Mercurial > repos > peterjc > seq_primer_clip
annotate tools/seq_primer_clip/seq_primer_clip.xml @ 2:ee5acea162a7 draft
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author | peterjc |
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date | Thu, 24 Oct 2013 09:37:25 -0400 |
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children | 9b074c1db68e |
rev | line source |
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2
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1 <tool id="seq_primer_clip" name="Primer clip sequences" version="0.0.10"> |
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2 <description>Trim off 5' or 3' primers</description> |
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3 <requirements> |
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4 <requirement type="package" version="1.62">biopython</requirement> |
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5 <requirement type="python-module">Bio</requirement> |
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6 </requirements> |
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7 <version_command interpreter="python">seq_primer_clip.py --version</version_command> |
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8 <command interpreter="python"> |
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9 seq_primer_clip.py $input_file $input_file.ext $primer_fasta $primer_type $mm $min_len $keep_negatives $output_file |
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10 </command> |
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11 <stdio> |
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12 <!-- Anything other than zero is an error --> |
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13 <exit_code range="1:" /> |
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14 <exit_code range=":-1" /> |
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15 </stdio> |
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16 <inputs> |
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17 <param name="input_file" type="data" format="fasta,fastq,sff" label="Sequence file to clip" description="FASTA, FASTQ, or SFF format."/> |
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18 <param name="primer_fasta" type="data" format="fasta" label="FASTA file containing primer(s)"/> |
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19 <param name="primer_type" type="select" label="Type of primers"> |
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20 <option value="Forward">Forward (5') primers</option> |
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21 <option value="Reverse">Reverse (3') primers (given with respect to the forward strand)</option> |
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22 <option value="Reverse-complement">Reverse (3') primers (given with respect to the reverse strand)</option> |
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23 </param> |
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24 <param name="mm" type="integer" value="0" label="How many mismatches to allow? (0, 1 or 2)"> |
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25 <validator type="in_range" min="0" max="2" /> |
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26 </param> |
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27 <param name="keep_negatives" type="boolean" value="false" label="Keep reads with no matched primer"/> |
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28 <param name="min_len" type="integer" label="Minimum length for (clipped) sequences " value="1"/> |
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29 </inputs> |
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30 <outputs> |
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31 <data name="output_file" format="data" label="$primer_type primer clipped"> |
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32 <!-- TODO - Replace this with format="input:input_fastq" if/when that works --> |
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33 <change_format> |
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34 <when input_dataset="input_file" attribute="extension" value="sff" format="sff" /> |
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35 <when input_dataset="input_file" attribute="extension" value="fasta" format="fasta" /> |
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36 <when input_dataset="input_file" attribute="extension" value="fastq" format="fastq" /> |
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37 <when input_dataset="input_file" attribute="extension" value="fastqsanger" format="fastqsanger" /> |
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38 <when input_dataset="input_file" attribute="extension" value="fastqsolexa" format="fastqsolexa" /> |
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39 <when input_dataset="input_file" attribute="extension" value="fastqillumina" format="fastqillumina" /> |
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40 <when input_dataset="input_file" attribute="extension" value="fastqcssanger" format="fastqcssanger" /> |
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41 </change_format> |
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42 </data> |
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43 </outputs> |
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44 <tests> |
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45 <test> |
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46 <param name="input_file" value="MID4_GLZRM4E04_rnd30.fasta" ftype="fasta" /> |
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47 <param name="primer_fasta" value="dop_primers.fasta" /> |
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48 <param name="primer_type" value="Forward" /> |
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49 <param name="mm" value="2" /> |
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50 <param name="keep_negatives" value="false" /> |
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51 <param name="min_len" value="35" /> |
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52 <output name="output_file" file="MID4_GLZRM4E04_rnd30_fclip.fasta" ftype="fasta" /> |
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53 </test> |
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54 <test> |
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55 <param name="input_file" value="MID4_GLZRM4E04_rnd30.fastqsanger" ftype="fastqsanger" /> |
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56 <param name="primer_fasta" value="dop_primers.fasta" /> |
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57 <param name="primer_type" value="Forward" /> |
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58 <param name="mm" value="2" /> |
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59 <param name="keep_negatives" value="false" /> |
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60 <param name="min_len" value="35" /> |
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61 <output name="output_file" file="MID4_GLZRM4E04_rnd30_fclip.fastqsanger" ftype="fastqsanger" /> |
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62 </test> |
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63 <test> |
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64 <param name="input_file" value="MID4_GLZRM4E04_rnd30.sff" ftype="sff" /> |
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65 <param name="primer_fasta" value="dop_primers.fasta" /> |
