Mercurial > repos > bgruening > bismark
diff bismark_bowtie2_wrapper.xml @ 17:aa9bf0f29a9f draft
"planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/bismark commit d85012b50faac3234496bb51e2a29c2d8c113bde"
author | bgruening |
---|---|
date | Wed, 28 Aug 2019 07:08:45 -0400 |
parents | a4504327c890 |
children | 359f8b60d316 |
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--- a/bismark_bowtie2_wrapper.xml Wed Aug 21 12:59:48 2019 -0400 +++ b/bismark_bowtie2_wrapper.xml Wed Aug 28 07:08:45 2019 -0400 @@ -1,4 +1,4 @@ -<tool id="bismark_bowtie2" name="Bismark Mapper" version="0.22.1+galaxy3" profile="18.01"> +<tool id="bismark_bowtie2" name="Bismark Mapper" version="0.22.1+galaxy4" profile="18.01"> <description>Bisulfite reads mapper</description> <requirements> <requirement type="package" version="0.22.1">bismark</requirement> @@ -12,11 +12,20 @@ #if $singlePaired.input_singles.ext == "fasta": #set read1 = 'input_1.fa' #elif $singlePaired.input_singles.ext in ["fastq.gz", "fastqsanger.gz"]: - #set read1 = 'input_1.fq.gz' + #if $params.pbat == "--pbat" + #set read1 = 'input_1.fq' + #else + #set read1 = 'input_1.fq.gz' + #end if #else #set read1 = 'input_1.fq' #end if - ln -s '${singlePaired.input_singles}' '${read1}' && + + #if $params.pbat == "--pbat" and $singlePaired.input_singles.ext in ["fastq.gz", "fastqsanger.gz"]: + zcat '${singlePaired.input_singles}' > '${read1}' && + #else + ln -s '${singlePaired.input_singles}' '${read1}' && + #end if #else: #set $mate1 = list() #set $mate2 = list() @@ -25,20 +34,38 @@ #if $mate_pair.input_mate1.ext == "fasta": #set read1 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_1.fa' #elif $mate_pair.input_mate1.ext in ["fastq.gz", "fastqsanger.gz"]: - #set read1 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_1.fq.gz' + #if $params.pbat == "--pbat" + #set read1 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_1.fq' + #else + #set read1 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_1.fq.gz' + #end if #else #set read1 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_1.fq' #end if - ln -s '${mate_pair.input_mate1}' '${read1}' && + + #if $params.pbat == "--pbat" and $mate_pair.input_mate1.ext in ["fastq.gz", "fastqsanger.gz"]: + zcat '${mate_pair.input_mate1}' > '${read1}' && + #else + ln -s '${mate_pair.input_mate1}' '${read1}' && + #end if #if $mate_pair.input_mate2.ext == "fasta": #set read2 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_2.fa' #elif $mate_pair.input_mate2.ext in ["fastq.gz", "fastqsanger.gz"]: - #set read2 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_2.fq.gz' + #if $params.pbat == "--pbat" + #set read2 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_2.fq' + #else + #set read2 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_2.fq.gz' + #end if #else #set read2 = re.sub('[^\w\-_.]', '_', str($mate_pair.input_mate1.element_identifier)) + '_2.fq' #end if - ln -s '${mate_pair.input_mate2}' '${read2}' && + + #if $params.pbat == "--pbat" and $mate_pair.input_mate2.ext in ["fastq.gz", "fastqsanger.gz"]: + zcat '${mate_pair.input_mate2}' > '${read2}' && + #else + ln -s '${mate_pair.input_mate2}' '${read2}' && + #end if $mate1.append( str($read1) ) $mate2.append( str($read2) ) @@ -138,6 +165,8 @@ $params.non_directional + $params.pbat + #if $params.bismark_stdout: --stdout '$output_stdout' #end if @@ -289,6 +318,11 @@ <param argument="--non-directional" name="non_directional" type="boolean" truevalue="--non-directional" falsevalue="" checked="false" label="The sequencing library was constructed in a non strand-specific manner, alignments to all four bisulfite strands will be reported."/> + <param argument="--pbat" name="pbat" type="boolean" + truevalue="--pbat" falsevalue="" checked="false" + label="Treat input data as PBAT-Seq libraries" + help="Use this option only if you are certain that your libraries were constructed following a PBAT protocol. If you don't know what PBAT-Seq is you should not specify this option." /> + <!--end output options --> </when> <!-- full --> @@ -544,6 +578,38 @@ <has_text text="--score-min 'L,0,-0.8'" /> </assert_command> </test> + <test> + <param name="genomeSource" value="history"/> + <param name="own_file" value="mm10.tiny.fa.gz" /> + <param name="sPaired" value="single"/> + <param name="input_singles" value="input1.fq.gzip" ftype="fastqsanger.gz"/> + <param name="sort_bam" value="false"/> + <param name="settingsType" value="custom"/> + <param name="suppressed_read_file" value="true"/> + <param name="unmapped_read_file" value="true"/> + <param name="bismark_stdout" value="true"/> + <param name="isReportOutput" value="true"/> + <conditional name="params"> + <param name="settingsType" value="custom" /> + <param name="pbat" value="true" /> + </conditional> + + <output name="output_stdout" file="summary_pbat.txt" ftype="txt" lines_diff="94"> + <assert_contents> + <has_text text="Sequences analysed in total:" /> + <has_text text="44115" /> + <has_text text="Mapping efficiency:" /> + <has_text text="0.0%" /> + <has_text text="Bismark run complete" /> + </assert_contents> + </output> + <output name="report_file" file="mapping_report_pbat.txt" ftype="txt" lines_diff="6"/> + <output name="output" file="mapped_reads_pbat.bam" ftype="qname_input_sorted.bam" lines_diff="14"/> + + <assert_command> + <has_text text="--pbat" /> + </assert_command> + </test> </tests> <help>