Difference between revisions of "Analyze promoters (TRANSFAC(R)) (workflow)"
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[[File:Analyze-promoters-TRANSFAC-R-workflow-overview.png|400px]] | [[File:Analyze-promoters-TRANSFAC-R-workflow-overview.png|400px]] | ||
== Description == | == Description == | ||
| − | This workflow is designed to search for putative transcription factor binding | + | This workflow is designed to search for putative transcription factor binding sites (TFBS) in the promoters of an input gene set. |
As input, any gene or protein table can be submitted. The input table contains genes under study, and it is called “Yes” set. | As input, any gene or protein table can be submitted. The input table contains genes under study, and it is called “Yes” set. | ||
| − | At the first step, the | + | At the first step, promoters are analyzed for potential cis-regulatory sites. Promoters in this workflow are defined as sequences from -1000 to +100 relative to the transcription start sites, as they are annotated in Ensembl. |
| − | At the | + | Site search is done with the help of the TRANSFAC® library of the positional weight matrices (PWMs), namely with the default profile (matrix collection) vertebrate_non_redundant_minSUM. At the same step, frequencies of putative TFBSs are compared between Yes set and No set to identify sites overrepresented in Yes set versus No set. Default No set in the workflow is a set of housekeeping genes for the corresponding species (as they are published in PMID: 19534766) |
| − | + | The result of this step is a list of transcription factor binding sites, which are overrepresented in Yes set versus No set. | |
| − | + | Next, the list of PWMs is converted into a table of corresponding transcription factors and are annotated with additional information (gene description and gene symbols). | |
| − | + | The output is a new folder with several tables, including a summary of the predicted TFBSs, genomic tracks of the Yes and No promoters and their sites. As well as the final table with transcription factors, that are potentially regulating the genes in the Yes set. | |
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| − | + | ||
| − | The output is a new folder with several tables, including a summary of the predicted TFBSs, genomic tracks of the Yes and No | + | |
This workflow is available together with a valid TRANSFAC® license. | This workflow is available together with a valid TRANSFAC® license. | ||
== Parameters == | == Parameters == | ||
| − | ;Input gene set | + | ;Input gene set (Yes set) |
| + | ;Profile | ||
;Species | ;Species | ||
| + | ;No set | ||
| + | ;5<nowiki>'</nowiki> flank | ||
| + | :Position relative to TSS, bp | ||
| + | ;3<nowiki>'</nowiki> flank | ||
| + | :Position relative to TSS, bp | ||
;Results folder | ;Results folder | ||
[[Category:Workflows]] | [[Category:Workflows]] | ||
| + | [[Category:GeneXplain workflows]] | ||
[[Category:Autogenerated pages]] | [[Category:Autogenerated pages]] | ||
Latest revision as of 16:34, 12 March 2019
- Workflow title
- Analyze promoters (TRANSFAC(R))
- Provider
- geneXplain GmbH
[edit] Workflow overview
[edit] Description
This workflow is designed to search for putative transcription factor binding sites (TFBS) in the promoters of an input gene set.
As input, any gene or protein table can be submitted. The input table contains genes under study, and it is called “Yes” set.
At the first step, promoters are analyzed for potential cis-regulatory sites. Promoters in this workflow are defined as sequences from -1000 to +100 relative to the transcription start sites, as they are annotated in Ensembl.
Site search is done with the help of the TRANSFAC® library of the positional weight matrices (PWMs), namely with the default profile (matrix collection) vertebrate_non_redundant_minSUM. At the same step, frequencies of putative TFBSs are compared between Yes set and No set to identify sites overrepresented in Yes set versus No set. Default No set in the workflow is a set of housekeeping genes for the corresponding species (as they are published in PMID: 19534766)
The result of this step is a list of transcription factor binding sites, which are overrepresented in Yes set versus No set.
Next, the list of PWMs is converted into a table of corresponding transcription factors and are annotated with additional information (gene description and gene symbols).
The output is a new folder with several tables, including a summary of the predicted TFBSs, genomic tracks of the Yes and No promoters and their sites. As well as the final table with transcription factors, that are potentially regulating the genes in the Yes set.
This workflow is available together with a valid TRANSFAC® license.
[edit] Parameters
- Input gene set (Yes set)
- Profile
- Species
- No set
- 5' flank
- Position relative to TSS, bp
- 3' flank
- Position relative to TSS, bp
- Results folder
