Abstract
Background Currently, two main technologies are used for screening of
DNA copy number; the BAC (Bacterial Artificial Chromosome) and the recently
developed oligonucleotide-based CGH (Chromosomal Comparative Genomic
Hybridization) arrays which are capable of detecting small genomic regions
with amplification or deletion. The correlation as well as the discriminative
power of these platforms has never been compared statistically on a
significant set of human patient samples. Results In this paper, we present
an exhaustive comparison between the two CGH platforms, undertaken at two
independent sites using the same batch of DNA from 19 advanced prostate
cancers. The comparison was performed directly on the raw data and a
significant correlation was found between the two platforms. The correlation
was greatly improved when the data were averaged over large chromosomic
regions using a segmentation algorithm. In addition, this analysis has enabled
the development of a statistical model to discriminate BAC outliers that
might indicate microevents. These microevents were validated by the oligo
platform results. Conclusions This article presents a genome-wide
statistical validation of the oligo array platform on a large set of patient
samples and demonstrates statistically its superiority over the BAC platform
for the identification of chromosomic events. Taking advantage of a large set
of human samples treated by the two technologies, a statistical model has been
developed to show that the BAC platform could also detect microevents.
Original language | English |
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Number of pages | 10 |
Journal | BMC Genomics |
Volume | 8 |
Issue number | 84 |
DOIs | |
Publication status | Published - 2007 |
MoE publication type | A1 Journal article-refereed |