NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data

BACKGROUND: Structural variants (SVs) in human genomes are implicated in a variety of human diseases. Long-read sequencing delivers much longer read lengths than short-read sequencing and may greatly improve SV detection. However, due to the relatively high cost of long-read sequencing, it is unclea...

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Detalles Bibliográficos
Autores principales: Fang, Li, Hu, Jiang, Wang, Depeng, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966861/
https://www.ncbi.nlm.nih.gov/pubmed/29792160
http://dx.doi.org/10.1186/s12859-018-2207-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966861/
https://www.ncbi.nlm.nih.gov/pubmed/29792160
http://dx.doi.org/10.1186/s12859-018-2207-1

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