LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data

Linked-read sequencing provides long-range information on short-read sequencing data by barcoding reads originating from the same DNA molecule, and can improve detection and breakpoint identification for structural variants (SVs). Here we present LinkedSV for SV detection on linked-read sequencing d...

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Detalles Bibliográficos
Autores principales: Fang, Li, Kao, Charlly, Gonzalez, Michael V., Mafra, Fernanda A., Pellegrino da Silva, Renata, Li, Mingyao, Wenzel, Sören-Sebastian, Wimmer, Katharina, Hakonarson, Hakon, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898185/
https://www.ncbi.nlm.nih.gov/pubmed/31811119
http://dx.doi.org/10.1038/s41467-019-13397-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898185/
https://www.ncbi.nlm.nih.gov/pubmed/31811119
http://dx.doi.org/10.1038/s41467-019-13397-7

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