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.