SNVer: A statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

Nucleic Acids Research

Volumn 39, Issue 19, 2011, Pages

  Wei, Zhi ^a   Wang, Wei ^a   Hu, Pingzhao ^b   Lyon, Gholson J ^c   Hakonarson, Hakon ^c  

^a University Heights   (United States)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTICAL ERROR; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BINOMIAL BINOMIAL MODEL; DATA ANALYSIS; FALSE POSITIVE RESULT; GENE FREQUENCY; GENE LOCUS; GENETIC VARIABILITY; GENOTYPE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; NEXT GENERATION SEQUENCING; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCING ERROR; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE NUCLEOTIDE VARIANT CALLER SEEKER; SNVER; STATISTICAL ANALYSIS; STATISTICAL MODEL; COMPUTER PROGRAM; HIGH THROUGHPUT SEQUENCING;

GENE FREQUENCY; GENETIC VARIATION; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; MODELS, STATISTICAL; POLYMORPHISM, SINGLE NUCLEOTIDE; SOFTWARE;

EID: 80455129691     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkr599     Document Type: Article

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