Comparison of array-based comparative genomic hybridization with gene expression-based regional expression biases to identify genetic abnormalities in hepatocellular carcinoma.docVIP
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Comparison of array-based comparative genomic hybridization with gene expression-based regional expression biases to identify genetic abnormalities in hepatocellular carcinoma
BMC Genomics
BioMedCentral
Methodology article
Open Access
Comparison of array-based comparative genomic hybridization
with gene expression-based regional expression biases to identify
genetic abnormalities in hepatocellular carcinoma
Kyle A Furge*1, Karl J Dykema1, Coral Ho2 and Xin Chen2,3,4
Address: 1Bioinformatics Special Program, Van Andel Research Institute, 333 Bostwick Ave. NE, Grand Rapids, MI 49503, USA, 2Dept of
Pharmaceutical Sciences, University of California, S816 513 Parnassus Ave., San Francisco, CA 94143-0046, USA, 3Cancer Center, University of
California, S816 513 Parnassus Ave., San Francisco, CA 94143-0046, USA and 4Liver Center, University of California, S816 513 Parnassus Ave.,
San Francisco, CA 94143-0046, USA
Email: Kyle A Furge* - kyle.furge@; Karl J Dykema - karl.dykema@; Coral Ho - coralho@;
Xin Chen - xinchen@
* Corresponding author
Published: 09 May 2005
Received: 10 January 2005
Accepted: 09 May 2005
BMC Genomics 2005, 6:67
doi:10.1186/1471-2164-6-67
This article is available from: /1471-2164/6/67
? 2005 Furge et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background: Regional expression biases (REBs) are genetic intervals where gene expression is
coordinately changed. For example, if a region of the genome is amplified, often the majority of
genes that map within the amplified region show increased expression when compared to genes
located in cytogenetically normal regions. As such, REBs have the potential to act as surrogates for
cytogenetic data traditionally obtained using molecular technologies such as comparative genomic
hybridization. However as REBs are identified using transcriptional information, detection of REBs
may also identify local tran
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