Digital karyotyping
- 2 December 2002
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 99 (25) , 16156-16161
- https://doi.org/10.1073/pnas.202610899
Abstract
Alterations in the genetic content of a cell are the underlying cause of many human diseases, including cancers. We have developed a method, called digital karyotyping, that provides quantitative analysis of DNA copy number at high resolution. This approach involves the isolation and enumeration of short sequence tags from specific genomic loci. Analysis of human cancer cells by using this method identified gross chromosomal changes as well as amplifications and deletions, including regions not previously known to be altered. Foreign DNA sequences not present in the normal human genome could also be readily identified. Digital karyotyping provides a broadly applicable means for systematic detection of DNA copy number changes on a genomic scale.Keywords
This publication has 27 references indexed in Scilit:
- Genomic Signature Tags (GSTs): A System for Profiling Genomic DNAGenome Research, 2002
- Using the transcriptome to annotate the genomeNature Biotechnology, 2002
- Treaty Draft Raises Scientific HacklesScience, 1996
- Multicolor Spectral Karyotyping of Human ChromosomesScience, 1996
- Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancersNature Genetics, 1996
- Karyotyping human chromosomes by combinatorial multi-fluor FISHNature Genetics, 1996
- Serial Analysis of Gene ExpressionScience, 1995
- Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid TumorsScience, 1992
- Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal CancersScience, 1991
- Extrachromosomal amplification of the epidermal growth factor receptor gene in a human colon carcinoma cell lineGenes, Chromosomes and Cancer, 1991