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NanoVar: accurate characterization of patients’ genomic structural variants using low-depth nanopore sequencing
The recent advent of third-generation sequencing technologies brings promise for better characterization of genomic structural variants by virtue of having longer reads. However, long-read applications are still constrained by their high sequencing error rates and low sequencing throughput. Here, we...
| Autores principales: | , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055087/ https://www.ncbi.nlm.nih.gov/pubmed/32127024 http://dx.doi.org/10.1186/s13059-020-01968-7 |