High-Resolution Breakpoint Analysis Provides Evidence for the Sequence-Directed Nature of Genome Rearrangements in Hereditary Disorders-Reference-Cited by-同舟云学术

High-Resolution Breakpoint Analysis Provides Evidence for the Sequence-Directed Nature of Genome Rearrangements in Hereditary Disorders

Published:2015-02 Issue:2 Volume:36 Page:250-259
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Kovac Michal B.¹²³,Kovacova Monika⁴,Bachraty Hynek⁵,Bachrata Katarina⁶,Piscuoglio Salvatore¹²⁷,Hutter Pierre⁸,Ilencikova Denisa⁹,Bartosova Zdena¹⁰,Tomlinson Ian³,Roethlisberger Benno¹¹,Heinimann Karl¹²

Affiliation:

1. Research Group Human Genomics; Department of Biomedicine; University of Basel; Basel Switzerland

2. Medical Genetics; University Hospital Basel; Basel Switzerland

3. The Wellcome Trust Centre for Human Genetics; University of Oxford; Old Road Campus Oxford UK

4. Institute of Mathematics and Physics; Faculty of Mechanical Engineering; Slovak University of Technology; Bratislava Slovakia

5. Department of Software Technologies; Faculty of Management Science and Informatics; University of Zilina; Zilina Slovakia

6. Department of InfoCom Networks; Faculty of Management Science and Informatics; University of Zilina; Zilina Slovakia

7. Department of Pathology; Memorial Sloan-Kettering Cancer Center; New York City New York

8. Institut Central des Hôpitaux Valaisans; Service de Génétique Médicale; Sion Switzerland

9. Pediatric Department; University Children Hospital; Comenius University; Bratislava Slovakia

10. Medical Genetics; St. Elizabeth Cancer Institute; Bratislava Slovakia

11. Kantonsspital Aarau; Tellstrasse; Aarau Switzerland

Funder

Freie Akademische Gesellschaft Basel

Huggenberger-Bischoff Foundation

Krebsliga beider Basel

Krebsliga Zentralschweiz

Slovak Research and Development Agency

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22734/fullpdf

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3. Breakpoints of gross deletions coincide with non-B DNA conformations;Bacolla;Proc Natl Acad Sci USA,2004

4. DREME: motif discovery in transcription factor ChIP-seq data;Bailey;Bioinformatics,2011

5. MEME SUITE: tools for motif discovery and searching;Bailey;Nucleic Acids Res,2009

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