Long‐read Oxford nanopore sequencing reveals a de novo case of complex chromosomal rearrangement involving chromosomes 2, 7, and 13
Author:
Affiliation:
1. Department of Obstetrics and Gynaecology West China Second University Hospital, Sichuan University Chengdu China
2. Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education Sichuan University Chengdu China
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2011
Reference25 articles.
1. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
2. Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications
3. Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome
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