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Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation
BACKGROUND: With the rapid development of long-read sequencing technologies, it is possible to reveal the full spectrum of genetic structural variation (SV). However, the expensive cost, finite read length and high sequencing error for long-read data greatly limit the widespread adoption of SV calli...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588741/ https://www.ncbi.nlm.nih.gov/pubmed/34772337 http://dx.doi.org/10.1186/s12859-021-04422-y |