Resolving complex structural variants via nanopore sequencing

The recent development of high-throughput sequencing platforms provided impressive insights into the field of human genetics and contributed to considering structural variants (SVs) as the hallmark of genome instability, leading to the establishment of several pathologic conditions, including neopla...

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Detalles Bibliográficos
Autores principales: Romagnoli, Simone, Bartalucci, Niccolò, Vannucchi, Alessandro Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479017/
https://www.ncbi.nlm.nih.gov/pubmed/37674481
http://dx.doi.org/10.3389/fgene.2023.1213917

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479017/
https://www.ncbi.nlm.nih.gov/pubmed/37674481
http://dx.doi.org/10.3389/fgene.2023.1213917

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