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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Veröffentlicht in:Genome Biol
Hauptverfasser: Jiang, Tao, Liu, Yongzhuang, Jiang, Yue, Li, Junyi, Gao, Yan, Cui, Zhe, Liu, Yadong, Liu, Bo, Wang, Yadong
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2020
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7477834/
https://ncbi.nlm.nih.gov/pubmed/32746918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-020-02107-y
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