VarBin, a novel method for classifying true and false positive variants in NGS data

BMC Bioinformatics

Volumn 14, Issue SUPPL13, 2013, Pages

  Durtschi, Jacob ^a   Margraf, Rebecca L ^a   Coonrod, Emily M ^a   Mallempati, Kalyan C ^a   Voelkerding, Karl V ^a,b  

^a ARUP INSTITUTE FOR CLINICAL AND EXPERIMENTAL PATHOLOGY   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALIGNMENT ERROR; FALSE POSITIVE; GENETIC DISEASE; GENOME ANALYSIS; LIKELIHOOD RATIOS; MOST LIKELY; SANGER SEQUENCING; SCREENING PROCESS;

ALIGNMENT; DIAGNOSIS; GENES;

BINS;

ARTICLE; CLUSTER ANALYSIS; COMPUTER PROGRAM; DNA SEQUENCE; EXOME; FEMALE; GENE LIBRARY; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETICS; GENOME; HETEROZYGOTE; HUMAN; MALE; METHODOLOGY; PEDIGREE; PREDICTIVE VALUE; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL;

CLUSTER ANALYSIS; EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME; GENOMIC LIBRARY; HETEROZYGOTE; HUMANS; LIKELIHOOD FUNCTIONS; MALE; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREDICTIVE VALUE OF TESTS; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 84886795103     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-14-S13-S2     Document Type: Article

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