Skip NavigationSkip to Content

Three microarray platforms: an analysis of their concordance in profiling gene expression

  1. Author:
    Petersen, D.
    Chandramouli, G. V. R.
    Geoghegan, J.
    Hilburn, J.
    Paarlberg, J.
    Kim, C. H.
    Munroe, D.
    Gangi, L.
    Han, J.
    Puri, R.
    Staudt, L.
    Weinstein, J.
    Barrett, J. C.
    Green, J.
    Kawasaki, E. S.
  2. Author Address

    NCI, Ctr Adv Technol, Canc Res Ctr, Gaithersburg, MD 20877 USA. SAIC Frederick, Lab Mol Technol, Frederick, MD 21701 USA. US FDA, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA. NCI, Canc Res Ctr, Bethesda, MD 20892 USA Kawasaki, ES, NCI, Ctr Adv Technol, Canc Res Ctr, Gaithersburg, MD 20877 USA
    1. Year: 2005
    2. Date: MAY 5
  1. Journal: Bmc Genomics
    1. 6
    2. Art. No. 63
  2. Type of Article: Article
  1. Abstract:

    Background: Microarrays for the analysis of gene expression are of three different types: short oligonucleotide (25-30 base), long oligonucleotide (50-80 base), and cDNA ( highly variable in length). The short oligonucleotide and cDNA arrays have been the mainstay of expression analysis to date, but long oligonucleotide platforms are gaining in popularity and will probably replace cDNA arrays. As part of a validation study for the long oligonucleotide arrays, we compared and contrasted expression profiles from the three formats, testing RNA from six different cell lines against a universal reference standard.Results: The three platforms had 6430 genes in common. In general, correlation of gene expression levels across the platforms was good when defined by concordance in the direction of expression difference (upregulation or downregulation), scatter plot analysis, principal component analysis, cell line correlation or quantitative RT-PCR. The overall correlations (r values) between platforms were in the range 0.7 to 0.8, as determined by analysis of scatter plots. When concordance was measured for expression ratios significant at p-values of < 0.05 and at expression threshold levels of 1.5 and 2-fold, the agreement among the platforms was very high, ranging from 93% to 100%.Conclusion: Our results indicate that the long oligonucleotide platform is highly suitable for expression analysis and compares favorably with the cDNA and short oligonucleotide varieties. All three platforms can give similar and reproducible results if the criterion is the direction of change in gene expression and minimal emphasis is placed on the magnitude of change

    See More

External Sources

  1. WOS: 000229379600001

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel