Whole genome amplification for CGH analysis: Linker-adapter PCR as the method of choice for difficult and limited samples

Cytometry Part A

Volumn 61, Issue 1, 2004, Pages 26-34

  Pirker, Christine ^a   Raidl, Maria ^b   Steiner, Elisabeth ^a   Elbling, Leonilla ^a   Holzmann, Klaus ^a   Spiegl Kreinecker, Sabine ^a   Aubele, Michaela ^c   Grasl Kraupp, Bettina ^b   Marosi, Christine ^a   Micksche, Michael ^a   Berger, Walter ^a  

^a MEDICAL UNIVERSITY OF VIENNA   (Austria)

^b MEDICAL UNIVERSITY OF VIENNA   (Austria)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

CGH; Comparative genomic hybridization; Degenerate oligonucleotide primed PCR; Degraded DNA; DOP PCR; Linker adapter mediated PCR; Paraffin embedded tissue; Whole genome amplification

Indexed keywords

FORMALDEHYDE; PARAFFIN;

ANALYTIC METHOD; ARTICLE; CELL TYPE; CHROMOSOME 16P; CHROMOSOME 1P; CHROMOSOME 4Q; CHROMOSOME LOSS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; DEGENERATE OLIGONUCLEOTIDE PRIMED POLYMERASE CHAIN REACTION; DILUTION; DIPLOIDY; DNA DEGRADATION; DNA DETERMINATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERMETHOD COMPARISON; LABORATORY DIAGNOSIS; LINKER ADAPTER POLYMERASE CHAIN REACTION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QUALITY CONTROL; SAMPLING; TISSUE TYPES;

CELL LINE, TUMOR; CHROMOSOME ABERRATIONS; DNA, NEOPLASM; GENOME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; NUCLEIC ACID AMPLIFICATION TECHNIQUES; NUCLEIC ACID HYBRIDIZATION; POLYMERASE CHAIN REACTION;

EID: 4444226427     PISSN: 15524922     EISSN: None     Source Type: Journal    
DOI: 10.1002/cyto.a.20060     Document Type: Article

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