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Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes
Haplotypes are often critical for the interpretation of genetic laboratory observations into medically actionable findings. Current massively parallel DNA sequencing technologies produce short sequence reads that are often unable to resolve haplotype information. Phasing short read data typically re...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
F1000Research
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392832/ https://www.ncbi.nlm.nih.gov/pubmed/25901276 http://dx.doi.org/10.12688/f1000research.6037.2 |