Mercurial > repos > iuc > sra_tools

annotate fastq_dump.xml @ 13:c38286ea7047 draft

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 686710a7d313b828f1daed20c4055479727f2d91
author iuc
date Wed, 17 Oct 2018 11:44:12 -0400
parents 6c60903f70ac
children f5ea3ce9b9b0
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6c60903f70ac planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 6252dc2340b2fb6c7fdab2bdadfa4779c6f1aefd
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1 <tool id="fastq_dump" name="Download and Extract Reads in FASTA/Q" version="@VERSION@.3">
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2 <description>format from NCBI SRA</description>
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3 <macros>
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4 <import>sra_macros.xml</import>
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5 </macros>
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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6 <expand macro="requirements"/>
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7 <version_command>fastq-dump --version</version_command>
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8 <command detect_errors="exit_code"><![CDATA[
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9
13
c38286ea7047 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 686710a7d313b828f1daed20c4055479727f2d91
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10 @SET_ACCESSIONS@
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11
0
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12 ## Need to set the home directory to the current working directory,
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13 ## else the tool tries to write to home/.ncbi and fails when used
f256cb398262 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 4e83a7f6d542cd3129eb14a142f74c127f91d026
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14 ## with a cluster manager.
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15 export HOME=\$PWD &&
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16 vdb-config --restore-defaults &&
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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17 #if $input.input_select == "file":
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18 fastq-dump --log-level fatal --accession '${input.file.name}'
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19 #else:
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20 vdb-config -s "/repository/user/main/public/root=\$PWD" &&
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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21 ## Do not use prefetch if region is specified, to avoid downloading
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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22 ## the complete sra file.
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23 #if ( str( $adv.region ) == "" ) and ( str( $adv.minID ) == "" ) and ( str( $adv.maxID ) == "" ):
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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24 ASCP_PATH=`command -v ascp` &&
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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25 ASCP_KEY=`dirname \$ASCP_PATH`/asperaweb_id_dsa.openssh || true &&
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26 prefetch -X 200G --ascp-path "\$ASCP_PATH|\$ASCP_KEY" "\$acc" &&
0
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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27 ## Duplicate vdb-config, in case settings changed between prefetch and
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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28 ## dump command.
b723c120161a planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d555f296be01d0c0fa5ac28d28a48cf4ada98297
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29 vdb-config -s "/repository/user/main/public/root=\$PWD" &&
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30 #end if
462ee06c9358 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit 4defaa3ff1c21e2ec39033bfe63ee69471104ede
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31 fastq-dump --accession "\$acc"
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32 --split-files
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33 #end if
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34 --defline-seq '@\$sn[_\$rn]/\$ri'
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35 --defline-qual '+'
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36
0
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37 $adv.split
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38 #if str( $adv.alignments ) == "aligned":
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39 --aligned
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40 #end if
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41 #if str( $adv.alignments ) == "unaligned":
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42 --unaligned
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43 #end if
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44 #if str( $adv.minID ) != "":
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45 --minSpotId "$adv.minID"
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46 #end if
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47 #if str( $adv.maxID ) != "":
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48 --maxSpotId "$adv.maxID"
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49 #end if
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50 #if str( $adv.minlen ) != "":
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51 --minReadLen "$adv.minlen"
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52 #end if
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53 #if str( $adv.readfilter ) != "":
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54 --read-filter "$adv.readfilter"
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55 #end if
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56 #if str( $adv.region ) != "":
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57 --aligned-region "$adv.region"
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58 #end if
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59 #if str( $adv.spotgroups ) != "":
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60 --spot-groups "$adv.spotgroups"
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61 #end if
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62 #if str( $adv.matepairDist ) != "":
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63 --matepair-distance "$adv.matepairDist"
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64 #end if
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65 $adv.clip
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66 $adv.skip_technical
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67
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68 #if str( $outputformat ) == "fastqsanger.gz":
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69 --gzip
