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

BMC Systems Biology

Volumn 10, Issue , 2016, Pages

  Liu, Yongchao ^a   Loewer, Martin ^b   Aluru, Srinivas ^a   Schmidt, Bertil ^c  

^a Georgia Institute of Technology   (United States)

^b UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

^c JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

Bayesian model; Indel calling; SNP calling; Somatic SNV calling

Indexed keywords

ALGORITHM; BIOLOGY; CYSTADENOCARCINOMA; FEMALE; GENE FREQUENCY; GENETICS; GERM CELL; HIGH THROUGHPUT SEQUENCING; HUMAN; INDEL MUTATION; METABOLISM; OVARY TUMOR; PATHOLOGY; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM;

ALGORITHMS; COMPUTATIONAL BIOLOGY; CYSTADENOCARCINOMA, SEROUS; FEMALE; GENE FREQUENCY; GERM CELLS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INDEL MUTATION; OVARIAN NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84979879819     PISSN: None     EISSN: 17520509     Source Type: Journal    
DOI: 10.1186/s12918-016-0300-5     Document Type: Article

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