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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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Podrobná bibliografie
Vydáno v:Front Genet
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2020
Témata:
On-line přístup: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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