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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Publicado no:Nat Commun
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6898185/
https://ncbi.nlm.nih.gov/pubmed/31811119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-13397-7
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