GV Exercise.4
Find differentially expressed genes and perform functional enrichment
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last edit: October 31, 2014
Contents
- 1 Aim
- 2 Find perturbations where metacaspases are differentially expressed
- 3 Use |2| fold change and pval <0.05 to restrict the heatmap to most significant treatments for the leftmost probe (ATMCPB1 / LOL3)
- 4 Create a new Sample Selection out of Ath.all based on the filtered perturbations
- 5 Change now to the Anatomy tab and click on probe headers to resort the lines
- 6 Change now to the Development tab and look at the plant stages for metacaspase expression levels
- 7 Apply Gene Ontology Enrichment to the list of caspases with PLAZA
- 8 Perform GSEA with the Plant GSEA web-portal
- 9 Download the exercise files
Aim
Use the Condition Search Tools to identify Samples, Anatomy, Neoplasm (when applies), Perturbations, or Deverlopment annotations that are significantly linked to a list of probes.
Find perturbations where metacaspases are differentially expressed
- select Ath.all as Sample Selection on the top-left of the window and metacaspases as Gene selection at the bottom-left.
- open the Condition Search Perturbations tool
- change the data display to heatmap-list; if using -tree, choose expand all
We get a nice but very long heatmap with many lines showing little if any differential expression
Note the two popups on the right, it allows filtering for more pronounced effects and get shorter heatmaps
Use |2| fold change and pval <0.05 to restrict the heatmap to most significant treatments for the leftmost probe (ATMCPB1 / LOL3)
- How many treatments are kept?
- Which other metacaspase(s) often show DE (UR and DR) for the same treatments?
Create a new Sample Selection out of Ath.all based on the filtered perturbations
Name your new Sample Selection: ATMCPB1_filtered-pert, it will be used later and was saved as part of ex4.gv4 (see bottom of this page).
Change now to the Anatomy tab and click on probe headers to resort the lines
- Set the Sample selection back to Ath.all
- Which tissues do show the highest (lowest) potential expression for the leftmost probe? Are other probes sharing a similar pattern?
Change now to the Development tab and look at the plant stages for metacaspase expression levels
- Alternate between Scatterpot and Heatmap display to estimate which view fits you best.
- export the results to an excel formatted Development-metacaspases.xls file on your laptop then open this file using installed software (eg. libre-office)
metacaspases during development (scatter or heatmap) | |
---|---|
Apply Gene Ontology Enrichment to the list of caspases with PLAZA
Copy the list of TAIR IDs from the exported file or from below
list of TAIR10 IDs for metacaspases
AT1G02170
AT5G64240
AT1G79310
AT1G79320
AT1G79330
AT5G04200
AT4G25110
AT1G79340
AT1G16420
Register to gain access to PLAZA (dicot fro Ath) then log-in and navigate to Analyze' // 'workbench (http://bioinformatics.psb.ugent.be/plaza/versions/plaza_v3_dicots/workbench/logon[1])
Create a new experiment and paste the metacaspase list in the provided text box, save the result with a meaningful title
In the section dedicated to Viewing, pick .. the GO enrichment
GO enrichment metacaspases | |
---|---|
Perform GSEA with the Plant GSEA web-portal
Copy the list of TAIR IDs from the exported file or from below
list of TAIR10 IDs for metacaspases
AT1G02170
AT5G64240
AT1G79310
AT1G79320
AT1G79330
AT5G04200
AT4G25110
AT1G79340
AT1G16420
Navigate to Plant GSEA (http://structuralbiology.cau.edu.cn/PlantGSEA/[2]) Paste the metacaspase list in the Analysis page and select what applies (run the tool)
Inspect the resulting tables (not reproduced here) and the bottom matrix.
GO enrichment metacaspases (2013: left, 2014: right) | |
---|---|
Download the exercise files
Try it by yourself before expanding on the right!
References:
- ↑ http://bioinformatics.psb.ugent.be/plaza/versions/plaza_v3_dicots/workbench/logon
- ↑ http://structuralbiology.cau.edu.cn/PlantGSEA/
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