Evaluation of Normalization Procedures for Oligonucleotide Array Data Based On Spiked cRNA Controls

DSpace/Manakin Repository

Evaluation of Normalization Procedures for Oligonucleotide Array Data Based On Spiked cRNA Controls

Citable link to this page


Title: Evaluation of Normalization Procedures for Oligonucleotide Array Data Based On Spiked cRNA Controls
Author: Brown, Eugene L; Whitley, Maryann Z; Tucker-Kellogg, Greg; Slonim, Donna K; Hill, Andrew A.; Hunter, Craig P.

Note: Order does not necessarily reflect citation order of authors.

Citation: Hill, Andrew A, Eugene L. Brown, Maryann Z. Whitley, Greg Tucker-Kellogg, Craig P. Hunter, and Donna K. Slonim. 2001. Evaluation of normalization procedures for oligonucleotide array data based on spiked cRNA controls. Genome Biology 2(12): research0055.1-research0055.13.
Full Text & Related Files:
Abstract: Background: Affymetrix oligonucleotide arrays simultaneously measure the abundances of thousands of mRNAs in biological samples. Comparability of array results is necessary for the creation of large-scale gene expression databases. The standard strategy for normalizing oligonucleotide array readouts has practical drawbacks. We describe alternative normalization procedures for oligonucleotide arrays based on a common pool of known biotin-labeled cRNAs spiked into each hybridization. Results: We first explore the conditions for validity of the 'constant mean assumption', the key assumption underlying current normalization methods. We introduce 'frequency normalization', a 'spike-in'-based normalization method which estimates array sensitivity, reduces background noise and allows comparison between array designs. This approach does not rely on the constant mean assumption and so can be effective in conditions where standard procedures fail. We also define 'scaled frequency', a hybrid normalization method relying on both spiked transcripts and the constant mean assumption while maintaining all other advantages of frequency normalization. We compare these two procedures to a standard global normalization method using experimental data. We also use simulated data to estimate accuracy and investigate the effects of noise. We find that scaled frequency is as reproducible and accurate as global normalization while offering several practical advantages. Conclusions: Scaled frequency quantitation is a convenient, reproducible technique that performs as well as global normalization on serial experiments with the same array design, while offering several additional features. Specifically, the scaled-frequency method enables the comparison of expression measurements across different array designs, yields estimates of absolute message abundance in cRNA and determines the sensitivity of individual arrays.
Published Version: http://genomebiology.com/2001/2/12/research/0055
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC64840/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4457701
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search