View source: R/processCUTTAG.R
peakCallingSEACR | R Documentation |
CUT&TAG peak calling with SEACR
peakCallingSEACR( bam_file, path_peaks, gen_sizes, cores = 5, seacr_type = "stingent", seacr_top = 0.01, bedtools_bamtobed = "bedtools bamtobed", bedtools_genomecov = "bedtools genomecov", seacr = "SEACR_1.3.sh" )
path_peaks |
Path for the peak files. |
gen_sizes |
Chromosome sizes to use for bedgraph conversion. |
cores |
Number of threads to use for the analysis. |
seacr_type |
Type of peaks to call with SEACR, either "stringent" (default) or "relaxed." |
seacr_top |
A numeric threshold n between 0 and 1 returns the top n fraction of peaks based on total signal within peaks. Default: 0.01. |
bedtools_bamtobed |
Path or alias of the bedtools bamtobed utility. |
bedtools_genomecov |
Path or alias of the bedtools genomecov utility. |
seacr |
Path or alias of the SEACR utilty. |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.