diff bedtools_genomecov/genomeCoverageBed.xml @ 2:3aa9416cc3b3 draft

Uploaded
author jackcurragh
date Fri, 27 May 2022 11:33:45 +0000
parents b63479816ebe
children
line wrap: on
line diff
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/bedtools_genomecov/genomeCoverageBed.xml	Fri May 27 11:33:45 2022 +0000
@@ -0,0 +1,170 @@
+<tool id="bedtools_genomecoveragebed" name="BedTools Genome Coverage" version="@TOOL_VERSION@" profile="@PROFILE@">
+    <description>Compute Read Coverage Over An Entire Genome</description>
+    <macros>
+        <import>macros.xml</import>
+    </macros>
+    <expand macro="bio_tools" />
+    <expand macro="requirements" />
+    <expand macro="stdio" />
+    <command><![CDATA[
+bedtools genomecov
+@GENOME_FILE_COVERAGE@
+
+$split
+$strand
+
+#if str($report.report_select) == "bg":
+    #if $report.zero_regions:
+        $report.zero_regions
+    #else:
+        -bg
+    #end if
+
+    #if str($report.scale):
+        -scale $report.scale
+    #end if
+#else:
+    #if str($report.max):
+        -max $report.max
+    #end if
+#end if
+$d
+$dz
+$five
+$three
+> '$output'
+    ]]></command>
+    <inputs>
+        <conditional name="input_type">
+            <param name="input_type_select" type="select" label="Input type">
+                <option value="bed">@STD_BEDTOOLS_INPUT_LABEL@</option>
+                <option value="bam" selected='true'>BAM</option>
+            </param>
+            <when value="bed">
+                <param name="input" argument="-i" type="data" format="@STD_BEDTOOLS_INPUTS@" label="@STD_BEDTOOLS_INPUT_LABEL@ file" />
+                <expand macro="input_conditional_genome_file" />
+            </when>
+            <when value="bam">
+                <param name="input" argument="-ibam" type="data" format="bam" label="BAM file" />
+            </when>
+        </conditional>
+        <conditional name="report">
+            <param name="report_select" type="select" label="Output type">
+                <option value="bg" selected="true">BedGraph coverage file</option>
+                <option value="hist">Data suiteable for Histogram</option>
+            </param>
+            <when value="bg">
+                <param name="zero_regions" argument="-bga" type="boolean" truevalue="-bga" falsevalue="" checked="false"
+                    label="Report regions with zero coverage" help="If set, regions without any coverage will also be reported" />
+                <param argument="-scale" type="float" value="1.0"
+                    label="Scale the coverage by a constant factor"
+                    help="Each bedGraph coverage value is multiplied by this factor before being reported. Useful for normalizing coverage by, e.g., reads per million (RPM)." />
+            </when>
+            <when value="hist">
+                <param argument="-max" type="integer" value="0" label="Specify max depth"
+                    help="Combine all positions with a depth >= max into a single bin in the histogram" />
+            </when>
+        </conditional>
+        <expand macro="split" />
+        <param argument="-strand" type="select" label="Calculate coverage based on">
+            <option value="">both strands combined</option>
+            <option value="-strand +">positive strand only</option>
+            <option value="-strand -">negative strand only</option>
+        </param>
+
+        <param argument="-d" type="boolean" truevalue="-d" falsevalue="" checked="false"
+            label="Report the depth at each genome position with 1-based coordinates" />
+        <param argument="-dz" type="boolean" truevalue="-dz" falsevalue="" checked="false"
+            label="Report the depth at each genome position with 0-based coordinatess" />
+        <param name="five" argument="-5" type="boolean" truevalue="-5" falsevalue="" checked="false"
+            label="Calculate coverage of 5’ positions" help="Instead of entire interval" />
+        <param name="three" argument="-3" type="boolean" truevalue="-3" falsevalue="" checked="false"
+            label="Calculate coverage of 3’ positions" help="Instead of entire interval" />
+    </inputs>
+    <outputs>
+        <data name="output" format="bedgraph">
+            <change_format>
+                <when input="report.report_select" value="hist" format="tabular" />
+            </change_format>
+        </data>
+    </outputs>
+    <tests>
+        <test>
+            <param name="input_type_select" value="bed" />
+            <param name="input" value="genomeCoverageBed1.bed" ftype="bed" />
+            <param name="genome_file_opts_selector" value="hist" />
+            <param name="genome" value="genomeCoverageBed1.len" ftype="tabular" />
+            <param name="report_select" value="hist" />
+            <output name="output" file="genomeCoverageBed_result1.bed" ftype="tabular" />
+        </test>
+    </tests>
+    <help><![CDATA[
+**What it does**
+
+This tool calculates the genome-wide coverage of intervals defined in a BAM or BED file and reports them in BedGraph format.
+
+.. image:: $PATH_TO_IMAGES/genomecov-glyph.png
+
+.. class:: warningmark
+
+The input BED or BAM file must be sorted by chromosome name (but doesn't necessarily have to be sorted by start position).
+
+-----
+
+**Example 1**
+
+Input (BED format)-
+Overlapping, un-sorted intervals::
+
+    chr1    140 176
+    chr1    100 130
+    chr1    120 147
+
+
+Output (BedGraph format)-
+Sorted, non-overlapping intervals, with coverage value on the 4th column::
+
+    chr1    100 120 1
+    chr1    120 130 2
+    chr1    130 140 1
+    chr1    140 147 2
+    chr1    147 176 1
+
+-----
+
+**Example 2 - with ZERO-Regions selected (assuming hg19)**
+
+Input (BED format)-
+Overlapping, un-sorted intervals::
+
+    chr1    140 176
+    chr1    100 130
+    chr1    120 147
+
+
+BedGraph output will contain five columns:
+
+    * 1. Chromosome name (or 'genome' for whole-genome coverage)
+    * 2. Coverage depth
+    * 3. The number of bases on chromosome (or genome) with depth equal to column 2.
+    * 4. The size of chromosome (or entire genome) in base pairs
+    * 5. The fraction of bases on chromosome (or entire genome) with depth equal to column 2.
+
+**Example Output**:
+
+    chr2L       0           1379895     23011544    0.0599653
+    chr2L       1           837250      23011544    0.0363839
+    chr2L       2           904442      23011544    0.0393038
+    chr2L       3           913723      23011544    0.0397072
+    chr2L       4           952166      23011544    0.0413778
+    chr2L       5           967763      23011544    0.0420555
+    chr2L       6           986331      23011544    0.0428624
+    chr2L       7           998244      23011544    0.0433801
+    chr2L       8           995791      23011544    0.0432735
+    chr2L       9           996398      23011544    0.0432999
+
+
+@REFERENCES@
+    ]]></help>
+    <expand macro="citations" />
+</tool>