Mercurial > repos > greg > vsnp_sample_names
diff vsnp_sample_names.xml @ 0:f75e2ac7b6cd draft
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author | greg |
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date | Tue, 21 Apr 2020 10:17:20 -0400 |
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children | 895d18fcfebe |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/vsnp_sample_names.xml Tue Apr 21 10:17:20 2020 -0400 @@ -0,0 +1,91 @@ +<tool id="vsnp_sample_names" name="vSNP: sample names" version="1.0.0"> + <description></description> + <command detect_errors="exit_code"><![CDATA[ +#import os +#import re +#set output_dir = 'output' +mkdir -p $output_dir +#if str($input_type_cond.input_type) == "single": + ## We may have a single read or a pair, but in + ## either case we want the same base file name. + #set sample_name = $os.path.basename($input_type_cond.read.element_identifier) + #if $sample_name.find(".") > 0: + #set sample_name = $sample_name.split(".")[0] + #end if + #if $sample_name.find("_") > 0: + #set sample_name = $sample_name.split("_")[0] + #end if + echo $sample_name > $output +#else: + #for $i in $input_type_cond.reads_collection: + #set sample_name = $os.path.basename($i.element_identifier) + #if $sample_name.find(".") > 0: + #set sample_name = $sample_name.split(".")[0] + #end if + #set output_file = $os.path.join($output_dir, $sample_name) + && echo $sample_name > $output_file + #end for +#end if +]]></command> + <inputs> + <conditional name="input_type_cond"> + <param name="input_type" type="select" label="Choose the category of the files to be analyzed"> + <option value="single" selected="true">Single files</option> + <option value="collection">Collections of files</option> + </param> + <when value="single"> + <param name="read" type="data" format="fastqsanger.gz,fastqsanger" label="Sample file"/> + </when> + <when value="collection"> + <param name="reads_collection" type="data_collection" format="fastqsanger,fastqsanger.gz" collection_type="list" label="Collection of sample files"/> + </when> + </conditional> + </inputs> + <outputs> + <data name="output" format="txt"> + <filter>input_type_cond['input_type'] == 'single'</filter> + </data> + <collection name="output__collection" type="list"> + <discover_datasets pattern="__name__" directory="output" format="txt" /> + <filter>input_type_cond['input_type'] == 'collection'</filter> + </collection> + </outputs> + <tests> + <test> + <param name="input_type" value="collection"/> + <param name="reads_collection"> + <collection type="list"> + <element name="BCG_Danish_Human_UK_SRR9596061.fastq" value="BCG_Danish_Human_UK_SRR9596061.fastq" dbkey="89"/> + <element name="Dassie_Dassie_ZA_SRR3745455.fastq" value="Dassie_Dassie_ZA_SRR3745455.fastq" dbkey="89"/> + <element name="Mbov_Cattle_NI_SRR10993937.fastq" value="Mbov_Cattle_NI_SRR10993937.fastq" dbkey="89"/> + </collection> + </param> + <output_collection name="output__collection" type="list"> + <element name="BCG_Danish_Human_UK_SRR9596061" file="BCG_Danish_Human_UK_SRR9596061" ftype="txt"/> + <element name="Dassie_Dassie_ZA_SRR3745455" file="Dassie_Dassie_ZA_SRR3745455" ftype="txt"/> + <element name="Mbov_Cattle_NI_SRR10993937" file="Mbov_Cattle_NI_SRR10993937" ftype="txt"/> + </output_collection> + </test> + </tests> + <help> +**What it does** + +Accepts one or more sample files and extracts a unique portion of the file name as the content of the output file(s). These +text files are then used as workflow parameter values for the Read Group Identifier parameter in the bwa-mem tool. + +**Required Options** + + * **Choose the category of the files to be analyzed** - select "Single files" or "Collections of files", then select the appropriate history items (single or paired fastqsanger reads or collections of fastqsanger reads) based on the selected option. + </help> + <citations> + <citation type="bibtex"> + @misc{None, + journal = {None}, + author = {1. Stuber T}, + title = {Manuscript in preparation}, + year = {None}, + url = {https://github.com/USDA-VS/vSNP},} + </citation> + </citations> +</tool> +