Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays

Genome Research

Volumn 10, Issue 8, 2000, Pages 1126-1137

  Mei, Rui ^a   Galipeau, Patricia C ^b   Prass, Cynthia ^c   Berno, Anthony ^a   Ghandour, Ghassan ^d   Patil, Nila ^a   Wolff, Roger K ^c   Chee, Mark S ^e   Reid, Brian J ^b   Lockhart, David J ^a,f  

^a Thermo Fisher Scientific   (United States)

^b Fred Hutchinson Cancer Research Center   (United States)

^c Mercator Genetics Inc   (United States)

^d Eos Biotechnology   (United States)

^e ILLUMINA INC   (United States)

^f GENOMICS INSTITUTE OF THE NOVARTIS RESEARCH FOUNDATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; OLIGONUCLEOTIDE;

ALLELE; ANALYTIC METHOD; ARTICLE; CELL POPULATION; CHROMOSOME; CLINICAL ARTICLE; CONTROLLED STUDY; DENSITY; DIAGNOSTIC VALUE; DNA PROBE; ESOPHAGUS CARCINOMA; GENE LOCUS; GENETIC ANALYSIS; GENOME; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; PRIORITY JOURNAL; PROGNOSIS; REPRODUCIBILITY; SINGLE NUCLEOTIDE POLYMORPHISM; TUMOR;

ADENOCARCINOMA; ALLELES; CHILD; DNA MUTATIONAL ANALYSIS; ESOPHAGEAL NEOPLASMS; GENE AMPLIFICATION; HUMANS; LOSS OF HETEROZYGOSITY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROGNOSIS; REPRODUCIBILITY OF RESULTS;

EID: 0033832677     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.10.8.1126     Document Type: Article

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