Identification of copy number variants from exome sequence data

BMC Genomics

Volumn 15, Issue 1, 2014, Pages

  Samarakoon, Pubudu Saneth ^a,b   Sorte, Hanne Sørmo ^a,b   Kristiansen, Bjørn Evert ^b   Skodje, Tove ^b   Sheng, Ying ^b   Tjønnfjord, Geir E ^a,b   Stadheim, Barbro ^b   Stray Pedersen, Asbjørg ^b,c,d   Rødningen, Olaug Kristin ^b   Lyle, Robert ^a,b  

^a UNIVERSITY OF OSLO   (Norway)

^b OSLO UNIVERSITY HOSPITAL   (Norway)

^c TEXAS CHILDREN S HOSPITAL   (United States)

^d BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

CNV prediction; Custom aCGH; Exome

Indexed keywords

ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER PREDICTION; COMPUTER PROGRAM; CONTROLLED STUDY; COPY NUMBER VARIATION; EXOME; EXON; FALSE POSITIVE RESULT; GENE SEQUENCE; HUMAN; INTERMETHOD COMPARISON; MUTATIONAL ANALYSIS; SENSITIVITY AND SPECIFICITY; ALGORITHM; DNA MICROARRAY; FEMALE; GENETICS; GENOMICS; MALE; MUTATION; PROCEDURES;

ALGORITHMS; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; EXOME; EXONS; FEMALE; GENOMICS; HUMANS; MALE; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;

EID: 84905828993     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-15-661     Document Type: Article

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