In this panel, you can see some basic information about the adjusted ChIP-seq experiments: name; antibody; cell line and element number (The number of peak regions obtained in a ChIP-seq experiment, which overlap with a particular consensus motif binding site set). The background colours indicate the histogram colours of the experiments on the plot.
The histograms shows the summit distance distributions of the selected ChIP-seq data (a maximum of 3) related to a motif center. The PairShiftView allows users to examine the distribution of individual summi- consensus motif distances for three experiments. To smooth the graph, a 5 bp rolling bin is used in the histogram. Each curve represents one ChIP-seq experiment. The X axis represents the distance (measured in base pairs) from the middle of the given motif, which is marked as the “0” point. The numbering of the axis is consistent with the position weight matrix below the diagram. The Y axis shows the frequency of summit occurrences at the relative position (at a given base pair) relative to the motif center. In the case of well-defined protein topology with high overlap frequency and close DNA localization, the curve has a bell-like pattern (normal distribution-like).
These setting can filter the displayed data. You can set the minimum and maximum element number. After updating the page with “Refresh Page” button, the experiments with out of range values will be vanished from plot.
Select a motif from the dropdown box and click on the ”Refresh Page” button. After updating the page, you can invetigate the occupying proteins on the instances of the adjusted transcription factor motif.
SummitDB SummitDB

Shift values are shown using the 'FOXA1' motif's center as point zero.

Experiment name Antibody Cell line Element number
hs_BreastCancer_T47D_cancer_FOXA1_SRX100454 FOXA1 T47D 53298
hs_HepatocellularCarcinoma_HepG2_cancer_FOXA1_SRX100506 FOXA1 HEPG2 60468
hs_VertebralCancerOfProstate_VCaP_cancer_FOXA1_SRX497612 FOXA1 VCAP 68559

Position weight matrix of selected motif.


The following buttons will navigate you to different views of currently plotted data.

Minimum overlap number between motifs and peaks of experiment: 100


Set a motif:


Select the experiments in the rows of boxes below. Set from left to right: cell type > name of antibody > experiment. Then click on “Resend data” button to refresh the page.

cell type

antibody

experiment name




In the boxes below set the minimum and maximum distances from the centre of the motif. This is the value of x axis.


distance from motif center maximum


distance from motif center minimum


When the parameters have been set, this button will refresh the page.

If you want to start the selection and filtering the experiment list via antibody name, then use the following panels. Select the experiments in the rows of boxes below. Set from left to right: name of antibody > cell type > experiment. Then click on “Refresh Page” button to refresh the page.

antibody

cell type

experiment name





PairShiftView

In this mode, the frequencies of the different distance values between the motif and peak summit pairs for a given consensus binding site set are displayed in a histogram. To smooth the graph a 5 bp rolling bin was used. No more than three different experiments can be compared. The height of the curves shows the most frequent distance. In the PairShiftView mode, the data range and the consensus motif binding site can be set. An experiment can be also selected and displayed in the ExperimentView.