Challenges in identifying large germline structural variants for clinical use by long read sequencing

Genomic structural variations, previously considered rare events, are widely recognized as a major source of inter-individual variability and hence, a major hurdle in optimum patient stratification and disease management. Herein, we focus on large complex germline structural variations and present c...

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Detalles Bibliográficos
Autores principales: Jenko Bizjan, Barbara, Katsila, Theodora, Tesovnik, Tine, Šket, Robert, Debeljak, Maruša, Matsoukas, Minos Timotheos, Kovač, Jernej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026727/
https://www.ncbi.nlm.nih.gov/pubmed/32099591
http://dx.doi.org/10.1016/j.csbj.2019.11.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026727/
https://www.ncbi.nlm.nih.gov/pubmed/32099591
http://dx.doi.org/10.1016/j.csbj.2019.11.008

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