Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot

PLoS ONE

Volumn 9, Issue 1, 2014, Pages

  Bansal, Vikas ^a,b   Dorn, Cornelia ^a,b   Grunert, Marcel ^a   Klaassen, Sabine ^a,c   Hetzer, Roland ^d   Berger, Felix ^a,d   Sperling, Silke R ^a,b  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b FREIE UNIVERSITÄT BERLIN   (Germany)

^c Department of Biology Chemistry and Pharmacy Free University of Berlin ^*  (Germany)

^d DEUTSCHES HERZZENTRUM BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH1 RECEPTOR;

ARTICLE; CLINICAL ARTICLE; COHORT ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; EXOME; FALLOT TETRALOGY; GENE; GENE DOSAGE; GENE SEQUENCE; GENETIC PROCEDURES; HAPLOTYPE MAP; HIDDEN MARKOV MODEL; HUMAN; HUMAN TISSUE; INTERMETHOD COMPARISON; ISL1 GENE; NOTCH1 GENE; POLYMERASE CHAIN REACTION; PRODH GENE; TARGETED RESEQUENCING;

ALGORITHMS; COMPUTATIONAL BIOLOGY; DNA COPY NUMBER VARIATIONS; EXOME; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MARKOV CHAINS; SEQUENCE ANALYSIS, DNA; TETRALOGY OF FALLOT;

EID: 84896469057     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0085375     Document Type: Article

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