Question: How to separate chip-seq peaks which are enriched for known TFs motifs from given list of peaks
1
gravatar for Naresh D J
4.4 years ago by
Naresh D J80
Turku/BTK
Naresh D J80 wrote:

Dear All,

I have a list of enhancer marks in terms of peaks file from chip-seq data (three column, chr, start, end) and run motif analysis using HOMER software (http://homer.salk.edu/homer/). It did gave few known and de novo enriched motifs. I want to identify the peaks which are enriched with these TFs motifs from the initial list of peaks.

Does anybody has ideas/suggestions to achieve this? Is it possible at all?

Thank you.

ADD COMMENTlink modified 4.3 years ago by ivivek_ngs5.0k • written 4.4 years ago by Naresh D J80

How about FIMO?

ADD REPLYlink written 4.4 years ago by jotan1.2k

I second that. You can run FIMO in your list of peaks to know which ones have the motif.

ADD REPLYlink written 4.4 years ago by Fidel1.9k
0
gravatar for Naresh D J
4.3 years ago by
Naresh D J80
Turku/BTK
Naresh D J80 wrote:

There is a script in HOMER itself for finding the instances of the enriched motifs in the input of chip-seq peaks. "annotatepeaks.pl"

ADD COMMENTlink written 4.3 years ago by Naresh D J80

You can use HOMER motif finder for the same, for finding both de novo and known motifs as well.

ADD REPLYlink written 4.3 years ago by ivivek_ngs5.0k
0
gravatar for ivivek_ngs
4.3 years ago by
ivivek_ngs5.0k
Seattle,WA, USA
ivivek_ngs5.0k wrote:

You can also use C-SCAN for chip-seq data by taking into account the refseq id for the peaks if they are already annotated. This will give you a single output of which TFs are likely to be common regulators of the genes from the peaks.

ADD COMMENTlink modified 4.3 years ago • written 4.3 years ago by ivivek_ngs5.0k
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