Načítá se...

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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Genome Biol
Hlavní autoři: Jiang, Tao, Liu, Yongzhuang, Jiang, Yue, Li, Junyi, Gao, Yan, Cui, Zhe, Liu, Yadong, Liu, Bo, Wang, Yadong
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!