Compare TF Sites across Sequences

Predict and visualize TF binding sites on one or multiple enhancers. Sites can be predicted using two approaches. The first and preferred is to predict sites with a core binding site and determine binding site affinity using a reference affinity dataset. When less studies on the TF have been performed, the alternative approach is to use a PWM to predict locations and binding scores. The output is (1) an image visualizing where the predicted sites are along with their affinity or PWM-binding score, and (2) a table with every binding site, its location, direction, affinity and a unique site identifier.
Links: Tutorial Video Documentation

Parameters

Provide a name for this analysis.
Specify the hypothesis to test. LOF, GOF or both Default is "both".
At least two DNA sequences to be analyzed. We suggest only inputting the alignment +/- 15 bp from where the genetic variation of interest occurs. if this is a SNV, you would simply input the 30bp window of the alignment containing the variant. If this is a deletion, you would add 15 bp upstream of the first - and 15bp downstream of the last -.
DNA Name* DNA Alignment* Functional Group*
Labels for each functional group. Functional group can be either wild-type, control, test, or na. If na, all enhancers associated with that label will be removed from the analysis. Binding sites are searched for within the test group that are not present within the wild-type or control group. At a minimum both of these requirements must be met, (1) at least one control or wild-type must be provided; (2) at least one test must be provided.
Group name* Group Label*
*Input one of the following TF datasets:

All the information for the transcription factors being analyzed, including its name, binding site definition, desired color on the plot, any PBM relative affinity data, and any PFM relative score data. You can generate an affinity dataset with the Normalize TF-DNA Affinity Data tool.
TF Name* Core Site* Affinity Data create an affinity dataset download example
or
* Enter the minimum binding change threshold for analysis.