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Differences in gene expression between B-cell chronic lymphocytic leukemia and normal B cells: A meta-analysis of three microarray studies

  • J. Wang
    ,
  • ,
  • W. E. Highsmith
    ,
  • M. J. Keating
    ,
  • L. V. Abruzzo(corresponding author)
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
    ,
  • Mayo Clinic Rochester, MN
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Motivation: A major focus of current cancer research is to identify genes that can be used as markers for prognosis and diagnosis, and as targets for therapy. Microarray technology has been applied extensively for this purpose, even though it has been reported that the agreement between microarray platforms is poor. A critical question is: how can we best combine the measurements of matched genes across microarray platforms to develop diagnostic and prognostic tools related to the underlying biology? Results: We introduce a statistical approach within a Bayesian framework to combine the microarray data on matched genes from three investigations of gene expression profiling of B-cell chronic lymphocytic leukemia (CLL) and normal B cells (NBC) using three different microarray platforms, oligonucleotide arrays, cDNA arrays printed on glass slides and cDNA arrays printed on nylon membranes. Using this approach, we identified a number of genes that were consistently differentially expressed between CLL and NBC samples.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 3166-3178 (13 pages)

Journal (Volume, Issue Number)

Bioinformatics (Volume 20, Issue 17)

Publication milestones

  • Published - 11/22/2004

Publication status

Published - 11/22/2004

ISSN

1367-4803

Publication IDs

  • Scopus: 10244224128
  • PubMed: 15231529

Publication metrics

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Scopus
citations
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1
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Fractional count
4
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0.80
Fractional count
1
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1

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111
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Funding Details

The authors thank Ms Tammy Krogmann and Ms Lynn Barron for expert technical assistance. This work is supported in part by the State of Texas under ARP/ATP grant 003657-0020-2001.
FundersFunding number
ATP
003657-0020-2001
Texas State University
-
ARP
-