Published online 26 January 2006
Survey and Summary |
BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)
Department of Pathology, VU University Medical Center PO Box 7057, 1007 MB Amsterdam, The Netherlands 1Department of Otolaryngology/Head-Neck Surgery, VU University Medical Center PO Box 7057, 1007 MB Amsterdam, The Netherlands
*To whom correspondence should be addressed. Tel: +31 20 444 8299; Fax: +31 20 444 8318; Email: b.ylstra{at}vumc.nl
Received October 24, 2005. Revised December 8, 2005. Accepted January 4, 2006.
The array CGH technique (Array Comparative Genome Hybridization) has been developed to detect chromosomal copy number changes on a genome-wide and/or high-resolution scale. It is used in human genetics and oncology, with great promise for clinical application. Until recently primarily PCR amplified bacterial artificial chromosomes (BACs) or cDNAs have been spotted as elements on the array. The large-scale DNA isolations or PCR amplifications of the large-insert clones necessary for manufacturing the arrays are elaborate and time-consuming. Lack of a high-resolution highly sensitive (commercial) alternative has undoubtedly hindered the implementation of array CGH in research and diagnostics. Recently, synthetic oligonucleotides as arrayed elements have been introduced as an alternative substrate for array CGH, both by academic institutions as well as by commercial providers. Oligonucleotide libraries or ready-made arrays can be bought off-the-shelf saving considerable time and efforts. For RNA expression profiling, we have seen a gradual transition from in-house printed cDNA-based expression arrays to oligonucleotide arrays and we expect a similar transition for array CGH. This review compares the different platforms and will attempt to shine a light on the BAC to the future of the array CGH technique.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
D. H. Ledbetter Cytogenetic Technology -- Genotype and Phenotype N. Engl. J. Med., September 10, 2008; (2008) NEJMe0806570v1. [Full Text] [PDF] |
||||
![]() |
P. Cahan, L. E. Godfrey, P. S. Eis, T. A. Richmond, R. R. Selzer, M. Brent, H. L. McLeod, T. J. Ley, and T. A. Graubert wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data Nucleic Acids Res., April 1, 2008; 36(7): e41 - e41. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Rigaill, P. Hupe, A. Almeida, P. La Rosa, J.-P. Meyniel, C. Decraene, and E. Barillot ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays Bioinformatics, March 15, 2008; 24(6): 768 - 774. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Scheinin, S. Myllykangas, I. Borze, T. Bohling, S. Knuutila, and J. Saharinen CanGEM: mining gene copy number changes in cancer Nucleic Acids Res., January 11, 2008; 36(suppl_1): D830 - D835. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. B. Dopman and D. L. Hartl A portrait of copy-number polymorphism in Drosophila melanogaster PNAS, December 11, 2007; 104(50): 19920 - 19925. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Shen, D. T. Miller, S. W. Cheung, V. Lip, X. Sheng, K. Tomaszewicz, H. Shao, H. Fang, H. S. Tang, M. Irons, et al. Development of a Focused Oligonucleotide-Array Comparative Genomic Hybridization Chip for Clinical Diagnosis of Genomic Imbalance Clin. Chem., December 1, 2007; 53(12): 2051 - 2059. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. H. Kim, S. M. Dhanasekaran, R. Mehra, S. A. Tomlins, W. Gu, J. Yu, C. Kumar-Sinha, X. Cao, A. Dash, L. Wang, et al. Integrative Analysis of Genomic Aberrations Associated with Prostate Cancer Progression Cancer Res., September 1, 2007; 67(17): 8229 - 8239. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Aburatani Copy Number Analysis in Cancer Research Am. Assoc. Cancer Res. Educ. Book, April 14, 2007; 2007(1): 213 - 218. [Full Text] [PDF] |
||||
![]() |
D. A. Scott, M. Klaassens, A. M. Holder, K. P. Lally, C. J. Fernandes, R.-J. Galjaard, D. Tibboel, A. de Klein, and B. Lee Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia Hum. Mol. Genet., February 15, 2007; 16(4): 424 - 430. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Fiegler, R. Redon, D. Andrews, C. Scott, R. Andrews, C. Carder, R. Clark, O. Dovey, P. Ellis, L. Feuk, et al. Accurate and reliable high-throughput detection of copy number variation in the human genome Genome Res., December 1, 2006; 16(12): 1566 - 1574. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. A. Peiffer, J. M. Le, F. J. Steemers, W. Chang, T. Jenniges, F. Garcia, K. Haden, J. Li, C. A. Shaw, J. Belmont, et al. High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping Genome Res., September 1, 2006; 16(9): 1136 - 1148. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. N. van Wieringen, J. A. M. Belien, S. J. Vosse, E. M. Achame, and B. Ylstra ACE-it: a tool for genome-wide integration of gene dosage and RNA expression data Bioinformatics, August 1, 2006; 22(15): 1919 - 1920. [Abstract] [Full Text] [PDF] |
||||








