SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations

BACKGROUND: Various approaches to calling single-nucleotide variants (SNVs) or insertion-or-deletion (indel) mutations have been developed based on next-generation sequencing (NGS). However, most of them are dedicated to a particular type of mutation, e.g. germline SNVs in normal cells, somatic SNVs...

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Detalles Bibliográficos
Autores principales: Liu, Yongchao, Loewer, Martin, Aluru, Srinivas, Schmidt, Bertil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977481/
https://www.ncbi.nlm.nih.gov/pubmed/27489955
http://dx.doi.org/10.1186/s12918-016-0300-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977481/
https://www.ncbi.nlm.nih.gov/pubmed/27489955
http://dx.doi.org/10.1186/s12918-016-0300-5

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