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-
- - + #if str($repeat.software) == "fastqc": + ## Searches for files named "fastqc_data.txt" + #for $k, $file in enumerate($repeat.input_file): + mkdir multiqc_WDir/${repeat.software}_${i}/file_${k} && + ln -s '${file}' multiqc_WDir/fastqc_${i}/file_${k}/fastqc_data.txt && + #end for + #else if str($repeat.software) == "tophat": + ## Searches for files ending in "align_summary.txt" + #for $file in $repeat.input_file: + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}align_summary.txt' && + #end for + #else if str($repeat.software) == "bowtie2": + ## Searches for files containing 'reads; of these;' + #for $file in $repeat.input_file: + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' && + #end for + #else if str($repeat.software) == "cutadapt": + ## Searches for files containing 'This is cutadapt' + #for $file in $repeat.input_file: + cat '${file}' > 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' && + ## replace header for old cutadapt release + sed -i .old 's/You are running/This is/' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' && + #end for + #else if str($repeat.software) == "featurecounts": + ## Checks for files ending in '.summary' + #for $file in $repeat.input_file + #if $file.metadata.column_names and $file.metadata.column_names.find(',') != -1 + echo '$file.metadata.column_names.replace(',','\t').replace('__ob__u','').replace('u__sq__','').replace('__sq__','').replace('__cb__','')' >> 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' && + cat '$file' >> 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' && + #else + ln -s '$file' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' && + #end if + #end for + #else if str($repeat.software) == "bismark": + ## Checks for files ending in _SE_report.txt + #for $file in $repeat.input_file + ln -s ${file} 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}_SE_report.txt' && + #end for + #else if str($repeat.software) == "samtools": + ## Checks for files containing 'This file was produced by samtools stats' + #for $file in $repeat.input_file + ln -s ${file} 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' && + #end for + #else if str($repeat.software) == "picard": + #for $file in $repeat.input_file + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' && + #end for + #else if str($repeat.software) == "samtools_idxstats": + ## Checks for files containing "idxstats" in the name + #for $file in $repeat.input_file + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}_idxstats.txt' && + #end for + #else if str($repeat.software) == "htseq": + ## Checks for files containing "__too_low_aQual" + #for $file in $repeat.input_file + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' && + #end for + #else if str($repeat.software) == "rnastar_log": + ## Checks for files named Log.final.out + #for $k, $file in enumerate($repeat.input_file): + mkdir 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' && + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}/Log.final.out' && + #end for + #else if str($repeat.software) == "rnastar_counts": + ## Checks for files named ReadsPerGene.out.tab + #for $k, $file in enumerate($repeat.input_file): + mkdir 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' && + ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}/ReadsPerGene.out.tab' && + #end for + #end if +#end for -
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<tool id="multiqc" name="multiqc" version="@WRAPPER_VERSION@.0">
<description>aggregate results from bioinformatics analyses into a single report</description>
<macros>
<token name="@WRAPPER_VERSION@">1.0.0</token>
</macros>
<requirements>
<requirement type="package" version="@WRAPPER_VERSION@">multiqc</requirement>
</requirements>
<version_command>@WRAPPER_VERSION@</version_command>
<command detect_errors="aggressive">
<![CDATA[
mkdir multiqc_WDir &&
#for $i, $repeat in enumerate( $results )
mkdir multiqc_WDir/${repeat.software}_${i} &&
#if str($repeat.software) == "fastqc":
## Searches for files named "fastqc_data.txt"
#for $k, $file in enumerate($repeat.input_file):
mkdir multiqc_WDir/${repeat.software}_${i}/file_${k} &&
ln -s '${file}' multiqc_WDir/fastqc_${i}/file_${k}/fastqc_data.txt &&
#end for
#else if str($repeat.software) == "tophat":
## Searches for files ending in "align_summary.txt"
#for $file in $repeat.input_file:
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}align_summary.txt' &&
#end for
#else if str($repeat.software) == "bowtie2":
## Searches for files containing 'reads; of these;'
#for $file in $repeat.input_file:
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' &&
#end for
#else if str($repeat.software) == "cutadapt":
## Searches for files containing 'This is cutadapt'
#for $file in $repeat.input_file:
cat '${file}' > 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' &&
## replace header for old cutadapt release
sed -i .old 's/You are running/This is/' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.txt' &&
#end for
#else if str($repeat.software) == "featurecounts":
## Checks for files ending in '.summary'
#for $file in $repeat.input_file
