AI Article Synopsis

  • The paper evaluates various signal quantification methods and statistical tests for finding differential expression in Affymetrix microarray data.
  • The study used two datasets: a Latin Square spike-in dataset and rat liver transcriptomics data from drug treatments.
  • The authors recommend using GCRMA for signal quantification, with Cyber-T or SAM for differential expression detection, noting that MAS5 was less effective compared to other methods.

Article Abstract

Signal quantification and detection of differential expression are critical steps in the analysis of Affymetrix microarray data. Many methods have been proposed in the literature for each of these steps. The goal of this paper is to evaluate several signal quantification methods (GCRMA, RSVD, VSN, MAS5, and Resolver) and statistical methods for differential expression (t test, Cyber-T, SAM, LPE, RankProducts, Resolver RatioBuild). Our particular focus is on the ability to detect differential expression via statistical tests. We have used two different datasets for our evaluation. First, we have used the HG-U133 Latin Square spike in dataset developed by Affymetrix. Second, we have used data from an in-house rat liver transcriptomics study following 30 different drug treatments generated using the Affymetrix RAE230A chip. Our overall recommendation based on this study is to use GCRMA for signal quantification. For detection of differential expression, GCRMA coupled with Cyber-T or SAM is the best approach, as measured by area under the receiver operating characteristic (ROC) curve. The integrated pipeline in Resolver RatioBuild combining signal quantification and detection of differential expression is an equally good alternative for detecting differentially expressed genes. For most of the differential expression algorithms we considered, the performance using MAS5 signal quantification was inferior to that of the other methods we evaluated.

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Source
http://dx.doi.org/10.1089/omi.2006.10.555DOI Listing

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