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Dysgu: efficient structural variant calling using short or long reads

Structural variation (SV) plays a fundamental role in genome evolution and can underlie inherited or acquired diseases such as cancer. Long-read sequencing technologies have led to improvements in the characterization of structural variants (SVs), although paired-end sequencing offers better scalabi...

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Detalles Bibliográficos
Autores principales: Cleal, Kez, Baird, Duncan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122538/
https://www.ncbi.nlm.nih.gov/pubmed/35100420
http://dx.doi.org/10.1093/nar/gkac039