Author:
Barczak Andrea,Rodriguez Madeleine Willkom,Hanspers Kristina,Koth Laura L.,Tai Yu Chuan,Bolstad Benjamin M.,Speed Terence P.,Erle David J.
Abstract
DNA microarrays produced by deposition (or `spotting')of a single long
oligonucleotide probe for each gene may be an attractive alternative to other
types of arrays. We produced spotted oligonucleotide arrays using two large
collections of ∼70-mer probes, and used these arrays to analyze gene
expression in two dissimilar human RNA samples. These samples were also
analyzed using arrays produced by in situ synthesis of sets of multiple short
(25-mer)oligonucleotides for each gene (Affymetrix GeneChips). We compared
expression measurements for 7344 genes that were represented in both long
oligonucleotide probe collections and the in situ-synthesized 25-mer arrays.
We found strong correlations (r = 0.8–0.9)between relative gene
expression measurements made with spotted long oligonucleotide probes and in
situ-synthesized 25-mer probe sets. Spotted long oligonucleotide arrays were
suitable for use with both unamplified cDNA and amplified RNA targets, and are
a cost-effective alternative for many functional genomics applications. Most
previously reported evaluations of microarray technologies have focused on
expression measurements made on a relatively small number of genes. The
approach described here involves far more gene expression measurements and
provides a useful method for comparing existing and emerging techniques for
genome-scale expression analysis.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics (clinical),Genetics
Cited by
142 articles.
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