Mercurial > repos > yhoogstrate > segmentation_fold

annotate utils_extract-boxed-sequences.xml @ 16:7e5b96d45f8d draft

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planemo upload for repository https://github.com/ErasmusMC-Bioinformatics/segmentation_fold_galaxy_wrapper commit c6608bd5256e5c54cb2e01be6c184da0d2b08a7c-dirty
author yhoogstrate
date Thu, 19 May 2016 05:41:48 -0400
parents 487f438da099
children 3fbde4864e00
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1 <tool id="smf_utils_extract-boxed-sequences" name="extract-boxed-sequences" version="@VERSION@-0">
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2 <description>Extracts boxed sequences from bed_input_file which has to be created with 'find-box', part of this utility</description>
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4 <macros>
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5 <import>macros.xml</import>
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6 </macros>
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8 <requirements>
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9 <requirement type="package" version="2.7.10">python</requirement>
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10 <requirement type="package" version="1.9">numpy</requirement>
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11 <requirement type="package" version="0.8.2.1">pysam</requirement>
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12 <requirement type="package" version="2.0.0">segmentation-fold-utils</requirement>
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13 </requirements>
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14 <expand macro="stdio" />
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16 <version_command>@VERSION_COMMAND_UTILS@</version_command>
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18 <command><![CDATA[
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19 segmentation-fold-utils
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20 extract-boxed-sequences
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22 --max-inner-dist $max_inner_dist
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23 --bp-extension $bp_extension
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24
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25 '${fasta_input_file}'
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26 '${bed_input_file}'
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27 '${fasta_output_file}'
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29 ]]></command>
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31 <inputs>
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32 <param name="fasta_input_file"
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33 type="data"
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34 format="fasta"
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35 label="Genomic reference FASTA file"/>
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36 <param name="bed_input_file"
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37 type="data"
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38 format="bed"
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39 label="BED file containing the sequence boxes"
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40 help="This file should have been created with 'find-boxes'"/>
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42 <param name="max_inner_dist"
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43 type="integer"
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44 min="0"
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45 value="250"
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46 label="Maximal distance between the boxes"
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47 help="(default=250bp)"/>
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48 <param name="bp_extension"
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49 type="integer"
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50 min="0"
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51 value="10"
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52 label="Extend extracted sequences with this number of bases"
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53 help="(default: 10bp)"/>
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54 </inputs>
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55
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56 <outputs>
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57 <data name="fasta_output_file"
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58 format="fasta"
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59 label="${tool.name} on ${fasta_input_file.hid}: ${fasta_input_file.name}"/>
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60 </outputs>
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61
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62 <tests>
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63 <test>
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64 <param name="fasta_input_file" value="ExtractBoxedSequences.test_01.in.fa" ftype="fasta"/>
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65 <param name="bed_input_file" value="ExtractBoxedSequences.test_01.in.bed" ftype="bed"/>
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66 <param name="max_inner_dist" value='100'/>
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67 <param name="bp_extension" value='0'/>
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68
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69 <output name="fasta_output_file" file="ExtractBoxedSequences.test_01.out.fa"/>
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70 </test>
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71 </tests>
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72
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73 <help><![CDATA[
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74 extact-boxed-sequences
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75 ----------------------
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76 *Extracts boxes sequences from `bed_input_file` which has to be created with 'find-box', also part of this utility*
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77
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78 The user can use this utility to extract sequences containing the boxes provided in the bed file by `find-boxes`.
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80 **input**
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81
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82 Important information about the input:
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83
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84 - `FASTA_INPUT_FILE` can be any generic FASTA file that can be read with pysam. This means that if the sequence is split into multiple lines, they must all be at the same length.
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85 - `BED_INPUT_FILE` the bed file should be provided by `find-boxes` as it properly denotes the names (box1-f, box1-r, box2-f and box2-r) which are used for extraction.
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86 - `-d, --max-inner-dist INTEGER` Only sequences for which the distance in bases between the boxes is smaller than this distance, will be extracted. Boxes are excluded from this distance.
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87 - `-e, --bp-extension INTEGER` Each sequence will be exteded with:
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88 * The boxes
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89 * An optional number of bases provided with this argument
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90
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91 **output**
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92
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93 Be aware that there can be overlapping sequences. For example, if you started box1=`TTTT` and box2=`CCCC` with the following sequence, you will extract 2 sequences:
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94
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95 ```>seq
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96 gagagaTTTTgagagaTTTTgagagagagagagagaCCCCgaga
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97 ```
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98
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99 Namely:
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100
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101 ```TTTTgagagaTTTTgagagagagagagagaCCCC
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102 ```
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103
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104 and
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105
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106 ``` TTTTgagagagagagagagaCCCC
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107 ```
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108
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109 This is an utility of the segmentation-fold package
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110 ]]></help>
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111
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112 <expand macro="citations" />
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113 </tool>