createIntUCSCTrack: Annotate genomic ranges

View source: R/genomicAnnotation.R

createIntUCSCTrackR Documentation

Annotate genomic ranges

Description

Create a dataframe of sequencing run ids associated with 1 or more patient identifiers.

Usage

createIntUCSCTrack(d, abundCuts = c(5, 10, 50),
  posColors = c("#8C9DFF", "#6768E3", "#4234C7", "#1D00AB"),
  negColors = c("#FF8C8C", "#E35D5D", "#C72E2E", "#AB0000"),
  title = "intSites", outputFile = "track.ucsc", visibility = 1,
  position = "chr7:127471196-127495720", padSite = 0, siteLabel = NA)

Arguments

d

Data fram containing genomic ranges to be added to UCSC track.

abundCuts

Cut points for estimated abundance (estAbund) values.

posColors

Color codes for binned abundances (positive integrations).

negColors

Color codes for binned abundances (positive integrations).

title

Track title.

outputFile

Track output file.

visibility

Track default visibility (0 - hide, 1 - dense, 2 - full, 3 - pack, and 4 - squish).

position

Deafult track position.

padSite

Number of NTs to pad sites with for increased visibility.

siteLabel

Text to appear next to sites, ie. 'Patient X, chr12+1052325'.

Value

Nothing.


everettJK/gt23 documentation built on May 16, 2024, 12:04 p.m.