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view qiime2/qiime_cutadapt_demux-single.xml @ 3:558645416841 draft
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author | florianbegusch |
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date | Sun, 21 Jul 2019 02:21:34 -0400 |
parents | 51025741f326 |
children | 914fa4daf16a |
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<?xml version="1.0" ?> <tool id="qiime_cutadapt_demux-single" name="qiime cutadapt demux-single" version="2019.4"> <description> - Demultiplex single-end sequence data with barcodes in- sequence.</description> <requirements> <requirement type="package" version="2019.4">qiime2</requirement> </requirements> <command><![CDATA[ qiime cutadapt demux-single --i-seqs=$iseqs --m-barcodes-column="$mbarcodescolumn" --o-per-sample-sequences=opersamplesequences --o-untrimmed-sequences=ountrimmedsequences #if $input_files_mbarcodesfile: #def list_dict_to_string(list_dict): #set $file_list = list_dict[0]['additional_input'].__getattr__('file_name') #for d in list_dict[1:]: #set $file_list = $file_list + ',' + d['additional_input'].__getattr__('file_name') #end for #return $file_list #end def --m-barcodes-file=$list_dict_to_string("$input_files_mbarcodesfile") #end if #if $perrorrate: --p-error-rate=$perrorrate #end if ; cp opersamplesequences.qza $opersamplesequences; cp ountrimmedsequences.qza $ountrimmedsequences ]]></command> <inputs> <param format="qza,no_unzip.zip" label="--i-seqs: ARTIFACT MultiplexedSingleEndBarcodeInSequence The single-end sequences to be demultiplexed. [required]" name="iseqs" optional="False" type="data"/> <repeat name="$input_files_mbarcodesfile" optional="False" title="--m-barcodes-file"> <param label="--m-barcodes-file: Metadata file or artifact viewable as metadata. This option may be supplied multiple times to merge metadata. [required]" name="additional_input" type="data" format="tabular,qza,no_unzip.zip" /> </repeat> <param label="--m-barcodes-column: COLUMN MetadataColumn[Categorical] The sample metadata column listing the per-sample barcodes. [required]" name="mbarcodescolumn" optional="False" type="text"/> <param label="--p-error-rate: PROPORTION Range(0, 1, inclusive_end=True) The level of error tolerance, specified as the maximum allowable error rate. The default value specified by cutadapt is 0.1 (=10%), which is greater than `demux emp-*`, which is 0.0 (=0%). [default: 0.1]" name="perrorrate" optional="True" type="float" min="0" max="1" exclude_max="False" value="0.1"/> </inputs> <outputs> <data format="qza" label="${tool.name} on ${on_string}: persamplesequences.qza" name="opersamplesequences"/> <data format="qza" label="${tool.name} on ${on_string}: untrimmedsequences.qza" name="ountrimmedsequences"/> </outputs> <help><![CDATA[ Demultiplex single-end sequence data with barcodes in-sequence. ############################################################### Demultiplex sequence data (i.e., map barcode reads to sample ids). Barcodes are expected to be located within the sequence data (versus the header, or a separate barcode file). Parameters ---------- seqs : MultiplexedSingleEndBarcodeInSequence The single-end sequences to be demultiplexed. barcodes : MetadataColumn[Categorical] The sample metadata column listing the per-sample barcodes. error_rate : Float % Range(0, 1, inclusive_end=True), optional The level of error tolerance, specified as the maximum allowable error rate. The default value specified by cutadapt is 0.1 (=10%), which is greater than `demux emp-*`, which is 0.0 (=0%). Returns ------- per_sample_sequences : SampleData[SequencesWithQuality] The resulting demultiplexed sequences. untrimmed_sequences : MultiplexedSingleEndBarcodeInSequence The sequences that were unmatched to barcodes. ]]></help> <macros> <import>qiime_citation.xml</import> </macros> <expand macro="qiime_citation"/> </tool>