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70 #elif str( $outputformat ) == "fastqsanger.bz2":
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71 --bzip2
0
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72 #end if
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73 #if $input.input_select=="file":
1
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74 --stdout
0
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75 "$input.file" > "$output_file"
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76
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77 #elif $input.input_select=="accession_number":
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78 --stdout
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79 "\$acc" > "$output_accession" )
0
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80 #end if
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81
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82 #if $input.input_select=="file_list":
7
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83 ) ; done
1
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84
7
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85 ;
1
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86
7
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87 for i in `ls *.fast* | cut -f 1 -d '_' | uniq` ; do
c7620aa7e1f0 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sra-tools commit d1347141d384ed404f674d7ce408b6769e763ea1
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88 count=`ls \$i* | wc -l` ;
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89 data=(\$(ls -d \$i*));
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90
7
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91 if [ "\$count" -eq 2 ]; then
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92 mv "\${data[0]}" "\${data[0]}"_forward.$outputformat; mv "\${data[1]}" "\${data[1]}"_reverse.$outputformat ;
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93 elif [ "\$count" -eq 1 ]; then
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94 mv "\${data[0]}" "\${data[0]}"__single.$outputformat ;
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95 fi;
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96 done
1
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97
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98
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99 #end if
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100
2
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101
0
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102 ]]>
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103 </command>
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104 <inputs>
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105 <expand macro="input_conditional"/>
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106 <param name="outputformat" type="select" display="radio" label="Select output format" help="Compression will greatly reduce the amount of space occupied by downloaded data. Downstream applications such as a short-read mappers will accept compressed data as input. Consider this example: an uncoimpressed 400 Mb fastq datasets compresses to 100 Mb or 80 Mb by gzip or bzip2, respectively. " argument="--gzip --bzip2">
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107 <option value="fastqsanger.gz">gzip compressed fastq</option>
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108 <option value="fastqsanger">Uncompressed fastq</option>
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109 <option value="fastqsanger.bz2">bzip2 compressed fastq</option>
0
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110 </param>
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111 <section name="adv" title="Advanced Options" expanded="False">
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112 <param name="minID" type="integer" label="Minimum spot ID" optional="true" help="Minimum spot id to be dumped." argument="--minSpotId"/>
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113 <param name="maxID" type="integer" label="Maximum spot ID" optional="true" help="Maximum spot id to be dumped." argument="--maxSpotId"/>
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114 <param name="minlen" type="integer" label="Minimum read length" optional="true" help="Filter by sequence length. Will dump only reads longer or equal to this value." argument="--minReadLen"/>
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115 <param name="split" type="boolean" checked="true" truevalue="--split-spot" falsevalue="" label="Split spot by read pairs" help="Split spots into individual reads." argument="--split-spot"/>
0
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116 <expand macro="alignments"/>
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117 <expand macro="region"/>
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118 <expand macro="matepairDist"/>
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119 <param name="readfilter" type="select" value="" label="filter by value" argument="--read-filter">
0
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120 <option value="">None</option>
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121 <option value="pass">pass</option>
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122 <option value="reject">reject</option>
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123 <option value="criteria">criteria</option>
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124 <option value="redacted">redacted</option>
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125 </param>
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126 <param name="spotgroups" type="text" label="Filter by spot-groups" optional="true" argument="--spot-groups"/>
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127 <param name="clip" type="boolean" truevalue="--clip" falsevalue="" argument="--clip" label="Apply left and right clips" />
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128 <param name="skip_technical" type="boolean" truevalue="--skip-technical" falsevalue="" checked="False" label="Dump only biological reads" argument="--skip-technical"/>
0
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129 </section>
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130 </inputs>
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131 <outputs>
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132 <collection name="list_paired" type="list:paired" label="Pair-end data (fastq-dump)">
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133 <filter>input['input_select'] == "file_list"</filter>
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134
1
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135 <!-- Use named regex group to grab pattern
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136 <identifier_0>_<identifier_1>.fq. Here identifier_0 is the list
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137 identifier in the nested collection and identifier_1 is either
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138 forward or reverse (for instance samp1_forward.fq).
