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1 <tool id="bedtools_genomecoveragebed_bedgraph" name="Create a BedGraph of genome coverage" version="0.1.0">
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2
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3 <description>
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4 </description>
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5
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6 <requirements>
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7 <requirement type="binary">genomeCoverageBed</requirement>
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8 </requirements>
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9
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10 <command>genomeCoverageBed
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11 #if $input.ext == "bam"
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12 -ibam '$input'
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13 #else
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14 -i '$input'
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15 -g ${chromInfo}
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16 #end if
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17
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18 #if str($scale):
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19 -scale $scale
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20 #end if
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21
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22 -bg
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23 $zero_regions
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24 $split
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25 $strand
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26 > '$output'
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27 </command>
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28
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29 <inputs>
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30 <param format="bed,bam" name="input" type="data" label="The BAM or BED file from which coverage should be computed">
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31 <validator type="unspecified_build" />
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32 </param>
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33
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34 <param name="zero_regions" type="boolean" checked="true" truevalue="-bga" falsevalue="" label="Report regions with zero coverage" help="If set, regions without any coverage will also be reported." />
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35
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36 <param name="split" type="boolean" checked="false" truevalue="-split" falsevalue="" label="Treat split/spliced BAM or BED12 entries as distinct BED intervals when computing coverage." help="If set, the coverage will be calculated based the spliced intervals only. For BAM files, this inspects the CIGAR N operation to infer the blocks for computing coverage. For BED12 files, this inspects the BlockCount, BlockStarts, and BlockEnds fields (i.e., columns 10,11,12). If this option is not set, coverage will be calculated based on the interval's START/END coordinates, and would include introns in the case of RNAseq data." />
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37
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38 <param name="strand" type="select" label="Calculate coverage based on">
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39 <option value="">both strands combined</option>
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40 <option value="-strand +">positive strand only</option>
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41 <option value="-strand -">negative strand only</option>
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42 </param>
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43
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44 <param name="scale" type="text" optional="true" 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)"/>
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45 </inputs>
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46
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47 <outputs>
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48 <data format="bedgraph" name="output" metadata_source="input" label="${input.name} (Genome Coverage BedGraph)" />
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49 </outputs>
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50 <help>
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51
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52
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53 **What it does**
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54
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55 This tool calculates the genome-wide coverage of intervals defined in a BAM or BED file and reports them in BedGraph format.
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56
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57 .. class:: warningmark
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58
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59 The input BED or BAM file must be sorted by chromosome name (but doesn't necessarily have to be sorted by start position).
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60
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61 .. class:: warningmark
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62
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63 This tool requires that `bedtools`__ has been installed on your system.
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64
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65 -----
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66
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67 **Example 1**
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68
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69 Input (BED format)-
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70 Overlapping, un-sorted intervals::
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71
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72 chr1 140 176
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73 chr1 100 130
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74 chr1 120 147
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75
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76
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77 Output (BedGraph format)-
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78 Sorted, non-overlapping intervals, with coverage value on the 4th column::
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79
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80 chr1 100 120 1
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81 chr1 120 130 2
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82 chr1 130 140 1
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83 chr1 140 147 2
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84 chr1 147 176 1
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85
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86 -----
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87
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88 **Example 2 - with ZERO-Regions selected (assuming hg19)**
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89
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90 Input (BED format)-
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91 Overlapping, un-sorted intervals::
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92
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93 chr1 140 176
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94 chr1 100 130
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95 chr1 120 147
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96
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97
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98 Output (BedGraph format)-
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99 Sorted, non-overlapping intervals, with coverage value on the 4th column::
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100
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101 chr1 0 100 0
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102 chr1 100 120 1
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103 chr1 120 130 2
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104 chr1 130 140 1
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105 chr1 140 147 2
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106 chr1 147 176 1
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107 chr1 176 249250621 0
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108
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109
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110 This tool is part of the `bedtools package`__ from the `Quinlan laboratory`__. If you use this tool, please cite `Quinlan AR, and Hall I.M. BEDTools: A flexible framework for comparing genomic features. Bioinformatics, 2010, 26, 6.`__
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111
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112 .. __: http://code.google.com/p/bedtools/
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113 .. __: http://code.google.com/p/bedtools/
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114 .. __: http://cphg.virginia.edu/quinlan/
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115 .. __: http://bioinformatics.oxfordjournals.org/content/26/6/841.short
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116 </help>
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117 </tool>
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