{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,10]],"date-time":"2026-03-10T11:29:50Z","timestamp":1773142190023,"version":"3.50.1"},"reference-count":12,"publisher":"Oxford University Press (OUP)","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2005,4,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Motivation: An important underlying assumption of any experiment is that the experimental subjects are similar across levels of the treatment variable, so that changes in the response variable can be attributed to exposure to the treatment under study. This assumption is often not valid in the analysis of a microarray experiment due to systematic biases in the measured expression levels related to experimental factors such as spot location (often referred to as a print-tip effect), arrays, dyes, and various interactions of these effects. Thus, normalization is a critical initial step in the analysis of a microarray experiment, where the objective is to balance the individual signal intensity levels across the experimental factors, while maintaining the effect due to the treatment under investigation.<\/jats:p>\n               <jats:p>Results: Various normalization strategies have been developed including log-median centering, analysis of variance modeling, and local regression smoothing methods for removing linear and\/or intensity-dependent systematic effects in two-channel microarray experiments. We describe a method that incorporates many of these into a single strategy, referred to as two-channel fastlo, and is derived from a normalization procedure that was developed for single-channel arrays. The proposed normalization procedure is applied to a two-channel dose\u2013response experiment.<\/jats:p>\n               <jats:p>Availability: The SAS macro for two-channel fastlo is available from the authors upon request and the data used to test the methods is publicly available at http:\/\/www.bch.msu.edu\/~zacharet\/publications\/supplementary\/ee_dr<\/jats:p>\n               <jats:p>Contact: \u00a0eckel@mayo.edu<\/jats:p>","DOI":"10.1093\/bioinformatics\/bti105","type":"journal-article","created":{"date-parts":[[2004,10,29]],"date-time":"2004-10-29T00:51:45Z","timestamp":1099011105000},"page":"1078-1083","source":"Crossref","is-referenced-by-count":61,"title":["Normalization of two-channel microarray experiments: a semiparametric approach"],"prefix":"10.1093","volume":"21","author":[{"given":"J. E.","family":"Eckel","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Gennings","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T. M.","family":"Therneau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L. D.","family":"Burgoon","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D. R.","family":"Boverhof","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T. R.","family":"Zacharewski","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2004,10,28]]},"reference":[{"key":"2023013107271440500_B1","doi-asserted-by":"crossref","unstructured":"Ballman, K.V., Grill, D.E., Oberg, A.L., Therneau, T.M. 2004Faster cyclic loess: normalizing DNA arrays via linear models. Bioinformatics202778\u20132786","DOI":"10.1093\/bioinformatics\/bth327"},{"key":"2023013107271440500_B2","unstructured":"Bolstad, B.M., Arizarr, R.A., Astrand, M., Speed, T.P. 2003A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics19185\u2013193"},{"key":"2023013107271440500_B3","unstructured":"Dudoit, S., Yang, Y.H., Callow, M.J., Speed, T.P. 2002Statistical methods for identifying differentially expressed genes in replicated cDNA microarray experiments. 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