ChIP-seq differential binding analysis tools
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Consensus peaksets in DiffBind - conceptual questinos
written by Aspire1- The DiffBind vignette (section 8.2 - Deriving consensus peaksets) states > When performing an overlap analysis, it is often the case that the > …
-
CUT&Tag data processing: peak caller choice and typical peak size profile
written by nihilior •Greetings everyone, I am currently analysing CUT&Tag data (a recent technique, variant of the ChIP-seq), capturing different histone variants. To do so, I tried all …
-
MACS2 sample grouping
written by Beth •Hi all, I have a question about sample grouping when calling peaks using MACS2: I have data from two studies containing Input and H3K27ac samples …
-
ATAC-Seq: Filter bams for differential analysis or not
written by srhic •Hello, I am doing some analysis to identify differential accessible regions between two conditions using atac-seq. The workflow I have followed uses peak calling with …
-
Are MACS2's summit or DiffBind's summit options are recommended for histone marks like H3K4me3, H3K…
written by ResearcherHi All I have used MACS2 for the peak calling with no summit at the default settings and then used Diffbind to call differential peak …
-
Downstream of Csaw differential binding region
written by Jingyue •Dear all, I have a question of downstream analysis after I got the differential binding (DB) region from Csaw tool, which used a window-based method. …
-
How to find out whether Chip-seq peaks falls within promoter or enhancer region of gene?
written by crazyscientist •Hello, I have analyzed the ChIP-seq data. I have used MACS2 for peak calling. In result of that, I have data with the peaks and …
-
how to find differential region between my replicates.
written by maryamforoozani16 •Hello , I did chip experiment with three replicates for two conditions ( normal condition(C) and phosphate deficiency condition (P)) on Rice genome. I tried …
-
peaks overlap: ATAC & CHIP seq
written by sophialovechan •Hi guys. I have two peak files. One is from ATAC seq and the other is from H3K27ac chip seq. I am trying to merge …
-
Union Peaks For Peaks Called On Different Strains
written by Sander Timmer<p>For a bunch of strains we have Chip-Seq on which we have been calling peaks using SWEMBL. We now want to generate an union peak …
I do not see why you would want to do that. It only makes things more complicated. If you want to be more stringent better lower the FDR cutoff from like 10% to 5 or 1% or test against a certain fold change, e.g. 1.5, using
glmTreatincsaw(the actual function comes fromedgeR). Combining different tools is tricky as one would need to ensure that normalization, filtering etc. is more or less identical to have a meaningful analysis.