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139 -->
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140
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141 <discover_datasets pattern="(?P&lt;identifier_0&gt;[^_]+)_\d+.fastq_(?P&lt;identifier_1&gt;[^_]+)\.fastqsanger" ext="fastqsanger" />
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142 <discover_datasets pattern="(?P&lt;identifier_0&gt;[^_]+)_\d+.fastq.gz_(?P&lt;identifier_1&gt;[^_]+)\.fastqsanger.gz" ext="fastqsanger.gz" />
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143 <discover_datasets pattern="(?P&lt;identifier_0&gt;[^_]+)_\d+.fastq.bz2_(?P&lt;identifier_1&gt;[^_]+)\.fastqsanger.bz2" ext="fastqsanger.bz2" />
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144 </collection>
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145 <collection name="output_collection" type='list' label="Single-end data (fastq-dump)">
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146 <filter>input['input_select'] == "file_list"</filter>
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147 <discover_datasets pattern="(?P&lt;designation&gt;.+)_\d+.fastq__single\.fastqsanger" directory="." ext='fastqsanger'/>
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148 <discover_datasets pattern="(?P&lt;designation&gt;.+)_\d+.fastq.gz__single\.fastqsanger.gz" directory="." ext='fastqsanger.gz'/>
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149 <discover_datasets pattern="(?P&lt;designation&gt;.+)_\d+.fastq.bz2__single\.fastqsanger.bz2" directory="." ext='fastqsanger.bz2'/>
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150 </collection>
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151 <data format="fastqsanger" name="output_accession" label="${input.accession} (fastq-dump)">
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152 <filter>input['input_select'] == "accession_number"</filter>
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153 <change_format>
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154 <when input="outputformat" value="fastqsanger.gz" format="fastqsanger.gz"/>
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155 <when input="outputformat" value="fastqsanger.bz2" format="fastqsanger.bz2"/>
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156 </change_format>
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157 </data>
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158 <data format="fastqsanger" name="output_file" label="${input.file.name} (fastq-dump)">
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159 <filter>input['input_select'] == "file"</filter>
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160 <change_format>
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161 <when input="outputformat" value="fastqsanger.gz" format="fastqsanger.gz"/>
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162 <when input="outputformat" value="fastqsanger.bz2" format="fastqsanger.bz2"/>
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163 </change_format>
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164 </data>
0
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165 </outputs>
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166 <tests>
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167 <test>
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168 <param name="input_select" value="accession_number"/>
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169 <param name="outputformat" value="fastqsanger"/>
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170 <param name="accession" value="SRR044777"/>
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171 <param name="skip_technical" value="True"/>
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172 <output name="output_accession">
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173 <assert_contents>
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174 <not_has_text text="rRNA_primer"/>
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175 <has_text text="F47USSH02GNP1D" />
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176 </assert_contents>
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177 </output>
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178 </test>
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179 <test>
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180 <param name="input_select" value="accession_number"/>
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181 <param name="outputformat" value="fastqsanger.gz"/>
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182 <param name="accession" value="SRR925743"/>
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183 <param name="maxID" value="5"/>
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184 <output name="output_accession" file="fastq_dump_result.fastq.gz" decompress="True"/>
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185 </test>
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186 <test>
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187 <param name="input_select" value="accession_number"/>
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188 <param name="outputformat" value="fastqsanger"/>
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189 <param name="accession" value="SRR925743"/>
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190 <param name="maxID" value="5"/>
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191 <output name="output_accession" file="fastq_dump_result.fastq" ftype="fastqsanger"/>
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192 </test>
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193 <test>
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194 <param name="input_select" value="file_list"/>
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195 <param name="outputformat" value="fastqsanger"/>
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196 <param name="file_list" value="list_pe"/>
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197 <param name="maxID" value="5"/>
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198 <output_collection name="list_paired" type="list:paired">
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199 <element name="DRR015708">
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200 <element name="forward" file="DRR015708_forward.fastqsanger">
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201 </element>
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202 <element name="reverse" file="DRR015708_reverse.fastqsanger">
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203 </element>
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204 </element>
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205 </output_collection>
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206 </test>
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207 <test>
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208 <param name="input_select" value="file_list"/>
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209 <param name="outputformat" value="fastqsanger"/>
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210 <param name="file_list" value="list_pe2"/>
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211 <param name="maxID" value="5"/>
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212 <output_collection name="list_paired" type="list:paired">
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213 <element name="ERR027433">
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214 <element name="forward" file="ERR027433_forward.fastqsanger">
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215 </element>
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216 <element name="reverse" file="ERR027433_reverse.fastqsanger">
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217 </element>
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218 </element>
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219 </output_collection>
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220 </test>
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221 <test>
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222 <param name="input_select" value="file_list"/>
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223 <param name="outputformat" value="fastqsanger"/>
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224 <param name="file_list" value="list_se"/>
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225 <param name="maxID" value="5"/>
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226 <output_collection name="output_collection" type="list">
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227 <element name="SRR1993644" file="SRR1993644.fastqsanger"/>
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228 </output_collection>
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229 </test>
0
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230 </tests>
7
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231 <help><![CDATA[
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232 **What it does?**
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233
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234 This tool extracts data (in fastq_ format) from the Short Read Archive (SRA) at the National Center for Biotechnology Information (NCBI). It is based on the fastq-dump_ utility of the SRA Toolkit.
