Mercurial > repos > galaxytrakr > aws_sra

annotate aws_sra.xml @ 18:5680c31cd031 draft

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planemo upload for repository https://github.com/CFSAN-Biostatistics/galaxytrakr-tools commit 593c33d4de9fd7663766c8463d56e4defd608b04
author galaxytrakr
date Mon, 23 Mar 2026 20:51:03 +0000
parents 9fb80e0392ce
children a4186132e1c4
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5680c31cd031 planemo upload for repository https://github.com/CFSAN-Biostatistics/galaxytrakr-tools commit 593c33d4de9fd7663766c8463d56e4defd608b04
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1 <tool id="aws_sra" name="NCBI SRA AWS Fetch" version="0.3.0+gt_0.18" profile="23.0">
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2 <description>Fetches SRA runs from AWS and converts them to FASTQ</description>
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3 <requirements>
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4 <requirement type="package" version="2.34.8">awscli</requirement>
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5 <requirement type="package" version="3.2.1">sra-tools</requirement>
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6 <requirement type="package" version="2.8">pigz</requirement>
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7 </requirements>
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8 <version_command>fasterq-dump --version</version_command>
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10 <command detect_errors="aggressive"><![CDATA[
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11 ## Single Run Mode
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12 #if $run_type.mode == 'single'
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13 #set $acc = str($run_type.accession).strip()
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14 echo "Processing single accession: $acc" &&
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15 mkdir -p sra_cache fastq_out &&
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16 aws s3 cp --no-sign-request 's3://sra-pub-run-odp/sra/${acc}/${acc}' ./sra_cache/ &&
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17 fasterq-dump --outdir ./fastq_out --temp . --threads \${GALAXY_SLOTS:-4} --split-files ./sra_cache/${acc} &&
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18 pigz -p \${GALAXY_SLOTS:-4} ./fastq_out/*.fastq &&
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19 #if str($layout) == 'paired'
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20 mv ./fastq_out/${acc}_1.fastq.gz '$output_r1_single' &&
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21 mv ./fastq_out/${acc}_2.fastq.gz '$output_r2_single'
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22 #else
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23 mv ./fastq_out/*.fastq.gz '$output_r1_single'
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24 #end if
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25
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26 ## Batch Run Mode
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27 #else
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28 #for $acc in $run_type.accession_list.lines:
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29 #set $acc = $acc.strip()
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30 #if $acc:
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31 echo "Processing batch accession: $acc" &&
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32 mkdir -p sra_cache_${acc} fastq_out_${acc} &&
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33 aws s3 cp --no-sign-request 's3://sra-pub-run-odp/sra/${acc}/${acc}' ./sra_cache_${acc}/ &&
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34 fasterq-dump --outdir ./fastq_out_${acc} --temp . --threads \${GALAXY_SLOTS:-4} --split-files ./sra_cache_${acc}/${acc} &&
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35 pigz -p \${GALAXY_SLOTS:-4} ./fastq_out_${acc}/*.fastq &&
9fb80e0392ce planemo upload for repository https://github.com/CFSAN-Biostatistics/galaxytrakr-tools commit 9707fa5e3ca6db5b58f271d133484d078cf65390
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36 #if str($layout) == 'paired'
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37 # Move files to the special path for collection discovery
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38 mv ./fastq_out_${acc}/${acc}_1.fastq.gz '$output_r1_batch.files_path/${acc}_1.fastq.gz' &&
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39 mv ./fastq_out_${acc}/${acc}_2.fastq.gz '$output_r2_batch.files_path/${acc}_2.fastq.gz'
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40 #else
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41 mv ./fastq_out_${acc}/*.fastq.gz '$output_r1_batch.files_path/${acc}.fastq.gz'
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42 #end if &&
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43 rm -rf sra_cache_${acc} fastq_out_${acc}
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44 #end if
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45 #end for
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46 #end if
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47 ]]></command>
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49 <inputs>
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50 <conditional name="run_type">
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51 <param name="mode" type="select" label="Execution Mode">
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52 <option value="single" selected="true">Single Accession</option>
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53 <option value="batch">Batch of Accessions</option>
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54 </param>
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55 <when value="single">
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56 <param name="accession" type="text" label="SRA Accession"/>
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57 </when>
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58 <when value="batch">
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59 <param name="accession_list" type="data" format="txt" label="List of SRA Accessions"/>
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60 </when>
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61 </conditional>
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62 <param name="layout" type="select" label="Read layout">
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63 <option value="paired" selected="true">Paired-end (R1 + R2)</option>
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64 <option value="single">Single-end</option>
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65 </param>
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66 </inputs>
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68 <outputs>
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69 <!-- Outputs for Single Run Mode -->
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70 <data name="output_r1_single" format="fastqsanger.gz" label="${run_type.accession}_1.fastq.gz">
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71 <filter>run_type['mode'] == 'single'</filter>
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72 </data>
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73 <data name="output_r2_single" format="fastqsanger.gz" label="${run_type.accession}_2.fastq.gz">
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74 <filter>run_type['mode'] == 'single' and layout == 'paired'</filter>
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75 </data>
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76
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77 <!-- Outputs for Batch Mode -->
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78 <collection name="output_r1_batch" type="list" label="FASTQ Reads (R1)">
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79 <discover_datasets pattern="(?P&lt;designation&gt;.+)_1\.fastq\.gz" format="fastqsanger.gz" />
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80 <filter>run_type['mode'] == 'batch'</filter>
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81 </collection>
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82 <collection name="output_r2_batch" type="list" label="FASTQ Reads (R2)">
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83 <discover_datasets pattern="(?P&lt;designation&gt;.+)_2\.fastq\.gz" format="fastqsanger.gz" />
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84 <filter>run_type['mode'] == 'batch' and layout == 'paired'</filter>
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85 </collection>
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86 </outputs>
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87
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88 <help><![CDATA[
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89 **NCBI SRA AWS Fetch**
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90
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91 Fetches SRA runs from the public `sra-pub-run-odp` bucket on Amazon S3 and converts them to gzip-compressed FASTQ using `fasterq-dump`.
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92
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93 This tool can be run on a single SRA accession or a list of accessions provided as a text file (one per line).
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94
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95 Outputs are automatically organized into collections suitable for downstream analysis.
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96 ]]></help>
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97
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98 <citations>
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99 <citation type="bibtex">
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100 @misc{ncbi_sra_aws,
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101 title = {{NCBI} {SRA} on {AWS} Open Data},
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102 author = {{National Center for Biotechnology Information}},
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103 howpublished = {\\url{https://registry.opendata.aws/ncbi-sra/}},
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104 note = {Accessed via AWS S3 without credentials}
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105 }
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106 </citation>
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107 <citation type="bibtex">
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108 @article{sra_toolkit,
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109 title = {The {NCBI} {SRA} and portable data in biology},
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110 author = {Leinonen, Rasko and Sugawara, Hideaki and Shumway, Martin and
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111 {International Nucleotide Sequence Database Collaboration}},
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112 journal = {Nucleic Acids Research},
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113 volume = {39},
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114 number = {suppl\\\_1},
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115 pages = {D19--D21},
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116 year = {2011},
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117 doi = {10.1093/nar/gkq1019}
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118 }
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119 </citation>
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120 </citations>
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121 </tool>