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dc.contributor.authorAntipova, Alena A.
dc.contributor.authorTamayo, Pablo
dc.contributor.authorGolub, Todd R.
dc.date.accessioned2010-10-12T14:09:51Z
dc.date.available2010-10-12T14:09:51Z
dc.date.issued2002-11
dc.date.submitted2002-09
dc.identifier.issn1465-6906
dc.identifier.urihttp://hdl.handle.net/1721.1/59013
dc.description.abstractBackground: One of the factors limiting the number of genes that can be analyzed on high-density oligonucleotide arrays is that each transcript is probed by multiple oligonucleotide probes. To reduce the number of probes required for each gene, a systematic approach to choosing the most representative probes is needed. A method is presented for reducing the number of probes per gene while maximizing the fidelity to the original array design. Results: The methodology has been tested on a dataset comprising 317 Affymetrix HuGeneFL GeneChips. The performance of the original and reduced probe sets was compared in four cancer-classification problems. The results of these comparisons show that reduction of the probe set by 95% does not dramatically affect performance, and thus illustrate the feasibility of substantially reducing probe numbers without significantly compromising sensitivity and specificity of detection. Conclusions: The strategy described here is potentially useful for designing small, limited-probe genome-wide arrays for screening applications.en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/gb-2002-3-12-research0073en_US
dc.rightsCreative Commons Attributionen_US
dc.sourceBioMed Central Ltden_US
dc.titleA strategy for oligonucleotide microarray probe reductionen_US
dc.typeArticleen_US
dc.identifier.citationGenome Biology. 2002 Nov 25;3(12):research0073-research0073.4en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorAntipova, Alena A.
dc.contributor.mitauthorTamayo, Pablo
dc.contributor.mitauthorGolub, Todd R.
dc.relation.journalGenome Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.identifier.pmid12537562
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:07:02Z
dc.language.rfc3066en
dc.rights.holderAntipova et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsAntipova, Alena A; Tamayo, Pablo; Golub, Todd Ren
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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