Detection of Structural Variations and Fusion Genes in Breast Cancer Samples Using Third-Generation Sequencing

Background: Structural variations (SVs) are common genetic alterations in the human genome that could cause different phenotypes and diseases, including cancer. However, the detection of structural variations using the second-generation sequencing was limited by its short read length, which restrain...

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Detalles Bibliográficos
Autores principales: Hu, Taobo, Li, Jingjing, Long, Mengping, Wu, Jinbo, Zhang, Zhen, Xie, Fei, Zhao, Jin, Yang, Houpu, Song, Qianqian, Lian, Sheng, Shi, Jiandong, Guo, Xueyu, Yuan, Daoli, Lang, Dandan, Yu, Guoliang, Liang, Baosheng, Zhou, Xiaohua, Ishibashi, Toyotaka, Fan, Xiaodan, Yu, Weichuan, Wang, Depeng, Wang, Yang, Peng, I-Feng, Wang, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043247/
https://www.ncbi.nlm.nih.gov/pubmed/35493102
http://dx.doi.org/10.3389/fcell.2022.854640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043247/
https://www.ncbi.nlm.nih.gov/pubmed/35493102
http://dx.doi.org/10.3389/fcell.2022.854640

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