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Gewählte Publikation:

Klein, CA; Schmidt-Kittler, O; Schardt, JA; Pantel, K; Speicher, MR; Riethmüller, G.
Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells.
Proc Natl Acad Sci U S A. 1999; 96(8):4494-4499 Doi: 10.1073/pnas.96.8.4494 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Speicher Michael
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Abstract:
A PCR strategy is described for global amplification of DNA from a single eukaryotic cell that enables the comprehensive analysis of the whole genome. By comparative genomic hybridization, not only gross DNA copy number variations, such as monosomic X and trisomic 21 in single male cells and cells from Down's syndrome patients, respectively, but multiple deletions and amplifications characteristic for human tumor cells are reliably retrieved. As a model of heterogeneous cell populations exposed to selective pressure, we have studied single micrometastatic cells isolated from bone marrow of cancer patients. The observed congruent pattern of comparative genomic hybridization data, loss of heterozygosity, and mutations as detected by sequencing attests to the technique's fidelity and demonstrates its usefulness for assessing clonal evolution of genetic variants in complex populations.
Find related publications in this database (using NLM MeSH Indexing)
Bone Marrow Cells - cytology
Breast Neoplasms - genetics
Chromosome Mapping - genetics
Chromosomes, Human, Pair 2 - genetics
DNA - chemistry
Down Syndrome - genetics
Female - genetics
Humans - genetics
In Situ Hybridization, Fluorescence - genetics
Karyotyping - genetics
Leukocytes - cytology
Loss of Heterozygosity - cytology
Male - cytology
Neoplasms - genetics
Neoplasms, Unknown Primary - genetics
Nucleic Acid Hybridization - genetics
Polymerase Chain Reaction - genetics
Restriction Mapping - genetics
Tumor Cells, Cultured - genetics

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