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Fast alignment of reads to a variation graph with application to SNP detection
Sequencing technologies has provided the basis of most modern genome sequencing studies due to its high base-level accuracy and relatively low cost. One of the most demanding step is mapping reads to the human reference genome. The reliance on a single reference human genome could introduce substant...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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De Gruyter
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709736/ https://www.ncbi.nlm.nih.gov/pubmed/34783230 http://dx.doi.org/10.1515/jib-2021-0032 |