Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification-Reference-Cited by-同舟云学术

Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification

Published:2017-09-22 Issue:12 Volume:38 Page:1711-1722
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Hillmer Morten¹,Summerer Anna¹,Mautner Victor-Felix²,Högel Josef¹,Cooper David N.³,Kehrer-Sawatzki Hildegard¹^ORCID

Affiliation:

1. Institute of Human Genetics; University of Ulm; Ulm Germany

2. Department of Neurology; University Hospital Hamburg Eppendorf; Hamburg Germany

3. Institute of Medical Genetics; School of Medicine; Cardiff University; Cardiff UK

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference79 articles.

1. Translocation and gross deletion breakpoints in human inherited disease and cancer. I: Nucleotide composition and recombination-associated motifs;Abeysinghe;Human Mutation,2003

2. Characterization of six human disease-associated inversion polymorphisms;Antonacci;Human Molecular Genetics,2009

3. A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk;Antonacci;Nature Genetics,2010

4. Crossovers are associated with mutation and biased gene conversion at recombination hotspots;Arbeithuber;Proceedings of the National Academy of Sciences in the United States of America,2015

5. Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination;Badge;Human Molecular Genetics,2000

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