Visualizes genomic breakpoints resulting from copy-number aberrations (amplifications and deletions) and chromosomal rearrangements (translocations and inversions).
Creates a bar plot that shows number of breakpoints in each chromosome (grouped by breakpoint type) and for each chromosome a figure with a scatter plot and a histogram of the locations of the breakpoints.
WARNING: Loads the whole data into memory twice, so beware of using big data.
Also note that this is an early version, and assumes specific columns for the inputs.
Version | 0.1.1 |
---|---|
Bundle | sequencing |
Categories | VariationAnalysis |
Authors | Viljami Aittomaki (viljami.aittomaki@helsinki.fi) |
Issue tracker | View/Report issues |
Requires | R ; ggplot2 (R-package) ; gridExtra (R-package) |
Source files | component.xml BreakpointVisualizer.r |
Usage | Example with default values |
Name | Type | Mandatory | Description |
---|---|---|---|
cna | CSV | Mandatory | Copy-number aberration data. |
rearrangements | CSV | Mandatory | Chromosomal rearrangement data, i.e. translocations and inversions. |
Name | Type | Description |
---|---|---|
report | Latex | The visualizations as a Latex fragment. |
Name | Type | Default | Description |
---|---|---|---|
binwidth | int | 100000 | Width of bins for histogram in bp. Small bins can be slow to compute. |