Reducing INDEL calling errors in whole genome and exome sequencing data

Genome Medicine

Volumn 6, Issue 10, 2014, Pages

  Fang, Han ^a,b   Wu, Yiyang ^a,b   Narzisi, Giuseppe ^a,c   O'Rawe, Jason A ^a,b   Barrón, Laura T Jimenez ^a,d   Rosenbaum, Julie ^a   Ronemus, Michael ^a   Iossifov, Ivan ^a   Schatz, Michael C ^a   Lyon, Gholson J ^a,b  

^a Howard Hughes Medical Institute Cold Spring Harbor Laboratory Cold Spring Harbor   (United States)

^b STONY BROOK UNIVERSITY   (United States)

^c NEW YORK GENOME CENTER   (United States)

^d INSTITUTO DE CIENCIAS FÍSICAS   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

POLYMER;

ALGORITHM; AMPLICON; ARTICLE; BASE PAIRING; CONTROLLED STUDY; GENE LOCUS; GENETIC PROCEDURES; GENOME; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INDEL MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SHORT TANDEM REPEAT; SIMULATION; WHOLE EXOME SEQUENCING; WHOLE GENOME SEQUENCING; ZYGOSITY;

EID: 84921850275     PISSN: None     EISSN: 1756994X     Source Type: Journal    
DOI: 10.1186/s13073-014-0089-z     Document Type: Article

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