Visualize TF Sites on Sequences

Overview of visualize TF sites on sequences tool
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

Enter Enhancer DNA sequence(s)
One or more named DNA sequences to be annotated.
Sequence name*
Name of the Enhancer.
Sequence*
DNA Sequence of the Enhancer. Only use upper case A/T/C/G.
Annotate TF with relative affinity
Annotate TF with PWM binding scores
Required PWM score to predict a site. Does not apply to PWMs referenecd in the "tf information tsv" file. Default is 0.7.
Other Parameters
Option to output images as SVG in addition to PNG. SVG are preferable for manuscript preparation.
Enter the resolution for the plot in DPI (dots per inch).
Optional: Given a start position and an end position, zoom into a portion of the sequence. The numbers in the range are inclusive. For example, the first 200 nucleotides of the sequence would be specified as: 1-200. Leave blank if not applicable.