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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...

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Detalles Bibliográficos
Autores principales: Monsu, Maurilio, Comin, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2021
Materias:
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