Bioinformatics Vol. 16 no. 8 2000
Pages 685-698
© 2000 Oxford University Press
Original Paper |
Generation of patterns from gene expression data by assigning confidence to differentially expressed genes
1 Center for Bioinformatics, University of
Pennsylvania, Philadelphia, PA 19104, USA
2 Hematology/Oncology Research, A.I. duPont
Hospital for Children, Wilmington, DE 19803, and Department of
Pediatrics, Jefferson Medical College, Philadelphia, PA 19107, USA
3 Division of Hematology, The
Children’s Hospital of Philadelphia and Center for
Bioinformatics, University of Pennsylvania, Philadelphia, PA 19104,
USA
Received on December 15, 1999
; revised on March 14, 2000
; accepted on March 21, 2000
Motivation: A protocol is described to attach expression patterns to genes represented in a collection of hybridization array experiments. Discrete values are used to provide an easily interpretable description of differential expression. Binning cutoffs for each sample type are chosen automatically, depending on the desired false-positive rate for the predictions of differential expression. Confidence levels are derived for the statement that changes in observed levels represent true changes in expression. We have a novel method for calculating this confidence, which gives better results than the standard methods. Our method reflects the broader change of focus in the field from studying a few genes with many replicates to studying many (possibly thousands) of genes simultaneously, but with relatively few replicates. Our approach differs from standard methods in that it exploits the fact that there are many genes on the arrays. These are used to estimate for each sample type an appropriate distribution that is employed to control the false-positive rate of the predictions made. Satisfactory results can be obtained using this method with as few as two replicates.
Results: The method is illustrated through applications to macroarray and microarray datasets. The first is an erythroid development dataset that we have generated using nylon filter arrays. Clones for genes whose expression is known in these cells were assigned expression patterns which are in accordance with what was expected and which are not picked up by the standards methods. Moreover, genes differentially expressed between normal and leukemic cells were identified. These included genes whose expression was altered upon induction of the leukemic cells to differentiate. The second application is to the microarray data by Alizadeh et al. (2000). Our results are in accordance with their major findings and offer confidence measures for the predictions made. They also provide new insights for further analysis.
Availability: Software is available on request from the authors.
Contact: manduchi{at}pcbi.upenn.edu
To whom correspondence should be addressed.
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