# HG changeset patch
# User jjohnson
# Date 1655122172 0
# Node ID 1d459aaa5765a23f05f31a8ca589a0d7107a1570
# Parent 73fd7703a7433365b7c776505bab4ce863ee1b70
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/arriba commit 25fe476002a414e72f33868ba356a3ca4f86865d"
diff -r 73fd7703a743 -r 1d459aaa5765 arriba.xml
--- a/arriba.xml Tue Apr 26 20:35:35 2022 +0000
+++ b/arriba.xml Mon Jun 13 12:09:32 2022 +0000
@@ -13,6 +13,10 @@
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+ By default all filters are enabled.
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Arriba estimates the number of fusions with a given number of supporting
reads which one would expect to see by random chance. If the expected number
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diff -r 73fd7703a743 -r 1d459aaa5765 macros.xml
--- a/macros.xml Tue Apr 26 20:35:35 2022 +0000
+++ b/macros.xml Mon Jun 13 12:09:32 2022 +0000
@@ -1,5 +1,5 @@
- 2.2.1
+ 2.3.00
@@ -49,6 +49,7 @@
+
By default the transcript isoform with the highest coverage is drawn.
Alternatively, the transcript isoform that is provided in the columns
@@ -81,14 +82,6 @@
-
- This option only applies to intergenic breakpoints.
- If it is set to a value greater than 0, then the script draws the genes
- which are no more than the given distance away from an intergenic breakpoint.
- Note that this option is incompatible with squishIntrons.
- Default: 0
-
-
Exons usually make up only a small fraction of a gene.
They may be hard to see in the plot. i
@@ -100,7 +93,24 @@
-
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+ This option only applies to intergenic breakpoints.
+ If it is set to a value greater than 0, then the script draws the genes
+ which are no more than the given distance away from an intergenic breakpoint.
+ The keywords closestGene and closestProteinCodingGene instruct the script
+ to dynamically determine the distance to the next (protein-coding) gene for each breakpoint.
+ Alternatively, instead of specifying a single distance
+ that is applied upstream and downstream of both breakpoints alike,
+ more fine-grained control over the region to be shown is possible by specifying four comma-separated values.
+ The first two values determine the region to the left and to the right of breakpoint 1;
+ the third and fourth values determine the region to the left and to the right of breakpoint 2.
+ Note that this option is incompatible with squishIntrons.
+ Default: 0
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+ ^(closestGene|closestProteinCodingGene|\d+|\d+,\d+,\d+,\d+)$
+
Occasionally, domains are annotated redundantly.
For example, tyrosine kinase domains are frequently annotated as
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help="Default: 8.267"/>
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+ Default: Helvetica
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+ By default, transcripts are scaled automatically to fill the entire page.
+ This parameter enforces a fixed scale to be applied to all fusions,
+ which is useful when a collection of fusions should be visualized and the sizes of all transcripts should be comparable.
+ A common use case is the visualization of a gene that is found to be fused to multiple partners.
+ By forcing all fusion plots to use the same scale, the fusions can be summarized as a collage
+ in a single plot one above the other with matching scales.
+ Note: The scale must be bigger than the sum of the biggest pair of transcripts to be drawn,
+ or else dynamic scaling is applied, because display errors would occur otherwise.
+ The default value is 0, which means that no fixed scale should be used
+ and that the scale should be adapted dynamically for each fusion. Default: 0
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+ When the parameter --alignments is used, coverage plots are drawn above the transcripts of the fused genes.
+ The plots can be cropped at a fixed level by passing a non-zero value to this parameter.
+ When only a single value is given, both coverage plots (for gene1 and gene2) are cropped at the same level.
+ When two comma-separated values are given, the cutoffs can be specified independently for the two plots.
+ A value of 0 indicates that no cropping should be applied (i.e., the cutoff is set to the peak coverage)
+ and that the coverage plots of both genes should be on the same scale. This is the default behavior.
+ A value of 0,0 also indicates that no cropping should be applied,
+ but the coverage plots of the two genes have different scales:
+ each one is scaled individually to the peak coverage of the respective gene.
+ Default: 0
+
+ ^\d+(,\d+)?$
+
@@ -172,18 +243,24 @@
#if $visualization.options.minConfidenceForCircosPlot
--minConfidenceForCircosPlot=$visualization.options.minConfidenceForCircosPlot
#end if
- #if $visualization.options.showIntergenicVicinity
- --showIntergenicVicinity=$visualization.options.showIntergenicVicinity
- #end if
#if $visualization.options.squishIntrons
--squishIntrons=$visualization.options.squishIntrons
+ #if $visualization.options.squishIntrons == 'FALSE' and $visualization.options.showIntergenicVicinity
+ --showIntergenicVicinity=$visualization.options.showIntergenicVicinity
+ #end if
#end if
#if $visualization.options.mergeDomainsOverlappingBy
--mergeDomainsOverlappingBy=$visualization.options.mergeDomainsOverlappingBy
#end if
+ #if $visualization.options.sampleName
+ --sampleName=$visualization.options.sampleName
+ #end if
#if $visualization.options.printExonLabels
--printExonLabels=$visualization.options.printExonLabels
#end if
+ #if $visualization.options.coverageRange
+ --coverageRange="$visualization.options.coverageRange"
+ #end if
#if $visualization.options.render3dEffect
--render3dEffect=$visualization.options.render3dEffect
#end if
@@ -202,6 +279,10 @@
#if $visualization.options.pdfHeight
--pdfHeight=$visualization.options.pdfHeight
#end if
+ # fontFamily
+ #if $visualization.options.fontFamily
+ --fontFamily=$visualization.options.fontFamily
+ #end if
#if $visualization.options.fontSize
--fontSize=$visualization.options.fontSize
#end if