Across array comparative genomic hybridization: A strategy to reduce reference channel hybridizations
Autor: | Bauke Ylstra, Tineke E. Buffart, Gerrit A. Meijer, Alan Mrsić, Sjoerd J. Vosse, Marianne Tijssen, Danielle Israeli |
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Přispěvatelé: | Medical oncology, Pathology, CCA - Disease profiling |
Rok vydání: | 2008 |
Předmět: |
Chromosome Aberrations
Genetics Cancer Research Genome Human Gene Dosage Copy number analysis Nucleic Acid Hybridization Chromosome 9 DNA Neoplasm Biology Gene dosage genomic DNA Cell Line Tumor ERBB2 Gene Amplification Humans Copy-number variation Median absolute deviation Oligonucleotide Array Sequence Analysis Comparative genomic hybridization |
Zdroj: | Buffart, T E, Israeli, D, Tijssen, M, Vosse, S J, Mrsic, A, Meijer, G A & Ylstra, B 2008, ' Across array comparative genomic hybridization: a strategy to reduce reference channel hybridizations ', Genes, Chromosomes & Cancer, vol. 47, no. 11, pp. 994-1004 . https://doi.org/10.1002/gcc.20605 Genes, Chromosomes & Cancer, 47(11), 994-1004 |
ISSN: | 1098-2264 1045-2257 |
DOI: | 10.1002/gcc.20605 |
Popis: | Array comparative genomic hybridization (array CGH) is widely used for studying chromosomal copy number aberrations (CNAs) on a genome-wide and high-resolution scale in heritable disorders and cancers. The aim of this study was to test if the separate channels of dual channel arrays can be interchanged (across array) to either make array CGH more sensitive and cost effective and/or to generate profiles of CNAs and copy number variations (CNVs). Therefore the BT474 breast cancer cell line was compared with a mix of normal reference DNAs hybridized on different arrays and days and DNA copy number profiles were evaluated. Quality was assessed, using regular dual channel array CGH as a standard, using four quality measures, i.e., the median absolute deviation value of chromosome 2, the amplitude of the ERBB2 gene amplification, a deletion on chromosome 9, and the deflection on chromosome 8. The quality of the across array CGH profiles matched or even surpassed the quality of regular dual channel array CGH. In addition, this across array approach was tested for genomic DNA derived from formalin-fixed paraffin-embedded tumors tissue samples, resulting in high-quality copy number profiles, comparable to regular dual channel arrays. Finally, we demonstrated this approach to obtain both CNA and CNV profiles. In summary, across array CGH avoids redundant hybridizations of the same reference material in every experiment either allowing hybridization of two test samples on one array or producing both CNA and CNV profiles simultaneously. |
Databáze: | OpenAIRE |
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