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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:BMC Syst Biol
Main Authors: Liu, Yongchao, Loewer, Martin, Aluru, Srinivas, Schmidt, Bertil
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2016
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4977481/
https://ncbi.nlm.nih.gov/pubmed/27489955
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12918-016-0300-5
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker