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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...
Gorde:
| Argitaratua izan da: | Genome Biol |
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| Egile Nagusiak: | , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2020
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| Gaiak: | |
| Sarrera elektronikoa: | 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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