16GT: a fast and sensitive variant caller using a 16-genotype probabilistic model

16GT is a variant caller for Illumina whole-genome and whole-exome sequencing data. It uses a new 16-genotype probabilistic model to unify single nucleotide polymorphism and insertion and deletion calling in a single variant calling algorithm. In benchmark comparisons with 5 other widely used varian...

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Detalles Bibliográficos
Autores principales: Luo, Ruibang, Schatz, Michael C., Salzberg, Steven L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570013/
https://www.ncbi.nlm.nih.gov/pubmed/28637275
http://dx.doi.org/10.1093/gigascience/gix045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570013/
https://www.ncbi.nlm.nih.gov/pubmed/28637275
http://dx.doi.org/10.1093/gigascience/gix045

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