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Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform

Genomic structural variants, including translocations, inversions, insertions, deletions, and duplications, are challenging to be reliably detected by traditional genomic technologies. In particular, balanced translocations and inversions can neither be identified by microarrays since they do not al...

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Detalles Bibliográficos
Publicado en:Front Genet
Main Authors: Hu, Liang, Liang, Fan, Cheng, Dehua, Zhang, Zhiyuan, Yu, Guoliang, Zha, Jianjun, Wang, Yang, Xia, Qi, Yuan, Daoli, Tan, Yueqiu, Wang, Depeng, Liang, Yu, Lin, Ge
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6972507/
https://ncbi.nlm.nih.gov/pubmed/32010185
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.01313
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