22 in total

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Authors:  Klaus-Peter Koepfli; Benedict Paten; Stephen J O'Brien
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Authors:  Philipp Wiemann; Christian M K Sieber; Katharina W von Bargen; Lena Studt; Eva-Maria Niehaus; Jose J Espino; Kathleen Huß; Caroline B Michielse; Sabine Albermann; Dominik Wagner; Sonja V Bergner; Lanelle R Connolly; Andreas Fischer; Gunter Reuter; Karin Kleigrewe; Till Bald; Brenda D Wingfield; Ron Ophir; Stanley Freeman; Michael Hippler; Kristina M Smith; Daren W Brown; Robert H Proctor; Martin Münsterkötter; Michael Freitag; Hans-Ulrich Humpf; Ulrich Güldener; Bettina Tudzynski
Journal:  PLoS Pathog       Date:  2013-06-27       Impact factor: 6.823

3.  A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.

Authors:  Francesca Antonacci; Jeffrey M Kidd; Tomas Marques-Bonet; Brian Teague; Mario Ventura; Santhosh Girirajan; Can Alkan; Catarina D Campbell; Laura Vives; Maika Malig; Jill A Rosenfeld; Blake C Ballif; Lisa G Shaffer; Tina A Graves; Richard K Wilson; David C Schwartz; Evan E Eichler
Journal:  Nat Genet       Date:  2010-08-22       Impact factor: 38.330

4.  Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions.

Authors:  Stefan Kirsch; Claudia Münch; Zhaoshi Jiang; Ze Cheng; Lin Chen; Christiane Batz; Evan E Eichler; Werner Schempp
Journal:  Genome Res       Date:  2008-04-29       Impact factor: 9.043

5.  Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites.

Authors:  Santhosh Girirajan; Lin Chen; Tina Graves; Tomas Marques-Bonet; Mario Ventura; Catrina Fronick; Lucinda Fulton; Mariano Rocchi; Robert S Fulton; Richard K Wilson; Elaine R Mardis; Evan E Eichler
Journal:  Genome Res       Date:  2008-11-24       Impact factor: 9.043

6.  A human genome structural variation sequencing resource reveals insights into mutational mechanisms.

Authors:  Jeffrey M Kidd; Tina Graves; Tera L Newman; Robert Fulton; Hillary S Hayden; Maika Malig; Joelle Kallicki; Rajinder Kaul; Richard K Wilson; Evan E Eichler
Journal:  Cell       Date:  2010-11-24       Impact factor: 41.582

7.  Genome sequence and analysis of the tuber crop potato.

Authors:  Xun Xu; Shengkai Pan; Shifeng Cheng; Bo Zhang; Desheng Mu; Peixiang Ni; Gengyun Zhang; Shuang Yang; Ruiqiang Li; Jun Wang; Gisella Orjeda; Frank Guzman; Michael Torres; Roberto Lozano; Olga Ponce; Diana Martinez; Germán De la Cruz; S K Chakrabarti; Virupaksh U Patil; Konstantin G Skryabin; Boris B Kuznetsov; Nikolai V Ravin; Tatjana V Kolganova; Alexey V Beletsky; Andrei V Mardanov; Alex Di Genova; Daniel M Bolser; David M A Martin; Guangcun Li; Yu Yang; Hanhui Kuang; Qun Hu; Xingyao Xiong; Gerard J Bishop; Boris Sagredo; Nilo Mejía; Wlodzimierz Zagorski; Robert Gromadka; Jan Gawor; Pawel Szczesny; Sanwen Huang; Zhonghua Zhang; Chunbo Liang; Jun He; Ying Li; Ying He; Jianfei Xu; Youjun Zhang; Binyan Xie; Yongchen Du; Dongyu Qu; Merideth Bonierbale; Marc Ghislain; Maria del Rosario Herrera; Giovanni Giuliano; Marco Pietrella; Gaetano Perrotta; Paolo Facella; Kimberly O'Brien; Sergio E Feingold; Leandro E Barreiro; Gabriela A Massa; Luis Diambra; Brett R Whitty; Brieanne Vaillancourt; Haining Lin; Alicia N Massa; Michael Geoffroy; Steven Lundback; Dean DellaPenna; C Robin Buell; Sanjeev Kumar Sharma; David F Marshall; Robbie Waugh; Glenn J Bryan; Marialaura Destefanis; Istvan Nagy; Dan Milbourne; Susan J Thomson; Mark Fiers; Jeanne M E Jacobs; Kåre L Nielsen; Mads Sønderkær; Marina Iovene; Giovana A Torres; Jiming Jiang; Richard E Veilleux; Christian W B Bachem; Jan de Boer; Theo Borm; Bjorn Kloosterman; Herman van Eck; Erwin Datema; Bas te Lintel Hekkert; Aska Goverse; Roeland C H J van Ham; Richard G F Visser
Journal:  Nature       Date:  2011-07-10       Impact factor: 49.962

8.  Primate segmental duplication creates novel promoters for the LRRC37 gene family within the 17q21.31 inversion polymorphism region.

Authors:  Cemalettin Bekpen; Ibrahim Tastekin; Priscillia Siswara; Cezmi A Akdis; Evan E Eichler
Journal:  Genome Res       Date:  2012-03-14       Impact factor: 9.043

9.  Characterization of six human disease-associated inversion polymorphisms.

Authors:  Francesca Antonacci; Jeffrey M Kidd; Tomas Marques-Bonet; Mario Ventura; Priscillia Siswara; Zhaoshi Jiang; Evan E Eichler
Journal:  Hum Mol Genet       Date:  2009-04-21       Impact factor: 6.150

10.  A burst of segmental duplications in the genome of the African great ape ancestor.

Authors:  Tomas Marques-Bonet; Jeffrey M Kidd; Mario Ventura; Tina A Graves; Ze Cheng; LaDeana W Hillier; Zhaoshi Jiang; Carl Baker; Ray Malfavon-Borja; Lucinda A Fulton; Can Alkan; Gozde Aksay; Santhosh Girirajan; Priscillia Siswara; Lin Chen; Maria Francesca Cardone; Arcadi Navarro; Elaine R Mardis; Richard K Wilson; Evan E Eichler
Journal:  Nature       Date:  2009-02-12       Impact factor: 49.962

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