Washing scaling of GeneChip microarray expression

<p>Abstract</p> <p>Background</p> <p>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 expr...

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Main Authors: Krohn Knut, Binder Hans, Burden Conrad J
Format: Article
Language:English
Published: BMC 2010-05-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/11/291
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spelling doaj-1475b61480864dd4a9bf44238fd467932020-11-24T21:46:01ZengBMCBMC Bioinformatics1471-21052010-05-0111129110.1186/1471-2105-11-291Washing scaling of GeneChip microarray expressionKrohn KnutBinder HansBurden Conrad J<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p> http://www.biomedcentral.com/1471-2105/11/291
collection DOAJ
language English
format Article
sources DOAJ
author Krohn Knut
Binder Hans
Burden Conrad J
spellingShingle Krohn Knut
Binder Hans
Burden Conrad J
Washing scaling of GeneChip microarray expression
BMC Bioinformatics
author_facet Krohn Knut
Binder Hans
Burden Conrad J
author_sort Krohn Knut
title Washing scaling of GeneChip microarray expression
title_short Washing scaling of GeneChip microarray expression
title_full Washing scaling of GeneChip microarray expression
title_fullStr Washing scaling of GeneChip microarray expression
title_full_unstemmed Washing scaling of GeneChip microarray expression
title_sort washing scaling of genechip microarray expression
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2010-05-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
url http://www.biomedcentral.com/1471-2105/11/291
work_keys_str_mv AT krohnknut washingscalingofgenechipmicroarrayexpression
AT binderhans washingscalingofgenechipmicroarrayexpression
AT burdenconradj washingscalingofgenechipmicroarrayexpression
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