Tools to calculate how similar the expression patterns of probes on the Affymetrix array follow that of a "driver" gene of interest.
Analysis options:
- Coexpression analysis in the specified experiment
- Coexpression analysis over available array experiments
- Co-correlation scatter plot
- Clique Finder
- Word Counter
- GO Term Counter
- Keyword Search
Need help? See FAQ
1. Coexpression analysis in the specified experiment
2. Coexpression analysis over available array experiments.
Example analysis:
1. Ribosomal protein
At4g12600 (254831_at);
2. Heat shock protein
At2g20560 (263374_at);
3. Chlorophyll A/B binding protein
At3g61470 (251325_s_at);
3. Co-correlation scatter plot (2-D Pearson Correlation Coefficients)
* Highlighted probe IDs: This is useful to compare the expression patterns of, for example:
- all members of a gene family;
- all genes encoding sub-units of a multi-protein complex, e.g. ribosome;
- a set of genes from your own microarray experiments;
- the genes encoding enzymes of a biochemical pathway;
Please note: There is a small possibility that the scatter plot will re-use the probe ids from the previous query. If you notice this, please refresh the scatter plot page to resend the new probe ids and this should result in an updated scatter plot.
4. Clique Finder over available array experiments.
Example analysis:
1. Ribosomal protein
At4g12600 (254831_at);
2. Heat shock protein
At2g20560 (263374_at);
3. Chlorophyll A/B binding protein
At3g61470 (251325_s_at);
5. Word count of Coexpression analysis over available array experiments.
Example analysis:
1. Ribosomal protein
At4g12600 (254831_at);
2. Heat shock protein
At2g20560 (263374_at);
3. Chlorophyll A/B binding protein
At3g61470 (251325_s_at);
6. Gene Ontology term count of Coexpression analysis over available array experiments.
Example analysis:
1. Ribosomal protein
At4g12600 (254831_at);
2. Heat shock protein
At2g20560 (263374_at);
3. Chlorophyll A/B binding protein
At3g61470 (251325_s_at);
7. Keyword search of annotations for genes of interest
8. Frequently asked questions
How is the correlation coefficient calculated?
What equation do you use to calculate the correlation coefficient?
How do I interpret the correlation list for my gene?
What is the significance of the r-value, p-value and E-values?
How do I decide where the cut-off is between significantly correlated genes versus irrelevant genes?
What do the results from the Word and GO counting tools tell me?
Why is the r-value of the best-correlated gene (other than the driver) so low, e.g. 0.5?
My favourite gene is expressed at a very low level; will it be correlated with other (random?) unexpressed genes?
What a mixture of genes! Can there be any connection between them?!
My gene is correlated with many genes annotated as "hypothetical protein" or "expressed protein" - what does this mean?
What tissues and experimental treatments are represented in the ACT database? Does the dataset include data from mutants as well as wild-type plants?
What other tools are available on the Web to do similar jobs?
How is your correlation tool different from clustering?
Why do you use Affymetrix probe IDs as the input for the correlation analysis rather than the AGI codes?
What's the difference between the Affymetrix ATH1 and AtGenome arrays?
There is much more NASC array data available than you've used in your database; why have you not used it all?
Why have you only used NASC/GARNet array data and not other data sets, such as the Stanford microarray data?
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