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Variant genotyping with gap filling

Although recent developments in DNA sequencing have allowed for great leaps in both the quality and quantity of genome assembly projects, de novo assemblies still lack the efficiency and accuracy required for studying genetic variation of individuals. Thus, efficient and accurate methods for calling...

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Detalles Bibliográficos
Autores principales: Walve, Riku, Salmela, Leena, Mäkinen, Veli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590988/
https://www.ncbi.nlm.nih.gov/pubmed/28886164
http://dx.doi.org/10.1371/journal.pone.0184608