Nature Biotechnology
- 24, 1123 - 1131 (2006)
Published online: 8 September 2006; | doi:10.1038/nbt1241
Using RNA sample titrations to assess microarray platform performance and normalization techniquesRichard Shippy, Stephanie Fulmer-Smentek, Roderick V Jensen, Wendell D Jones, Paul K Wolber, Charles D Johnson, P Scott Pine, Cecilie Boysen, Xu Guo, Eugene Chudin, Yongming Andrew Sun, James C Willey, Jean Thierry-Mieg, Danielle Thierry-Mieg, Robert A Setterquist, Mike Wilson, Anne Bergstrom Lucas, Natalia Novoradovskaya, Adam Papallo, Yaron Turpaz, Shawn C Baker, Janet A Warrington, Leming Shi & Damir Herman Supplementary Fig. 1 (doc 775K) Linear regression fitting of Ci/Bi vs. Ai/Bi for each platform, normalization method and site to estimate the true mixture coefficients c, c for the C sample from the data. Supplementary Fig. 2 (doc 60K) Illustration providing a possible explanation for the asymmetry (i.e., median A>B ( C) medianA<B ( C) and median A>B ( D) medianA<B ( D)) in the box plots on either side of Figure 4 (particularly the differences in median values). Supplementary Fig. 3 (doc 60K) Percentage of genes achieving the specified level of apparent power between the RNA titration mixtures and independent samples. Supplementary Fig. 4 (doc 430K) Impact of different normalization methods on signal CVs for each microarray platform separated by site and sample. Supplementary Fig. 5 (doc 45K) Derivation of formulas within Box 1 to clarify calculations for mRNA fractions. Supplementary Table 1 (doc 45K) Gene counts for each commercial whole genome microarray platform separated by site.
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