Mercurial > repos > matthias > stacks2_clonefilter
diff stacks_clonefilter.xml @ 3:4758a347d62e draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit 9c41b2599125298b1a4d9ffb2511cdc87ff79a73
author | matthias |
---|---|
date | Tue, 18 Dec 2018 13:06:09 -0500 |
parents | 223e7778451a |
children | c4ed7dacee9b |
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--- a/stacks_clonefilter.xml Fri Nov 30 07:42:16 2018 -0500 +++ b/stacks_clonefilter.xml Tue Dec 18 13:06:09 2018 -0500 @@ -7,7 +7,6 @@ <expand macro="stdio"/> <expand macro="version_cmd"/> <command><![CDATA[ - #if $data_type.dt_select == "single" #if $data_type.fname.is_of_type('fastqsanger') @@ -34,7 +33,7 @@ #end if - mkdir clone_outputs + mkdir outputs && @@ -48,12 +47,11 @@ -i $inputype - -o clone_outputs + -o outputs $capture - + $data_type.barcode_encoding #if $oligo_len_1 --oligo_len_1 $oligo_len_1 - $data_type.barcode_encoding #end if #if $oligo_len_2 --oligo_len_2 $oligo_len_2 @@ -62,7 +60,6 @@ ## only supports fastq.gz output since the ## the program outputs empty files for fasta/fastq -y gzfastq - ]]></command> <inputs> <conditional name="data_type"> @@ -73,7 +70,7 @@ <when value="single"> <param name="fname" type="data" format="fastqsanger,fastqsanger.gz" label="FASTQ" /> <param name="barcode_encoding" type="select" label="Barcode location"> - <expand macro="barcode_encoding_single" /> + <expand macro="barcode_encoding_single" type="Random oligo"/> </param> </when> @@ -81,29 +78,30 @@ <param name="fwd" type="data" format="fastqsanger,fastqsanger.gz" label="Forward FASTQ" /> <param name="rev" type="data" format="fastqsanger,fastqsanger.gz" label="Reverse FASTQ" /> <param name="barcode_encoding" type="select" label="Barcode location"> - <expand macro="barcode_encoding_pair" /> + <expand macro="barcode_encoding_pair" type="Random oligo"/> </param> </when> </conditional> <param name="capture" type="boolean" checked="false" truevalue="-D" falsevalue="" argument="-D" label="Capture discarded reads to a file" /> - <param name="oligo_len_1" optional="true" type="integer" label="length of the single-end oligo sequence in data set"/> + <param name="oligo_len_1" type="integer" value="0" label="length of the single-end oligo sequence in data set"/> <param name="oligo_len_2" optional="true" type="integer" label="length of the paired-end oligo sequence in data set"/> <param argument="--retain_oligo" type="boolean" checked="false" truevalue="--retain_oligo" falsevalue="" label="do not trim off the random oligo sequence (if oligo is inline)" /> </inputs> <outputs> - <data format="fastqsanger.gz" name="clean" from_work_dir="clone_outputs/R1.fq.gz" label="${tool.name} on ${on_string}"> + <data format="fastqsanger.gz" name="clean" from_work_dir="outputs/R1.fq.gz" label="${tool.name} on ${on_string}"> <filter>data_type['dt_select'] == 'single'</filter> </data> - <data format="fastqsanger.gz" name="clean_fwd" from_work_dir="clone_outputs/R1.1.fq.gz" label="${tool.name} on ${on_string} Forward reads"> + <data format="fastqsanger.gz" name="clean_fwd" from_work_dir="outputs/R1.1.fq.gz" label="${tool.name} on ${on_string} Forward reads"> <filter>data_type['dt_select'] == 'pair'</filter> </data> - <data format="fastqsanger.gz" name="clean_rev" from_work_dir="clone_outputs/R2.2.fq.gz" label="${tool.name} on ${on_string} Reverse reads"> + <data format="fastqsanger.gz" name="clean_rev" from_work_dir="outputs/R2.2.fq.gz" label="${tool.name} on ${on_string} Reverse reads"> <filter>data_type['dt_select'] == 'pair'</filter> </data> </outputs> <tests> + <!-- single end, defaults--> <test> <conditional name="data_type"> <param name="dt_select" value="single" /> @@ -112,29 +110,44 @@ <param name="oligo_len_1" value="6" /> <output name="clean" compare="sim_size" file="clonefilter/Removed1_0001.1.1.fq.single.gz"/> </test> + <!-- single end, alt BCencoding, capture--> <test> <conditional name="data_type"> <param name="dt_select" value="single" /> <param name="fname" ftype="fastqsanger.gz" value="clonefilter/R1_0001.1.fq.gz" /> <param name="barcode_encoding" value="--index_null" /> </conditional> + <param name="capture" value="-D" /> + <param name="oligo_len_1" value="6" /> + <assert_command> + <has_text text="-D" /> + </assert_command> <output name="clean" compare="sim_size" file="clonefilter/Removed1_0001.1.1.fq.gz"/> </test> + <!-- paired end, defaults--> <test> <conditional name="data_type"> <param name="dt_select" value="pair" /> <param name="fwd" ftype="fastqsanger" value="clonefilter/R1_0001.1.fq.gz" /> <param name="rev" ftype="fastqsanger" value="clonefilter/R2_0001.2.fq.gz" /> </conditional> + <param name="oligo_len_1" value="6" /> <output name="clean_fwd" compare="sim_size" file="clonefilter/Removed1_0001.1.1.fq.gz"/> <output name="clean_rev" compare="sim_size" file="clonefilter/Removed2_0001.2.2.fq.gz"/> </test> + <!-- paired end, non defaults--> <test> <conditional name="data_type"> <param name="dt_select" value="pair" /> <param name="fwd" ftype="fastqsanger.gz" value="clonefilter/R1_0001.1.fq.gz" /> <param name="rev" ftype="fastqsanger.gz" value="clonefilter/R2_0001.2.fq.gz" /> </conditional> + <param name="oligo_len_1" value="6" /> + <param name="capture" value="-D" /> + <param name="retain_oligo" value="--retain_oligo" /> + <assert_command> + <has_text text="--retain_oligo" /> + </assert_command> <output name="clean_fwd" compare="sim_size" file="clonefilter/Removed1_0001.1.1.fq.gz"/> <output name="clean_rev" compare="sim_size" file="clonefilter/Removed2_0001.2.2.fq.gz"/> </test> @@ -143,7 +156,6 @@ <![CDATA[ .. class:: infomark - The clone_filter program is designed to identify PCR clones. @STACKS_INFOS@