Application of long-read sequencing to the detection of structural variants in human cancer genomes

In recent years, the so-called long-read sequencing technology has had a substantial impact on various aspects of genome sciences. Here, we introduce recent studies of cancerous structural variants (SVs) using long-read sequencing technologies, namely Pacific Biosciences (PacBio) sequencers, Oxford...

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Detalles Bibliográficos
Autores principales: Sakamoto, Yoshitaka, Zaha, Suzuko, Suzuki, Yutaka, Seki, Masahide, Suzuki, Ayako
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350331/
https://www.ncbi.nlm.nih.gov/pubmed/34527193
http://dx.doi.org/10.1016/j.csbj.2021.07.030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350331/
https://www.ncbi.nlm.nih.gov/pubmed/34527193
http://dx.doi.org/10.1016/j.csbj.2021.07.030

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