#if $file.metadata.column_names and $file.metadata.column_names.find(',') != -1
echo '$file.metadata.column_names.replace(',','\t').replace('__ob__u','').replace('u__sq__','').replace('__sq__','').replace('__cb__','')' >> 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' &&
cat '$file' >> 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' &&
#else
ln -s '$file' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}.summary' &&
#end if
#end for
#else if str($repeat.software) == "bismark":
## Checks for files ending in _SE_report.txt
#for $file in $repeat.input_file
ln -s ${file} 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}_SE_report.txt' &&
#end for
#else if str($repeat.software) == "samtools":
## Checks for files containing 'This file was produced by samtools stats'
#for $file in $repeat.input_file
ln -s ${file} 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' &&
#end for
#else if str($repeat.software) == "picard":
#for $file in $repeat.input_file
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' &&
#end for
#else if str($repeat.software) == "samtools_idxstats":
## Checks for files containing "idxstats" in the name
#for $file in $repeat.input_file
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}_idxstats.txt' &&
#end for
#else if str($repeat.software) == "htseq":
## Checks for files containing "__too_low_aQual"
#for $file in $repeat.input_file
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' &&
#end for
#else if str($repeat.software) == "rnastar_log":
## Checks for files named Log.final.out
#for $k, $file in enumerate($repeat.input_file):
mkdir 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' &&
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}/Log.final.out' &&
#end for
#else if str($repeat.software) == "rnastar_counts":
## Checks for files named ReadsPerGene.out.tab
#for $k, $file in enumerate($repeat.input_file):
mkdir 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}' &&
ln -s '${file}' 'multiqc_WDir/${repeat.software}_${i}/${file.element_identifier}/ReadsPerGene.out.tab' &&
#end for
#end if
#end for
multiqc multiqc_WDir
]]></command>
<inputs>
<repeat name="results" title="Results" min="1">
<param name="software" type="select" label="Software name" help="Which tool was used generate logs?">
<option value="fastqc">FastQC</option>
<option value="cutadapt">Cutadapt/Trim Galore!</option>
<option value="tophat">Tophat2</option>
<option value="featurecounts">FeatureCounts (Summary file)</option>
<option value="samtools">Samtools (Stats, Flagstat)</option>
<option value="samtools_idxstats">Samtools (Idxstats)</option>
<option value="picard">Picard</option>
<option value="bismark">Bismark</option>
<option value="bowtie2">Bowtie2</option>
<option value="htseq">HTSeq-Count</option>
<option value="rnastar_log">RNA STAR (log)</option>
<option value="rnastar_counts">RNA STAR (reads per gene)</option>
</param>
<param name="input_file" type="data" format="txt, tabular" multiple="true" label="Result file" help="Select input datasets"/>
</repeat>
<param name="saveLog" type="boolean" truevalue="true" falsevalue="false" checked="false" label="Save log file" help="Save the multiQC log file to the history. This is mostly useful for debugging purposes."/>
</inputs>
<outputs>
<data format="html" from_work_dir="multiqc_report.html" name="html_file" label="${tool.name} on ${on_string}: Webpage" />
<data format="txt" name="text_file" from_work_dir="multiqc_data/multiqc.log" label="${tool.name} on ${on_string}: Log">
<filter>saveLog</filter>
</data>
</outputs>
<tests>
<test>
<repeat name="results">
<param name="software" value="fastqc" />
<param name="input_file" value="fastqc_data.txt" />
</repeat>
<param name="saveLog" value="True"/>
<output name="html_file" file="report_fastqc.html" compare="sim_size" delta="1000"/>
<output name="text_file" file="log_fastqc.txt" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="fastqc" />
<param name="input_file" value="fastqc_data.txt,fastqc_data_2.txt" />
</repeat>
<output name="html_file" file="report_fastqc_2.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="cutadapt" />
<param name="input_file" value="cutadapt.txt" />
</repeat>
<output name="html_file" file="report_cutadapt.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="tophat" />
<param name="input_file" value="tophat_data.txt" />
</repeat>
<output name="html_file" file="report_tophat.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="bowtie2" />
<param name="input_file" value="bowtie2SE1.txt,bowtie2SE2.txt" />
</repeat>
<output name="html_file" file="report_bowtie2SE.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="featurecounts" />
<param name="input_file" value="featurecounts_data.txt" />
</repeat>
<output name="html_file" file="report_featurecounts.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="picard" />
<param name="input_file" value="collectGcBias_data.txt,CollectInsertSizeMetrics.txt,MarkDuplicates_data.txt,picard_CollectBaseDistributionByCycle.txt,picard_CollectRnaSeqMetrics.txt,picard_CollectAlignmentSummaryMetrics.txt" />
</repeat>
