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Haplotype-aware diplotyping from noisy long reads
Current genotyping approaches for single-nucleotide variations rely on short, accurate reads from second-generation sequencing devices. Presently, third-generation sequencing platforms are rapidly becoming more widespread, yet approaches for leveraging their long but error-prone reads for genotyping...
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| Publicat a: | Genome Biol |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6547545/ https://ncbi.nlm.nih.gov/pubmed/31159868 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-019-1709-0 |
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