Gene Ontology Term Analysis

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The Gene Ontology project describes genes (gene products) using terms from three structured vocabularies: biological process, cellular component and molecular function.

A number of analysis methods in geWorkbench produce a list of interesting genes, for example, those differentially expressed (t-test, ANOVA), or those which show similarities in expression (Hierarchical Clustering, SOM, ARACNe). The Gene Ontology Enrichment component, also referred to as the "GO Terms" component, allows the genes in any such "changed-gene" list to be characterized using the Gene Ontology terms annotated to them. It asks, whether for any particular GO term, the fraction of genes assigned to it in the "changed-gene" list is higher than expected by chance (is over-represented), relative to the fraction of genes assigned to that term in the reference set. In statistical terms, the analysis tests the null hypothesis that, for any particular ontology term, there is no difference in the proportion of genes annotated to it in the reference list and the proportion annotated to it in the test list. The reference list is typically comprised of all genes on a microarray (after any filtering and removal of redundant entries).

The Gene Ontology (GO Terms) analysis component in geWorkbench is built around the Ontologizer 2.0 software product from Peter Robinson's group at the Charite Medical Institute of the Humboldt University in Berlin. It provides several methods for over-representation analysis, including Term-for-Term, Parent-Child, and Topology. More information about these methods can be found at the Ontologizer website at, and in the descriptions and references below.

The Gene Ontology is structured as a directed acyclic graph (DAG). This has several consequences. A term can have more than one parent, and hence there can be multiple paths from the root by which a term can be reached. The Ontologizer code uses the "true path" property of the Gene Ontology in counting genes assigned to a term, by which a gene annotated to any term is considered also annotated to all that term’s parent terms. A term may thus show significant over-representation through the cumulative effects of its children rather than through genes assigned directly to it.

Analysis Component GUI



GeneOntology Analysis Selection.png

Reference Gene List

The first pulldown allows one to choose from the following sources for the reference gene list:

  • All Genes - uses all markers in the current microarray dataset.
  • From Set - if chosen, the second pull-down shows the available sets defined in the Markers component.
  • From File - if chosen, the "Load" button becomes active.

Load - If From File is chosen, the user can load a comma-separated list of markers to use as the reference set.

Text field - displays the contents of the currently loaded reference gene list, regardless of source.

Changed Gene List

The first pull-down allows one to choose from the following sources for the changed-gene list:

  • From Set - if chosen, the second pull-down shows the available sets defined in the Markers component.
  • From File - if chosen, the "Load" button becomes active.
  • From Result Node - if chosen, the second pull-down shows a list of available differential expression (t-test, ANOVA) result nodes from the Project Folders component.

Load - If From File is chosen, the user can load a comma-separated list of markers to use as the changed gene list.

Text field - displays the contents of the currently loaded changed-gene list, except if "From Result Node" is chosen.

Ontology Selection

Not currently implemented, this is intended to allow the loading of alternate ontologies besides the three comprising the Gene Ontology.


GeneOntology Analysis Ontologizer2.png


  • Use loaded annotations - If an annotation file was read in when the microarray dataset was loaded, it is displayed here.
  • Use alternate annotation file - A new or alternate annotation file can be read in by selecting this option. Currently only the Affymetrix annotation file format is supported.
  • Alternate annotation text field - if an alternate annotation file is chosen, the file name will be display in this field.
  • Browse - this button brings up a file browser for choosing an annotation file.

Enrichment Method

GeneOntology Analysis EnrichmentMethod.png

Multiple Testing Correction

GeneOntology Analysis MultipleTesting.png

  • Benjamini-Hochberg -
  • Benjamini-Yekutieli -
  • Bonferroni -
  • Bonferroni-Holm -
  • None (default) -
  • Westfall-Young-Single-Step -
  • Westfall-Young-Step-Down -


Running a GO Terms analysis requires a list of genes to analyze (the study set). Here, we will run a simple t-test on two classes of cell-lines in the BCell-100.exp dataset.

  1. Load Bcell-100.exp
  2. Threshold normalizer: min threshold 1.0.
  3. Log2 Normalize
  4. In Arrays, select the "Class" list of array sets and activate GC B-cell and GC-Tumor (Case).
  5. Run t-test with alpha threshold = 0.01 and using Bonferroni correction.

A new Marker set is created called "Significant Genes" with 437 markers. GeneOntology Analysis Setup.png


  • Alexa A, Rahnenführer J, Lengauer T (2006). Improved scoring of functional groups from gene expression data by decorrelating GO graph structure. Bioinformatics 22(13), pps. 2600-1607 (link to paper)
  • Bauer S, Grossmann S, Vingron M, Robinson PN (2008). Ontologizer 2.0--a multifunctional tool for GO term enrichment analysis and data exploration. Bioinformatics 24(14), pps. 1650-1. (link to paper)
  • Falcon S, Gentleman R. (2007) Using GOstats to test gene lists for GO term association. Bioinformatics 23(2), pps. 257-8. (link to paper)
  • Grossmann S, Bauer S, Robinson PN, Vingron M (2007). Improved detection of overrepresentation of Gene-Ontology annotations with parent child analysis. Bioinformatics 23(22), pps. 3024-31. (link to paper)
  • Robinson PN, Wollstein A, Böhme U, Beattie B. (2004) Ontologizing gene-expression microarray data: characterizing clusters with Gene Ontology. Bioinformatics 20(6), pps. 979-81. (link to paper)