| Literature DB >> 15980551 |
Bernhard Mlecnik1, Marcel Scheideler, Hubert Hackl, Jürgen Hartler, Fatima Sanchez-Cabo, Zlatko Trajanoski.
Abstract
While generation of high-throughput expression data is becoming routine, the fast, easy, and systematic presentation and analysis of these data in a biological context is still an obstacle. To address this need, we have developed PathwayExplorer, which maps expression profiles of genes or proteins simultaneously onto major, currently available regulatory, metabolic and cellular pathways from KEGG, BioCarta and GenMAPP. PathwayExplorer is a platform-independent web server application with an optional standalone Java application using a SOAP (simple object access protocol) interface. Mapped pathways are ranked for the easy selection of the pathway of interest, displaying all available genes of this pathway with their expression profiles in a selectable and intuitive color code. Pathway maps produced can be downloaded as PNG, JPG or as high-resolution vector graphics SVG. The web service is freely available at https://pathwayexplorer.genome.tugraz.at; the standalone client can be downloaded at http://genome.tugraz.at.Entities:
Mesh:
Year: 2005 PMID: 15980551 PMCID: PMC1160152 DOI: 10.1093/nar/gki391
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971
The number of unique gene identifiers (e.g. Homo sapiens) available for mapping expression profiles in PathwayExplorer
| Pathway resource | No. of pathways | Unique RefSeq accession no. | Unique GenBank accession no. | Unique UniGene accession no. | Unique GO accession no. |
|---|---|---|---|---|---|
| KEGG | 120 | 4099 | 26589 | 2827 | 2561 |
| BioCarta | 311 | 2209 | 15889 | 1438 | 1671 |
| GenMAPP | 82 | 6374 | 38171 | 4527 | 2857 |
| Sum | 513 | 8947 | 55111 | 6276 | 3623 |
The table shows the sum of non-redundant accession numbers available.
Figure 1PathwayExplorer example: a screenshot of a pathway mapped with expression data. (i) The toolbar frame (the row including the organism field) offers various setup and visualization options. (ii) Hierarchical tree frame (on the left) enables browsing through all available pathway sections. (iii) The main frame (in the center) displays the citrate cycle pathway extracted from KEGG, which mapped with a yeast sporulation data set with seven different time points (0, 0.5, 2, 5, 7, 8 and 11.5 h). The color-coded boxes represent mapped genes. If more than just one gene ID (e.g. RefSeq) matches to a box, each box is split up into several horizontal elements. According to the number of experiments/time points (in this case seven time points), the boxes are split again into vertical columns which display the expression level of each time point. To visualize a mapped expression profile in a different way, one has to choose the corresponding horizontal row of a box (see Figure 2).
Figure 3(a) Shows the overall statistic of the filtered unique identifiers of the expression data set mapped on all pathways. (b) The ranking list of all mapped pathways is also displayed and can be sorted by different criteria, allowing easy navigation through all pathways. By selecting the pathway of interest, the data set will be automatically mapped on the pathway and the expression values will be displayed in a selectable and intuitive color code (see Figure 1). The last two columns display the P-value and the FDR (19) corrected Q-value.
2 × 2 contingency table for the Fisher's exact test
| Genes that are differentially expressed (passed the filter) | Gene that are not differentially expressed (filtered out) | ||
|---|---|---|---|
| Mapped genes | A | B | A+B |
| Unmapped genes | C | D | C+D |
| A+C | B+D | Total number of genes |
The null hypothesis of the right-tailed Fisher's exact test states that the proportion of A/C is smaller or equal to the proportion of B/D. If the right-tailed P-value is <5%, we reject the null hypothesis, which means that the proportion of differentially expressed genes is significantly greater than those that are not differentially expressed.
Figure 2By selecting one row (if there are more than one) of a mapped gene box (Figure 1), the corresponding gene and expression profile information will be displayed. To obtain additional information links to GenBank, Entrez and OMIM are provided. Only one mapped expression profile from the uploaded data set can be displayed at once.