Continuing difficulties in interpreting CNV data: Lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

BMC Medical Genomics

Volumn 6, Issue 1, 2013, Pages

  Talseth Palmer, Bente A ^a,b   Holliday, Elizabeth G ^b,c   Evans, Tiffany Jane ^a,b   McEvoy, Mark ^c   Attia, John ^c   Grice, Desma M ^a,b,d   Masson, Amy L ^a,b   Meldrum, Cliff ^e   Spigelman, Allan ^f,g   Scott, Rodney J ^a,b,e  

^a UNIVERSITY OF NEWCASTLE   (Australia)

^b JOHN HUNTER HOSPITAL   (Australia)

^c UNIVERSITY OF NEWCASTLE   (Australia)

^d CSIRO   (Australia)

^e JOHN HUNTER HOSPITAL   (Australia)

^f UNIVERSITY OF NEW SOUTH WALES   (Australia)

^g Hunter Family Cancer Service   (Australia)

Author keywords

CNV burden; CNVs; HNPCC; Lynch syndrome; SNP arrays

Indexed keywords

PROTEIN MLH1; PROTEIN MSH2;

ARTICLE; AUSTRALIA; CANCER PATIENT; CHROMOSOME 16P; CHROMOSOME 7Q; CHROMOSOME ADDITION; CONTROLLED STUDY; COPY NUMBER VARIATION; CPG ISLAND; FALSE POSITIVE RESULT; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOMIC INSTABILITY; GENOTYPE; HEREDITARY NONPOLYPOSIS COLORECTAL CANCER; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TUMOR VOLUME;

ALLELES; AUSTRALIA; CHROMOSOMES, HUMAN, PAIR 7; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA COPY NUMBER VARIATIONS; DNA REPAIR; GENE FREQUENCY; GENETIC LOCI; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; GENOMIC INSTABILITY; GENOTYPE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SOFTWARE;

EID: 84875306095     PISSN: None     EISSN: 17558794     Source Type: Journal    
DOI: 10.1186/1755-8794-6-10     Document Type: Article

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