Title |
The pitfalls of platform comparison: DNA copy number array technologies assessed
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Published in |
BMC Genomics, December 2009
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DOI | 10.1186/1471-2164-10-588 |
Pubmed ID | |
Authors |
Christina Curtis, Andy G Lynch, Mark J Dunning, Inmaculada Spiteri, John C Marioni, James Hadfield, Suet-Feung Chin, James D Brenton, Simon Tavaré, Carlos Caldas |
Abstract |
The accurate and high resolution mapping of DNA copy number aberrations has become an important tool by which to gain insight into the mechanisms of tumourigenesis. There are various commercially available platforms for such studies, but there remains no general consensus as to the optimal platform. There have been several previous platform comparison studies, but they have either described older technologies, used less-complex samples, or have not addressed the issue of the inherent biases in such comparisons. Here we describe a systematic comparison of data from four leading microarray technologies (the Affymetrix Genome-wide SNP 5.0 array, Agilent High-Density CGH Human 244A array, Illumina HumanCNV370-Duo DNA Analysis BeadChip, and the Nimblegen 385 K oligonucleotide array). We compare samples derived from primary breast tumours and their corresponding matched normals, well-established cancer cell lines, and HapMap individuals. By careful consideration and avoidance of potential sources of bias, we aim to provide a fair assessment of platform performance. |
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Geographical breakdown
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United States | 3 | 2% |
Canada | 2 | 1% |
Belgium | 2 | 1% |
Mexico | 1 | <1% |
Finland | 1 | <1% |
Russia | 1 | <1% |
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Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 52 | 39% |
Student > Ph. D. Student | 32 | 24% |
Student > Master | 13 | 10% |
Professor > Associate Professor | 12 | 9% |
Other | 5 | 4% |
Other | 14 | 10% |
Unknown | 6 | 4% |
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Mathematics | 3 | 2% |
Other | 10 | 7% |
Unknown | 10 | 7% |