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Journal of Clinical Pathology 2004;57:644-646; doi:10.1136/jcp.2003.013029
Copyright © 2004 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
Journal of Clinical Pathology 2004;57:644-646
© 2004 BMJ Publishing Group Ltd & Association of Clinical Pathologists

SHORT REPORT

High resolution microarray comparative genomic hybridisation analysis using spotted oligonucleotides

B Carvalho1, E Ouwerkerk2, G A Meijer1 and B Ylstra2

1 Department of Pathology, VU University Medical Centre, de Boelelaan 1117, 1081HV Amsterdam, The Netherlands
2 Microarray Core Facility, Medical Faculty, VU University Medical Centre, van der Boechorststraat 7-9, 1081BT Amsterdam, The Netherlands

Correspondence to:
Correspondence to:
Dr B Ylstra
Microarray Core Facility, Medical Faculty, VU University Medical Centre, van der Boechorststraat 7-9, 1081BT Amsterdam, The Netherlands; b.ylstra{at}vumc.nl

ABSTRACT

Background: Currently, comparative genomic hybridisation array (array CGH) is the method of choice for studying genome wide DNA copy number changes. To date, either amplified representations of bacterial artificial chromosomes (BACs)/phage artificial chromosomes (PACs) or cDNAs have been spotted as probes. The production of BAC/PAC and cDNA arrays is time consuming and expensive.

Aim: To evaluate the use of spotted 60 mer oligonucleotides (oligos) for array CGH.

Methods: The hybridisation of tumour cell lines with known chromosomal aberrations on to either BAC or oligoarrrays that are mapped to the human genome.

Results: Oligo CGH was able to detect amplifications with high accuracy and greater spatial resolution than other currently used array CGH platforms. In addition, single copy number changes could be detected with a resolution comparable to conventional CGH.

Conclusions: Oligos are easy to handle and flexible, because they can be designed for any part of the genome without the need for laborious amplification procedures. The full genome array, containing around 30 000 oligos of all genes in the human genome, will represent a big step forward in the analysis of chromosomal copy number changes. Finally, oligoarray CGH can easily be used for any organism with a fully sequenced genome.

Keywords: omparative genomic hybridisation array; microarray; oligonucleotides

Abbreviations: BAC, bacterial artificial chromosome; CGH, comparative genomic hybridisation; CHORI, Children’s Hospital Oakland Research Institute; oligo, oligonucleotide; PAC, phage artificial chromosome; PCR, polymerase chain reaction


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