Inferring copy number and genotype in tumour exome data

BMC Genomics

Volumn 15, Issue 1, 2014, Pages

  Amarasinghe, Kaushalya C ^a   Li, Jason ^a,b   Hunter, Sally M ^b   Ryland, Georgina L ^b   Cowin, Prue A ^b   Campbell, Ian G ^b,c   Halgamuge, Saman K ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

^b PETER MACCALLUM CANCER CENTRE   (Australia)

^c UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

AFFYMETRIX SNP 6.0; ANEUPLOIDY; ARTICLE; COMPUTER PROGRAM; CONTROLLED STUDY; COPY NUMBER VARIATION; FALSE POSITIVE RESULT; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ALGORITHM; GENETIC PROCEDURES; GENOTYPE; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MEASUREMENT ACCURACY; MEASUREMENT PRECISION; POLYPLOIDY; PREDICTIVE VALUE; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM; TETRAPLOIDY; TRIPLOIDY; ALGORITHM; BIOLOGY; CHROMOSOME ABERRATION; EXOME; GENETICS; GENOMICS; GENOTYPING TECHNIQUE; HIGH THROUGHPUT SEQUENCING; NEOPLASM; OVARY TUMOR; PROCEDURES; REPRODUCIBILITY;

ALGORITHMS; CHROMOSOME ABERRATIONS; COMPUTATIONAL BIOLOGY; DNA COPY NUMBER VARIATIONS; EXOME; FEMALE; GENOMICS; GENOTYPE; GENOTYPING TECHNIQUES; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; LOSS OF HETEROZYGOSITY; NEOPLASMS; OVARIAN NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE; POLYPLOIDY; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY;

EID: 84908059304     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-15-732     Document Type: Article

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