ggepitracks | R Documentation |
Plot genome tracks for NGS data using ggplot2, resembling GBrowse/JBrowse style. Supporting coverage data in bigWig 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 bedtools
on Linux.
ggepitracks(
locus_file,
track_conf,
bsseq_conf = NULL,
gene_model,
ann_region = NULL,
ann_color = "goldenrod1",
out_dir = "out"
)
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_file>, <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 "<path_to_track_file>" and provide detailed info in |
bsseq_conf |
configuration file of BS-seq track. If no BS-seq track plotted, 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 |
out_dir |
path to output directory, create it if not exist |
Yujie Liu
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