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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...
Uloženo v:
| Vydáno v: | Genome Biol |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| 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 |
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