| ggepitracks2 | R Documentation | 
Plot genome tracks for NGS data using ggplot2, resembling GBrowse/JBrowse/IGV style (ver.2 for enhanced performance). Supporting coverage data in bigWig or bedGraph format from RNA-seq, sRNA-seq, BS-seq, ChIP-seq, RIP-seq, GRO-seq, NET-seq, DNase-seq, MNase-seq, ATAC-seq, SHAPE-seq etc. Especially optimized for BS-seq data in single-base resolution. Requires bigWigToBedGraph and bedtools on Linux.
ggepitracks2(
  locus_file,
  track_conf,
  bsseq_conf = NULL,
  gene_model,
  ann_region = NULL,
  ann_color = "goldenrod1",
  out_dir = "out",
  height = NULL,
  width = 80
)
locus_file | 
 BED file containing locus to plot. For each line, TAB-delimited information should contain: <chr>, <start>, <end>, <locus_name>, without header.  | 
track_conf | 
 Configuration file containing track info. For each line, TAB-delimited information should contain: <track_name>, <track_type>, <track_bw/bg>, <y_min>, <y_max>, <color>, <group>, without header. NOTE: If you write "BS-seq" in "<track_type>", provide mC type (one of CG, CHG, CHH, All) to plot in "<track_bw/bg>" and provide detailed info in   | 
bsseq_conf | 
 Configuration file of BS-seq track. If there is no BS-seq track to plot, keep   | 
gene_model | 
 BED file containing all elements of gene and/or TE model, generated by   | 
ann_region | 
 BED file of annotation regions. If not provided, no annotation will be added. For each line, TAB-delimited information should contain: <chr>, <start>, <end>, <annotation_name>, without header. <annotation_name> could be empty but the last TAB should be kept.  | 
ann_color | 
 Color of annotated regions, defalut "goldenrod1" (alpha 30)  | 
out_dir | 
 Path to output directory, will be created if not exist, default "out/". Output plots in PDF format will be saved as <out_dir>/<locus_name>.pdf  | 
height | 
 Plot height, in "mm", defalut 6*ntracks+10  | 
width | 
 Plot width, in "mm", defalut 80  | 
Yujie Liu
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