Detecting copy number status and uncovering subclonal markers in heterogeneous tumor biopsies

BMC Genomics

Volumn 12, Issue , 2011, Pages

  Parisi, Fabio ^a   Ariyan, Stephan ^b   Narayan, Deepak ^b   Bacchiocchi, Antonella ^b   Hoyt, Kathleen ^b   Cheng, Elaine ^b   Xu, Fang ^b   Li, Peining ^b   Halaban, Ruth ^b   Kluger, Yuval ^a  

^a YALE CANCER CENTER   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Copy number SNP arrays; Melanoma; Next generation sequencing

Indexed keywords

TRANSCRIPTION FACTOR EZH2; TRANSCRIPTOME; TUMOR MARKER;

ALLELIC IMBALANCE; ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; E2F8 GENE; ETV4 GENE; EZH2 GENE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENETIC HETEROGENEITY; GENETIC REGULATION; HUMAN; HUMAN CELL; MELANOMA CELL; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; TRANSCRIPTOMICS; TUMOR BIOPSY; TUMOR GENE; ALLELE; BIOLOGY; GENE DOSAGE; GENETICS; GENOTYPE; HIGH THROUGHPUT SEQUENCING; METHODOLOGY; NEOPLASM; PATHOLOGY; REPRODUCIBILITY; TUMOR CELL LINE;

ALLELES; CELL LINE, TUMOR; COMPUTATIONAL BIOLOGY; DNA COPY NUMBER VARIATIONS; GENE DOSAGE; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; NEOPLASMS; REPRODUCIBILITY OF RESULTS; TUMOR MARKERS, BIOLOGICAL;

EID: 79955762549     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-12-230     Document Type: Article

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