Gene selection with multiple ordering criteria
<p>Abstract</p> <p>Background</p> <p>A microarray study may select different differentially expressed gene sets because of different selection criteria. For example, the fold-change and p-value are two commonly known criteria to select differentially expressed genes und...
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doaj-51fe9aab69f841a4802ff51c90a6e0172020-11-25T00:24:47ZengBMCBMC Bioinformatics1471-21052007-03-01817410.1186/1471-2105-8-74Gene selection with multiple ordering criteriaTzeng ShengLiTsai Chen-AnChen James JChen Chun-Houh<p>Abstract</p> <p>Background</p> <p>A microarray study may select different differentially expressed gene sets because of different selection criteria. For example, the fold-change and p-value are two commonly known criteria to select differentially expressed genes under two experimental conditions. These two selection criteria often result in incompatible selected gene sets. Also, in a two-factor, say, treatment by time experiment, the investigator may be interested in one gene list that responds to both treatment and time effects.</p> <p>Results</p> <p>We propose three layer ranking algorithms, point-admissible, line-admissible (convex), and Pareto, to provide a preference gene list from multiple gene lists generated by different ranking criteria. Using the public colon data as an example, the layer ranking algorithms are applied to the three univariate ranking criteria, fold-change, p-value, and frequency of selections by the SVM-RFE classifier. A simulation experiment shows that for experiments with small or moderate sample sizes (less than 20 per group) and detecting a 4-fold change or less, the two-dimensional (p-value and fold-change) convex layer ranking selects differentially expressed genes with generally lower FDR and higher power than the standard p-value ranking. Three applications are presented. The first application illustrates a use of the layer rankings to potentially improve predictive accuracy. The second application illustrates an application to a two-factor experiment involving two dose levels and two time points. The layer rankings are applied to selecting differentially expressed genes relating to the dose and time effects. In the third application, the layer rankings are applied to a benchmark data set consisting of three dilution concentrations to provide a ranking system from a long list of differentially expressed genes generated from the three dilution concentrations.</p> <p>Conclusion</p> <p>The layer ranking algorithms are useful to help investigators in selecting the most promising genes from multiple gene lists generated by different filter, normalization, or analysis methods for various objectives.</p> http://www.biomedcentral.com/1471-2105/8/74 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tzeng ShengLi Tsai Chen-An Chen James J Chen Chun-Houh |
spellingShingle |
Tzeng ShengLi Tsai Chen-An Chen James J Chen Chun-Houh Gene selection with multiple ordering criteria BMC Bioinformatics |
author_facet |
Tzeng ShengLi Tsai Chen-An Chen James J Chen Chun-Houh |
author_sort |
Tzeng ShengLi |
title |
Gene selection with multiple ordering criteria |
title_short |
Gene selection with multiple ordering criteria |
title_full |
Gene selection with multiple ordering criteria |
title_fullStr |
Gene selection with multiple ordering criteria |
title_full_unstemmed |
Gene selection with multiple ordering criteria |
title_sort |
gene selection with multiple ordering criteria |
publisher |
BMC |
series |
BMC Bioinformatics |
issn |
1471-2105 |
publishDate |
2007-03-01 |
description |
<p>Abstract</p> <p>Background</p> <p>A microarray study may select different differentially expressed gene sets because of different selection criteria. For example, the fold-change and p-value are two commonly known criteria to select differentially expressed genes under two experimental conditions. These two selection criteria often result in incompatible selected gene sets. Also, in a two-factor, say, treatment by time experiment, the investigator may be interested in one gene list that responds to both treatment and time effects.</p> <p>Results</p> <p>We propose three layer ranking algorithms, point-admissible, line-admissible (convex), and Pareto, to provide a preference gene list from multiple gene lists generated by different ranking criteria. Using the public colon data as an example, the layer ranking algorithms are applied to the three univariate ranking criteria, fold-change, p-value, and frequency of selections by the SVM-RFE classifier. A simulation experiment shows that for experiments with small or moderate sample sizes (less than 20 per group) and detecting a 4-fold change or less, the two-dimensional (p-value and fold-change) convex layer ranking selects differentially expressed genes with generally lower FDR and higher power than the standard p-value ranking. Three applications are presented. The first application illustrates a use of the layer rankings to potentially improve predictive accuracy. The second application illustrates an application to a two-factor experiment involving two dose levels and two time points. The layer rankings are applied to selecting differentially expressed genes relating to the dose and time effects. In the third application, the layer rankings are applied to a benchmark data set consisting of three dilution concentrations to provide a ranking system from a long list of differentially expressed genes generated from the three dilution concentrations.</p> <p>Conclusion</p> <p>The layer ranking algorithms are useful to help investigators in selecting the most promising genes from multiple gene lists generated by different filter, normalization, or analysis methods for various objectives.</p> |
url |
http://www.biomedcentral.com/1471-2105/8/74 |
work_keys_str_mv |
AT tzengshengli geneselectionwithmultipleorderingcriteria AT tsaichenan geneselectionwithmultipleorderingcriteria AT chenjamesj geneselectionwithmultipleorderingcriteria AT chenchunhouh geneselectionwithmultipleorderingcriteria |
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