View source: R/coverage_heatmaps.R
heatMapRegion | R Documentation |
Simplified input space for easier abstraction of coverage heatmaps
Pick your transcript region and plot directly
Input CAGE file if you use TSS and want improved 5' annotation.
heatMapRegion(
df,
region = "TIS",
outdir = "default",
scores = c("transcriptNormalized", "sum"),
type = "ofst",
cage = NULL,
plot.ext = ".pdf",
acceptedLengths = 21:75,
upstream = c(50, 30),
downstream = c(29, 69),
shifting = c("5prime", "3prime"),
longestPerGene = TRUE,
colors = "default",
scale_x = 5.5,
scale_y = 15.5,
gradient.max = "default",
BPPARAM = BiocParallel::SerialParam()
)
df |
an ORFik |
region |
a character, default "TIS". The centering point for the heatmap
(what is position 0, beween -50 and 50 etc), can be any combination of the
set: c("TSS", "TIS", "TTS", "TES"), which are:
- Transcription start site (5' end of mrna) |
outdir |
a character path, default: "default", saves to:
|
scores |
character vector, default |
type |
character, default: "ofst". Type of library: either "default", usually bam format (the one you gave to experiment), "pshifted" pshifted reads, "ofst", "bed", "bedo" optimized bed, or "wig" |
cage |
a character path to library file or a |
plot.ext |
a character, default ".pdf", alternative ".png" |
acceptedLengths |
an integer vector (NULL), the read lengths accepted. Default NULL, means all lengths accepted. |
upstream |
1 or 2 integers, default c(50, 30), how long upstream from 0 should window extend (first index is 5' end extension, second is 3' end extension). If only 1 shifting, only 1 value should be given, if two are given will use first. |
downstream |
1 or 2 integers, default c(29, 69), how long upstream from 0 should window extend (first index is 5' end extension, second is 3' end extension). If only 1 shifting, only 1 value should be given, if two are given will use first. |
shifting |
a character, default c("5prime", "3prime"), can also be NULL (no shifting of reads). If NULL, will use first index of 'upstream' and 'downstream' argument. |
longestPerGene |
logical, default TRUE. Use only longest transcript isoform per gene. This will speed up your computation. |
colors |
character vector, default: "default", this gives you: c("white", "yellow2", "yellow3", "lightblue", "blue", "navy"), do "high" for more high contrasts, or specify your own colors. |
scale_x |
numeric, how should the width of the single plots be scaled, bigger the number, the bigger the plot |
scale_y |
numeric, how should the height of the plots be scaled, bigger the number, the bigger the plot |
gradient.max |
numeric or character, default: "default", which is:
|
BPPARAM |
a core param, default: single thread: |
invisible(NULL), plots are saved
Other heatmaps:
coverageHeatMap()
,
heatMapL()
,
heatMap_single()
# Toy example, will not give logical output, but shows how it works
df <- ORFik.template.experiment()[9:10,] # Subset to 2 Ribo-seq libs
#heatMapRegion(df, "TIS", outdir = "default")
#
# Do also TSS, add cage for specific TSS
# heatMapRegion(df, c("TSS", "TIS"), cage = "path/to/cage.bed")
# Do on pshifted reads instead of original files
remove.experiments(df) # Remove loaded experiment first
# heatMapRegion(df, "TIS", type = "pshifted")
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