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Human cancers and some congenital traits are characterized by cytogenetic aberrations including translocations, amplifications, duplications or deletions that can involve gain or loss of genetic material. We have developed a simple method to precisely delineate such regions with known or cryptic genomic alterations. Molecular copy-number counting (MCC) uses PCR to interrogate miniscule amounts of genomic DNA and allows progressive delineation of DNA content to within a few hundred base pairs of a genomic alteration. As an example, we have located the junctions of a recurrent nonreciprocal translocation between chromosomes 3 and 5 in human renal cell carcinoma, facilitating cloning of the breakpoint without recourse to genomic libraries. The analysis also revealed additional cryptic chromosomal changes close to the translocation junction. MCC is a fast and flexible method for characterizing a wide range of chromosomal aberrations.

Original publication

DOI

10.1038/nmeth880

Type

Journal article

Journal

Nat Methods

Publication Date

06/2006

Volume

3

Pages

447 - 453

Keywords

Carcinoma, Renal Cell, Chromosome Mapping, DNA Mutational Analysis, Gene Dosage, Genetic Predisposition to Disease, Genome, Human, Haplotypes, Humans, Kidney Neoplasms, Phenotype, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Sequence Analysis, DNA