Empirical Bayes models for multiple probe type microarrays at the probe level
Artikel i vetenskaplig tidskrift, 2008

Background: When analyzing microarray data a primary objective is often to find differentially expressed genes. With empirical Bayes and penalized t-tests the sample variances are adjusted towards a global estimate, producing more stable results compared to ordinary t-tests. However, for Affymetrix type data a clear dependency between variability and intensity-level generally exists, even for logged intensities, most clearly for data at the probe level but also for probe-set summarizes such as the MAS5 expression index. As a consequence, adjustment towards a global estimate results in an intensity-level dependent false positive rate. Results: We propose two new methods for finding differentially expressed genes, Probe level Locally moderated Weighted median-t (PLW) and Locally Moderated Weighted-t (LMW). Both methods use an empirical Bayes model taking the dependency between variability and intensity-level into account. A global covariance matrix is also used allowing for differing variances between arrays as well as array-to-array correlations. PLW is specially designed for Affymetrix type arrays (or other multiple-probe arrays). Instead of making inference on probe-set summaries, comparisons are made separately for each perfect-match probe and are then summarized into one score for the probe-set. Conclusion: The proposed methods are compared to 14 existing methods using five spike-in data sets. For RMA and GCRMA processed data, PLW has the most accurate ranking of regulated genes in four out of the five data sets, and LMW consistently performs better than all examined moderated t-tests when used on RMA, GCRMA, and MAS5 expression indexes. © 2008 Åstrand et al; licensee BioMed Central Ltd.



oligonucleotide arrays


differential gene-expression



Göteborgs universitet

Chalmers, Matematiska vetenskaper

Petter Mostad

Chalmers, Matematiska vetenskaper, matematisk statistik

Göteborgs universitet

Mats Rudemo

Göteborgs universitet

Chalmers, Matematiska vetenskaper, matematisk statistik

BMC Bioinformatics

1471-2105 (ISSN)

Vol. 9 156


Sannolikhetsteori och statistik