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dc.contributor.authorOkoniewski, Michal J
dc.contributor.authorHey, Yvonne
dc.contributor.authorPepper, Stuart D
dc.contributor.authorMiller, Crispin J
dc.date.accessioned2009-06-15T12:19:06Z
dc.date.available2009-06-15T12:19:06Z
dc.date.issued2007-02
dc.identifier.citationHigh correspondence between Affymetrix exon and standard expression arrays. 2007, 42 (2):181-5 BioTechniquesen
dc.identifier.issn0736-6205
dc.identifier.pmid17373482
dc.identifier.urihttp://hdl.handle.net/10541/70474
dc.description.abstractExon arrays aim to provide comprehensive gene expression data at the level of individual exons, similar to that provided on a per-gene basis by existing expression arrays. This report describes the performance of Affymetrix GeneChip Human Exon 1.0 ST array by using replicated RNA samples from two human cell lines, MCF7 and MCF10A, hybridized both to Exon 1.0 ST and to HG-U133 Plus2 arrays. Cross-comparison between array types requires an appropriate mapping to be found between individual probe sets. Three possible mappings were considered, reflecting different strategies for dealing with probe sets that target different parts of the same transcript. Irrespective of the mapping used, Exon 1.0 ST and HG-U133 Plus2 arrays show a high degree of correspondence. More than 80% of HG-U133 Plus2 probe sets may be mapped to the Exon chip, and fold changes are found well preserved for over 96% of those probe sets detected present. Since HG-U133 Plus2 arrays have already been extensively validated, these results lend a significant degree of confidence to exon arrays.
dc.language.isoenen
dc.subject.meshCell Line
dc.subject.meshExons
dc.subject.meshGene Expression
dc.subject.meshHumans
dc.subject.meshMolecular Probes
dc.subject.meshNucleic Acid Hybridization
dc.subject.meshPolymerase Chain Reaction
dc.subject.meshRNA, Messenger
dc.titleHigh correspondence between Affymetrix exon and standard expression arraysen
dc.typeArticleen
dc.contributor.departmentThe Paterson Institute for Cancer Research, The University of Manchester, Christie Hospital Site, Manchester, UK. mokoniewski@picr.man.ac.uken
dc.identifier.journalBioTechniquesen
html.description.abstractExon arrays aim to provide comprehensive gene expression data at the level of individual exons, similar to that provided on a per-gene basis by existing expression arrays. This report describes the performance of Affymetrix GeneChip Human Exon 1.0 ST array by using replicated RNA samples from two human cell lines, MCF7 and MCF10A, hybridized both to Exon 1.0 ST and to HG-U133 Plus2 arrays. Cross-comparison between array types requires an appropriate mapping to be found between individual probe sets. Three possible mappings were considered, reflecting different strategies for dealing with probe sets that target different parts of the same transcript. Irrespective of the mapping used, Exon 1.0 ST and HG-U133 Plus2 arrays show a high degree of correspondence. More than 80% of HG-U133 Plus2 probe sets may be mapped to the Exon chip, and fold changes are found well preserved for over 96% of those probe sets detected present. Since HG-U133 Plus2 arrays have already been extensively validated, these results lend a significant degree of confidence to exon arrays.


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