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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2016
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| Materias: | |
| 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 |