We have developed methods and identified problems associated with the analy
sis of data generated by high-density, oligonuceotide gene expression array
s. Our methods are aimed at accounting for many of the sources of variation
that make it difficult, at times, to realize consistent results. We presen
t here descriptions of some of these methods and how they impact the analys
is of oligonucleotide gene expression array data. We will discuss the proce
ss of recognizing the "spots" (or features) on the Affymetrix GeneChip(R) p
robe arrays, correcting for background and intensity gradients in the resul
ting images, scaling/normalizing an array to allow array-to-array compariso
ns, monitoring probe performance with respect to hybridization efficiency,
and assessing whether a gene is present or differentially expressed. Exampl
es from the analyses of gene expression validation data are presented to co
ntrast the different methods applied to these types of data, J. Cell. Bioch
em. 80.192-202, 2000. (C) 2000 Wiley-Liss, Inc.