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Dysgu: efficient structural variant calling using short or long reads
Structural variation (SV) plays a fundamental role in genome evolution and can underlie inherited or acquired diseases such as cancer. Long-read sequencing technologies have led to improvements in the characterization of structural variants (SVs), although paired-end sequencing offers better scalabi...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122538/ https://www.ncbi.nlm.nih.gov/pubmed/35100420 http://dx.doi.org/10.1093/nar/gkac039 |