View source: R/genomicAnnotation.R
createIntUCSCTrack | R Documentation |
Create a dataframe of sequencing run ids associated with 1 or more patient identifiers.
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)
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'. |
Nothing.
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