Long-read-based human genomic structural variation detection with cuteSV

Long-read sequencing is promising for the comprehensive discovery of structural variations (SVs). However, it is still non-trivial to achieve high yields and performance simultaneously due to the complex SV signatures implied by noisy long reads. We propose cuteSV, a sensitive, fast, and scalable lo...

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Detalles Bibliográficos
Autores principales: Jiang, Tao, Liu, Yongzhuang, Jiang, Yue, Li, Junyi, Gao, Yan, Cui, Zhe, Liu, Yadong, Liu, Bo, Wang, Yadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477834/
https://www.ncbi.nlm.nih.gov/pubmed/32746918
http://dx.doi.org/10.1186/s13059-020-02107-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477834/
https://www.ncbi.nlm.nih.gov/pubmed/32746918
http://dx.doi.org/10.1186/s13059-020-02107-y

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