sparse peak calling
I have a Chipseq data and I expects peaks should be sparse. Which tool may be best to call sparse peaks? Can I also use same tool for calling sparse peaks of cut and Run experiment.
Thanks
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You can try SEACR : https://epigeneticsandchromatin.biomedcentral.com/articles/10.1186/s13072-019-0287-4
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Do you mind defining what you consider sparse peaks?
The low read depths and background levels and broader peaks.
Hi Kanwarjag, why don't you increase the depth of sequencing ? or merge more IP