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dc.contributor.author
Sims, Andrew H.
dc.contributor.author
Smethurst, Graeme J.
dc.contributor.author
Hey, Yvonne
dc.contributor.author
Okoniewski, Michal J.
dc.contributor.author
Pepper, Stuart D.
dc.contributor.author
Howell, Anthony
dc.contributor.author
Miller, Crispin J.
dc.contributor.author
Clarke, Robert B.
dc.date.accessioned
2018-12-11T10:14:54Z
dc.date.available
2018-12-11T10:14:54Z
dc.date.issued
2008-09-21
dc.identifier.issn
1755-8794
dc.identifier.other
10.1186/1755-8794-1-42
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/309939
dc.identifier.doi
10.3929/ethz-a-005751409
dc.description.abstract
Background The number of gene expression studies in the public domain is rapidly increasing, representing a highly valuable resource. However, dataset-specific bias precludes meta-analysis at the raw transcript level, even when the RNA is from comparable sources and has been processed on the same microarray platform using similar protocols. Here, we demonstrate, using Affymetrix data, that much of this bias can be removed, allowing multiple datasets to be legitimately combined for meaningful meta-analyses. Results A series of validation datasets comparing breast cancer and normal breast cell lines (MCF7 and MCF10A) were generated to examine the variability between datasets generated using different amounts of starting RNA, alternative protocols, different generations of Affymetrix GeneChip or scanning hardware. We demonstrate that systematic, multiplicative biases are introduced at the RNA, hybridization and image-capture stages of a microarray experiment. Simple batch mean-centering was found to significantly reduce the level of inter-experimental variation, allowing raw transcript levels to be compared across datasets with confidence. By accounting for dataset-specific bias, we were able to assemble the largest gene expression dataset of primary breast tumours to-date (1107), from six previously published studies. Using this meta-dataset, we demonstrate that combining greater numbers of datasets or tumours leads to a greater overlap in differentially expressed genes and more accurate prognostic predictions. However, this is highly dependent upon the composition of the datasets and patient characteristics. Conclusion Multiplicative, systematic biases are introduced at many stages of microarray experiments. When these are reconciled, raw data can be directly integrated from different gene expression datasets leading to new biological findings with increased statistical power.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
BioMed Central
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/2.0/
dc.subject
Validation dataset
en_US
dc.subject
Gene expression dataset
en_US
dc.subject
Luminal tumour
en_US
dc.subject
Gene expression classifier
en_US
dc.subject
Supervise principal component analysis
en_US
dc.title
The removal of multiplicative, systematic bias allows integration of breast cancer gene expression datasets – improving meta-analysis and prediction of prognosis
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 2.0 Generic
ethz.journal.title
BMC Medical Genomics
ethz.journal.volume
1
en_US
ethz.journal.issue
42
ethz.journal.abbreviated
BMC med. genomics
ethz.pages.start
42
en_US
ethz.size
14 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.code.ddc
DDC - DDC::5 - Science::570 - Life sciences
en_US
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
en_US
ethz.date.deposited
2017-06-08T21:26:25Z
ethz.source
ECOL
ethz.source
ECIT
ethz.identifier.importid
imp59366acd53ae669901
ethz.identifier.importid
imp59364c4198cfc25514
ethz.ecolpid
eth:41368
ethz.ecitpid
pub:26247
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2018-12-11T10:15:33Z
ethz.rosetta.lastUpdated
2024-02-02T06:48:27Z
ethz.rosetta.versionExported
true
dc.identifier.olduri
http://hdl.handle.net/20.500.11850/150951
dc.identifier.olduri
http://hdl.handle.net/20.500.11850/14594
ethz.COinS
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