<output name="html_file" file="report_picard.html" compare="sim_size" delta="10000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="htseq" />
<param name="input_file" value="htseq_data.txt" />
</repeat>
<output name="html_file" file="report_htseq.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="rnastar_log" />
<param name="input_file" value="rnastar_log.txt" />
</repeat>
<output name="html_file" file="report_rnastar_log.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="rnastar_counts" />
<param name="input_file" value="rnastar_counts.txt" />
</repeat>
<output name="html_file" file="report_rnastar_counts.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="bismark" />
<param name="input_file" value="bismark_data.txt" />
</repeat>
<output name="html_file" file="report_bismark.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="samtools" />
<param name="input_file" value="samtools_stats.txt,samtools_flagstat.txt" />
</repeat>
<output name="html_file" file="report_samtools.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="samtools_idxstats" />
<param name="input_file" value="samtools_idxstats.txt" />
</repeat>
<output name="html_file" file="report_samtools_idxstats.html" compare="sim_size" delta="1000"/>
</test>
<test>
<repeat name="results">
<param name="software" value="fastqc" />
<param name="input_file" value="fastqc_data.txt,fastqc_data_2.txt" />
</repeat>
<repeat name="results">
<param name="software" value="cutadapt" />
<param name="input_file" value="cutadapt.txt" />
</repeat>
<repeat name="results">
<param name="software" value="tophat" />
<param name="input_file" value="tophat_data.txt" />
</repeat>
<repeat name="results">
<param name="software" value="featurecounts" />
<param name="input_file" value="featurecounts_data.txt" />
</repeat>
<repeat name="results">
<param name="software" value="picard" />
<param name="input_file" value="collectGcBias_data.txt,CollectInsertSizeMetrics.txt,MarkDuplicates_data.txt" />
</repeat>
<repeat name="results">
<param name="software" value="bismark" />
<param name="input_file" value="bismark_data.txt" />
</repeat>
<repeat name="results">
<param name="software" value="samtools" />
<param name="input_file" value="samtools_stats.txt,samtools_flagstat.txt" />
</repeat>
<output name="html_file" file="report_all.html" compare="sim_size" delta="5000"/>
</test>
</tests>
-
<help><![CDATA[
**What it does**
MultiQC aggregates results from bioinformatics analyses across many samples into a single report. It takes results of multiple analyses and creates a report that can be viewed as a single beautiful web-page. It's a general use tool, perfect for summarizing the output from numerous bioinformatics tools.
**Inputs**
MultiQC takes software output summaries/logs and creates a single report from them. You need to tell the tool which software was used to generate the report. This is done using the **Software name** dropdown. At present the following Galaxy tools produce logs that can used with MultiQC. There are:
- Fastqc
- Cutadapt / Trim Galore!
- Tophat2
- FeatureCounts (summary file with the column header in the first line or as metadata)
- Samtools (stats, flagstat, dxstats)
- Picard (MarkDuplicatesMetrics, CollectGCBiasMetrics, CollectInsertSizeMetrics, CollectAlignmentSummaryMetrics, CollectRnaSeqMetrics)
- Bismark (Alignment report file)
- Bowtie2 (Metrics file)
- HTSeq-count ("no feature" file; although the "Assigned" metric is always 0)
- RNA STAR (Alignment from Log.final.out, Gene counts from ReadsPerGene.out.tab)
----
**Integrated by**
Cyril Monjeaud and Yvan Le Bras
`EnginesOn &lt;http://engineson.fr/&gt;`_ and Rennes GenOuest Bio-informatics Core Facility
]]></help>
<citations>
<citation type="doi">10.1093/bioinformatics/btw354</citation>
</citations>
</tool>
+multiqc multiqc_WDir + ]]> + + + + + + + + + + + + + + + + + + + + + + + + saveLog + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + -
- -
- - - - -
- -
+ -
- -
+MultiQC aggregates results from bioinformatics analyses across many samples into a single report. It takes results of multiple analyses and creates a report that can be viewed as a single beautiful web-page. It's a general use tool, perfect for summarizing the output from numerous bioinformatics tools. - - - - - -
- - - You can't perform that action at this time. -
- +- Fastqc +- Cutadapt / Trim Galore! +- Tophat2 +- FeatureCounts (summary file with the column header in the first line or as metadata) +- Samtools (stats, flagstat, dxstats) +- Picard (MarkDuplicatesMetrics, CollectGCBiasMetrics, CollectInsertSizeMetrics, CollectAlignmentSummaryMetrics, CollectRnaSeqMetrics) +- Bismark (Alignment report file) +- Bowtie2 (Metrics file) +- HTSeq-count ("no feature" file; although the "Assigned" metric is always 0) +- RNA STAR (Alignment from Log.final.out, Gene counts from ReadsPerGene.out.tab) - - - - - - - - -
- - You signed in with another tab or window. Reload to refresh your session. - You signed out in another tab or window. Reload to refresh your session. -
- +---- + +**Integrated by** + +Cyril Monjeaud and Yvan Le Bras +`EnginesOn <http://engineson.fr/>`_ and Rennes GenOuest Bio-informatics Core Facility - - - + ]]> + + 10.1093/bioinformatics/btw354 + +