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235
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236 **How to use it?**
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237
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238 There are three ways in which you can download data:
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239
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240 1. Data for single accession
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241 2. Multiple datasets using a list of accessions
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242 3. Extract data from already uploaded SRA dataset
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243
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244 Below we discuss each in detail.
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245
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246 ------
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247
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248 **Uploading data for a single accession**
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249
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250 When you type a single accession number (e.g., `SRR1582967`) into **Accession** box and click **Execute** the tool will fetch data for you. It is important to keep the following in mind:
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251
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252 - if data is paired-ended (or mate-paired) the tool will generate a single *interleaved* dataset, in which forward and reverse mates are alternating (see an example dataset below)
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253 - if data is single ended, a standard single fastq dataset will be produced
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254
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255 -----
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256
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257 **Uploading multiple datasets using a list of accessions**
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258
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259 A more realistic scenario is when you want to upload a number of datasets at once. To do this you need a list of accession, where there is only one accession per line (see below for information on how to generate such a file). Once you have this file:
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260
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261 1. Upload it into your history using Galaxy's upload tool
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262 2. Once the list of accessions is uploaded choose *List of SRA accessions, one per line* from **select input type** dropdown
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263 3. Choose uploaded file within the **sra accession list** field
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264 4. Click **Execute**
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265
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266 .. class:: warningmark
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267
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268 Fastq datasets produced by this option will be saved in Galaxy's history as a collection_ - a single history element containing multiple datasets. In fact, two collections will be produced: one containing paired-end data and another containing single-end data. Single-end or pair-end collections may be empty if the accessions provided in the list contain only SINGLE or PAIRED data, respectively.
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269
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270 -----
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271
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272 **Extract data from already uploaded SRA dataset**
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273
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274 If a SRA dataset is present in the history, it can be converted into fastq dataset by setting **select input type** drop-down to *SRA archive in current history*. Just like in the case of extracting data for single accession number the following applies:
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275
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276 - if data is paired-ended (or mate-pair) the tool will generate a single *interleaved* dataset, in which forward and reverse mates are alternating (see example below).
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277 - if data is single ended, a standard fastq dataset will be produced
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278
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279 @ACCESSION_LIST_HOWTO@
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280
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281 -----
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282
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283 **Paired-end (and mate-pair) data in fastq format**
2
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284
7
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285 Paired end datasets can be represented as two individual datasets:
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286
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287 First dataset::
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288
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289 @1/1
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290 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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291 +
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292 EGGEGGGDFGEEEAEECGDEGGFEEGEFGBEEDDECFEFDD@CDD<ED
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293 @2/1
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294 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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295 +
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296 HHHHHHEGFHEEFEEHEEHHGGEGGGGEFGFGGGGHHHHFBEEEEEFG
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297
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298 Second dataset::
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299
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300 @1/2
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301 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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302 +
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303 GHHHDFDFGFGEGFBGEGGEGEGGGHGFGHFHFHHHHHHHEF?EFEFF
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304 @2/2
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305 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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306 +
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307 HHHHHHHHHHHHHGHHHHHHGHHHHHHHHHHHFHHHFHHHHHHHHHHH
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308
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309 Or a single *interleaved* dataset::
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310
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311 @1/1
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312 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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313 +
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314 EGGEGGGDFGEEEAEECGDEGGFEEGEFGBEEDDECFEFDD@CDD<ED
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315 @1/2
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316 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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317 +
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318 GHHHDFDFGFGEGFBGEGGEGEGGGHGFGHFHFHHHHHHHEF?EFEFF
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319 @2/1
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320 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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321 +
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322 HHHHHHEGFHEEFEEHEEHHGGEGGGGEFGFGGGGHHHHFBEEEEEFG
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323 @2/2
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324 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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325 +
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326 HHHHHHHHHHHHHGHHHHHHGHHHHHHHHHHHFHHHFHHHHHHHHHHH
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327
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328 ----
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329
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330
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331 .. _fastq: https://en.wikipedia.org/wiki/FASTQ_format
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332 .. _fastq-dump: https://ncbi.github.io/sra-tools/fastq-dump.html
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333 .. _collection: https://galaxyproject.org/tutorials/collections/
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334 .. _link: http://www.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=studies
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335
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336 @SRATOOLS_ATTRRIBUTION@
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337
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338 ]]>
0
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339 </help>
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340 <expand macro="citation"/>
1
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341 </tool>