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Washing scaling of GeneChip microarray expression

dc.contributor.authorBinder, Hans
dc.contributor.authorKrohn, Knut
dc.contributor.authorBurden, Conrad J
dc.date.accessioned2016-01-15T00:10:24Z
dc.date.available2016-01-15T00:10:24Z
dc.date.issued2010-05-28
dc.date.updated2016-02-24T08:23:48Z
dc.description.abstractBACKGROUND Post-hybridization washing is an essential part of microarray experiments. Both the quality of the experimental washing protocol and adequate consideration of washing in intensity calibration ultimately affect the quality of the expression estimates extracted from the microarray intensities. RESULTS We conducted experiments on GeneChip microarrays with altered protocols for washing, scanning and staining to study the probe-level intensity changes as a function of the number of washing cycles. For calibration and analysis of the intensity data we make use of the 'hook' method which allows intensity contributions due to non-specific and specific hybridization of perfect match (PM) and mismatch (MM) probes to be disentangled in a sequence specific manner. On average, washing according to the standard protocol removes about 90% of the non-specific background and about 30-50% and less than 10% of the specific targets from the MM and PM, respectively. Analysis of the washing kinetics shows that the signal-to-noise ratio doubles roughly every ten stringent washing cycles. Washing can be characterized by time-dependent rate constants which reflect the heterogeneous character of target binding to microarray probes. We propose an empirical washing function which estimates the survival of probe bound targets. It depends on the intensity contribution due to specific and non-specific hybridization per probe which can be estimated for each probe using existing methods. The washing function allows probe intensities to be calibrated for the effect of washing. On a relative scale, proper calibration for washing markedly increases expression measures, especially in the limit of small and large values. CONCLUSIONS Washing is among the factors which potentially distort expression measures. The proposed first-order correction method allows direct implementation in existing calibration algorithms for microarray data. We provide an experimental 'washing data set' which might be used by the community for developing amendments of the washing correction.
dc.description.sponsorshipThis publication is supported by the Leipzig Interdisciplinary Research Cluster of Genetic Factors, Clinical Phenotypes and Environment (LIFE Center, Universität Leipzig) and an Australian Academy of Science Visits to Europe grant. LIFE is funded by means of the European Union, by the European Regional Development Fund (ERFD) and by means of the Free State of Saxony within the framework of the excellence initiative.en_AU
dc.identifier.issn1471-2105en_AU
dc.identifier.urihttp://hdl.handle.net/1885/95413
dc.publisherBioMed Central
dc.rights© Binder et al. 2010 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceBMC Bioinformatics
dc.subjectgene expression profiling
dc.subjectkinetics
dc.subjectnucleic acid hybridization
dc.subjectoligonucleotide array sequence analysis
dc.subjectalgorithms
dc.titleWashing scaling of GeneChip microarray expression
dc.typeJournal article
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage291en_AU
local.contributor.affiliationBinder, Hans, University Leipzig, Germanyen_AU
local.contributor.affiliationKrohn, Knut, University Leipzig, Germanyen_AU
local.contributor.affiliationBurden, Conrad, College of Physical and Mathematical Sciences, CPMS Mathematical Sciences Institute, Centre for Mathematics and Its Applications, The Australian National Universityen_AU
local.contributor.authoruidu1571037en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor010402en_AU
local.identifier.ariespublicationf2965xPUB224en_AU
local.identifier.citationvolume11en_AU
local.identifier.doi10.1186/1471-2105-11-291en_AU
local.identifier.essn1471-2105en_AU
local.identifier.scopusID2-s2.0-77952701692
local.identifier.thomsonID000279733800001
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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