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base.cfg
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base.cfg
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## COLOURS and transparency for alignments (syntenic, inverted, translocated, and duplicated)
syncol:#CCCCCC
invcol:#FFA500
tracol:#9ACD32
dupcol:#00BBFF
synlwd:0 ## Line width for syntenic annotations
invlwd:0.1 ## Line width for inversions
tralwd:0.1 ## Line width for translocations
duplwd:0.1 ## Line width for duplications
alpha:0.8
## Margins and dimensions:
chrmar:0.1 ## Adjusts the gap between chromosomes and tracks. Higher values leads to more gap
exmar:0.1 ## Extra margin at the top and bottom of plot area
marginchr:0.1 ## Margin between adjacent chromosomes when using --itx
## Legend
legend:T ## To plot legend use T, use F to not plot legend
genlegcol:-1 ## Number of columns for genome legend, set -1 for automatic setup
bbox:0,1.01,0.5,0.3 ## [Left edge, bottom edge, width, height]
bbox_v:0,1.1,0.5,0.3 ## For vertical chromosomes (using -v option)
bboxmar:0.5 ## Margin between genome and annotation legends
## Tracks
norm:T ## For each chromosome, independently normalise the y-axis of tracks. Use T for normalising independently, and F to normalise based on max value across all chromosomes
## Axis
maxl:-1 ## Manually set maximum chromosome position. Use `-1` for automatic selection. Does not work with --itx
genname:T ## Write genome names adjacent to the chromosome (T) or not (F)