Mercurial > repos > estrain > seqsero2_v1_0_1
changeset 4:92d60761a210
Deleted selected files
author | estrain |
---|---|
date | Fri, 06 Sep 2019 04:37:23 -0400 |
parents | 45fff2877ed2 |
children | b4f4b9d54c08 |
files | seqsero.xml.txt |
diffstat | 1 files changed, 0 insertions(+), 175 deletions(-) [+] |
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--- a/seqsero.xml.txt Thu Sep 05 10:02:01 2019 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,175 +0,0 @@ -<tool id="seqsero2_v1_0_1" name="SeqSero 2" version="1.0.1"> - <description>Salmonella serotype prediction</description> - <requirements> - <requirement type="package" version="3.6">python</requirement> - <requirement type="package" version="1.73">biopython</requirement> - <requirement type="package" version="2.7.1">blast</requirement> - <requirement type="package" version="1.9">samtools</requirement> - <requirement type="package" version="2.9.1">sra-tools</requirement> - <requirement type="package" version="0.7.17">bwa</requirement> - <requirement type="package" version="3.13.1">spades</requirement> - <requirement type="package" version="2.27.1">bedtools</requirement> - <requirement type="package">salmid</requirement> - </requirements> - <command detect_errors="exit_code"><![CDATA[ - echo "SeqSero 2 v. 1.0.1" ; - #if $reads.reads_select == 'history' - #set $name = $reads.forward.name.split('.')[0].replace(' ','_') - #set $forward = $reads.forward - #set $reverse = $reads.reverse - #else - #set $name = $reads.coll.name.replace(' ', '_') - #set $forward = $reads.coll.forward - #set $reverse = $reads.coll.reverse - #end if - echo $name ; - echo "-=-=-=-=-" ; - #if $forward.is_of_type('fastq.gz', 'fastqsanger.gz') - gunzip -c $forward > forward.fastq; - #set $forward = './forward.fastq' - #end if - #if $reverse.is_of_type('fastq.gz', 'fastqsanger.gz') - gunzip -c $reverse > reverse.fastq; - #set $reverse = './reverse.fastq' - #end if - ln -s $forward ${name}_1.fastq; - ln -s $reverse ${name}_2.fastq; - mkdir ./output; - touch output/SeqSero_log.txt ; - python $__tool_directory__/SeqSero2_package.py - -p \${GALAXY_SLOTS:-4} - -t 2 - -m $mode - -d ./output - #if $mode == 'a': - -b $maptype - #end if - -i ${name}_1.fastq ${name}_2.fastq && - echo "-=-=-=-=-" && - cat output/SeqSero_log.txt && - echo "-=-=-=-=-" && - ls -lah ./output - ]]></command> - <inputs> - - <conditional name="reads"> - <param name="reads_select" type="select" label="Paired-end collection, or two datasets from your history"> - <option value="collection">Paired collection from your history</option> - <option value="history">Two FASTQ datasets from your history</option> - </param> - <when value="collection"> - <param label="Paired reads" name="coll" type="data_collection" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz" collection_type="paired" /> - </when> - <when value="history"> - <param label="Forward reads" type="data" name="forward" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz" /> - <param label="Reverse reads" type="data" name="reverse" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz" /> - </when> - </conditional> - - <!-- <param name="fastq1" type="data" format="fastq" label="FASTQ paired end read 1" /> - <param name="fastq2" type="data" format="fastq" label="FASTQ paired end read 2" /> --> - <!-- <param name="numofthr" type="select" label="Number of threads"> - <option value="1">1</option> - <option value="2">2</option> - <option value="3">3</option> - <option value="4">4</option> --> - <!-- </param> --> - - <param label="Analysis mode" type="select" name="mode"> - <option value="a">allele mode</option> - <option value="k">k-mer mode</option> - </param> - - <param name="maptype" type="select" label="Algorithms for BWA mapping"> - <option value="mem">mem</option> - <option value="sam">sam</option> - </param> - - - - </inputs> - <outputs> - <data format="tabular" label="SeqSero Results" name="results" from_work_dir="output/Seqsero_result.tsv"/> - </outputs> - <tests> - <!-- <test> - <param name="reads_select" value="history" /> - <param name="forward" value="forward.fastq.gz" ftype="fastqsanger.gz" /> - <param name="reverse" value="reverse.fastq.gz" ftype="fastqsanger.gz" /> - <output name="results" file="Seqsero_result.tsv" /> - </test> - <test> - <param name="reads_select" value="collection" /> - <param name="coll"> - <collection type="paired"> - <element name="forward" value="forward.fastq.gz" ftype="fastqsanger.gz" /> - <element name="reverse" value="reverse.fastq.gz" ftype="fastqsanger.gz" /> - </collection> - </param> - <output name="results" file="Seqsero_result.tsv" /> - </test> --> - <test> - <param name="mode" value="k" /> - <param name="reads_select" value="history" /> - <param name="forward" value="forward_25k.fastq.gz" ftype="fastqsanger" /> - <param name="reverse" value="reverse_25k.fastq.gz" ftype="fastqsanger" /> - <output name="results" file="Seqsero_result_25k.tsv" /> - </test> - <test> - <param name="mode" value="k" /> - <param name="reads_select" value="collection" /> - <param name="coll"> - <collection type="paired"> - <element name="forward" value="forward_25k.fastq.gz" ftype="fastqsanger.gz" /> - <element name="reverse" value="reverse_25k.fastq.gz" ftype="fastqsanger.gz" /> - </collection> - </param> - <output name="results" file="Seqsero_result_25k_coll.tsv" /> - </test> - <test> - <param name="mode" value="a" /> - <param name="reads_select" value="history" /> - <param name="forward" value="forward_250k.fastq.gz" ftype="fastqsanger" /> - <param name="reverse" value="reverse_250k.fastq.gz" ftype="fastqsanger" /> - <assert_stdout> - <has_text text="predicted antigenic profile does not exist" /> - </assert_stdout> - </test> - <!-- <test> - <param name="mode" value="a" /> - <param name="reads_select" value="collection" /> - <param name="coll"> - <collection type="paired"> - <element name="forward" value="forward_25k.fastq.gz" ftype="fastqsanger.gz" /> - <element name="reverse" value="reverse_25k.fastq.gz" ftype="fastqsanger.gz" /> - </collection> - </param> - <output name="results" file="Seqsero_result_allele.tsv" /> - </test> --> - </tests> - <help><![CDATA[ - -**Usage: SeqSero2.py** - -**Algorithms for BWA mapping** - -'mem' for mem, 'sam' for samse/sampe; default=mem; optional; for now SeqSero2 is only optimized for "mem" mode - - ]]></help> - <citations> - <citation type="bibtex"> - @misc{zhang_yin_jones_zhang_deathrage_dinsmore_fitzgeral_fields_deng_2015, - title={Salmonella serotype determination utilizing high-throughput genome sequencing data.}, - journal={J Clin Microbiol}, publisher={ASM}, - author={Zhang S, Yin Y, Jones MB, Zhang Z, Deatherage Kaiser BL, Dinsmore BA, Fitzgerald C, Fields PI, Deng X.}, - year={2015}, month={Max}, - url={http://http://jcm.asm.org/content/early/2015/03/05/JCM.00323-15}}, - }</citation> - <citation type="bibtex"> - @misc{cfsan_biostatistics_group_2017, - title={CFSAN Biostatistics Group fork of SeqSero2}, - url={https://github.com/CFSAN-Biostatistics/SeqSero2.git}}, - </citation> - </citations> - -</tool> \ No newline at end of file