Question: Problems with MACS peak calling--FDRs of 100%
gravatar for jm.keith
23 months ago by
jm.keith60 wrote:

Hello, I am having some issues with MACS peak calling. I have 5 files in my ChIP-Seq dataset (input, p300, H3K4me, H3K27Ac and a TF file)--for the histone modification and TF files, I am able to call peaks nicely with in-range FDR%. With the p300 files, however, I am unable to call peaks without FDR % all being very high. My question is why is this happening and how might I correct for this?

My files were aligned using Bowtie for Illumina, then duplicate reads were removed with a run through the Rmdup tool and these are the parameters that I am using:

MACS (on the Rmdup output files)

Effective genome size 1870000000.0

Tag size 40

Band width 300

Pvalue cutoff for peak detection 1e-05

Select the regions with MFOLD high-confidence enrichment ratio against background to build model 40

Parse xls files into into distinct interval files Yes

Use fixed background lambda as local lambda for every peak region Yes

Build the shifting model

Perform the new peak detection method (futurefdr) Yes

Many thanks for any assistance.


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