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66 <param name="primer_type" value="Forward" /> |
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67 <param name="mm" value="2" /> |
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68 <param name="keep_negatives" value="false" /> |
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69 <param name="min_len" value="35" /> |
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70 <output name="output_file" file="MID4_GLZRM4E04_rnd30_fclip.sff" ftype="sff" /> |
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71 </test> |
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72 <test> |
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73 <param name="input_file" value="MID4_GLZRM4E04_rnd30_fclip.fasta" ftype="fasta" /> |
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74 <param name="primer_fasta" value="dop_primers.fasta" /> |
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75 <param name="primer_type" value="Reverse" /> |
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76 <param name="mm" value="2" /> |
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77 <param name="keep_negatives" value="true" /> |
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78 <param name="min_len" value="35" /> |
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79 <output name="output_file" file="MID4_GLZRM4E04_rnd30_frclip.fasta" ftype="fasta" /> |
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80 </test> |
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81 <test> |
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82 <param name="input_file" value="MID4_GLZRM4E04_rnd30_fclip.fastqsanger" ftype="fastqsanger" /> |
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83 <param name="primer_fasta" value="dop_primers.fasta" /> |
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84 <param name="primer_type" value="Reverse" /> |
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85 <param name="mm" value="2" /> |
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86 <param name="keep_negatives" value="true" /> |
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87 <param name="min_len" value="35" /> |
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88 <output name="output_file" file="MID4_GLZRM4E04_rnd30_frclip.fastqsanger" ftype="fastqsanger" /> |
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89 </test> |
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90 <test> |
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91 <param name="input_file" value="MID4_GLZRM4E04_rnd30_fclip.sff" ftype="sff" /> |
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92 <param name="primer_fasta" value="dop_primers.fasta" /> |
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93 <param name="primer_type" value="Reverse" /> |
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94 <param name="mm" value="2" /> |
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95 <param name="keep_negatives" value="true" /> |
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96 <param name="min_len" value="35" /> |
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97 <output name="output_file" file="MID4_GLZRM4E04_rnd30_frclip.sff" ftype="sff" /> |
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98 </test> |
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99 </tests> |
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100 <requirements> |
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101 <requirement type="python-module">Bio</requirement> |
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102 </requirements> |
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103 <help> |
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104 |
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105 **What it does** |
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106 |
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107 Looks for the given primer sequences (within the existing clipped sequence) and |
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108 further clips the reads to remove the primers and any preceding/trailing sequence. |
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109 |
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110 Reads containing a forward primer are reduced to just the sequence after (and |
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111 excluding) the forward primer. |
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112 |
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113 Reads containing a reverse primer are reduced to just the sequence before (and |
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114 excluding) the reverse primer. |
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115 |
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116 Degenerate primers can be specified using the standard IUPAC ambiguity codes, |
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117 thus a primer with an N would match A, C, T or G (or any of the IUPAC ambiguity |
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118 codes) and so on. |
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119 |
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120 Note that for SFF files only the clip/trim positions are edited - you will still |
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121 be able to extract the original full read (with any adapter sequence and poor |
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122 quality sequence) if you need to. |
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123 |
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124 .. class:: warningmark |
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125 |
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126 **Note**. This tool was initially written for Roche 454 data, and should also |
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127 work fine on Sanger or Ion Torrent as well. However, it is probably too slow |
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128 for use on large Illumina datasets. |
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129 |
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130 |
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131 **Citation** |
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132 |
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133 This tool uses Biopython. If you use this tool in scientific work leading to a |
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134 publication, please cite: |
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135 |
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136 Cock et al 2009. Biopython: freely available Python tools for computational |
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137 molecular biology and bioinformatics. Bioinformatics 25(11) 1422-3. |
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138 http://dx.doi.org/10.1093/bioinformatics/btp163 pmid:19304878. |
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139 |
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140 This tool is available to install into other Galaxy Instances via the Galaxy |
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141 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/seq_primer_clip |
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142 </help> |
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143 </tool> |