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author | iuc |
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date | Thu, 10 Aug 2017 06:37:09 -0400 |
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<tool id="umi_tools_extract" name="UMI-tools extract" version="0.4.4.0"> <description>Extract UMI from fastq files</description> <requirements> <requirement type="package" version="0.4.4">umi_tools</requirement> </requirements> <command detect_errors="exit_code"><![CDATA[ #set $gz = False #if $input_type.type == 'single': #if $input_type.input_single.is_of_type("fastq.gz", "fastqsanger.gz"): ln -s '$input_type.input_single' input_single.gz && #set $gz = True #end if #else #if $input_type.input_read1.is_of_type("fastq.gz", "fastqsanger.gz"): ln -s '$input_type.input_read1' input_read1.gz && ln -s '$input_type.input_read2' input_read2.gz && #set $gz = True #end if #end if umi_tools extract --bc-pattern='$bc_pattern' #if $input_type.type == 'single': #if $gz: --stdin=input_single.gz --stdout out.gz #else --stdin='$input_type.input_single' --stdout '$out' #end if #else: #if $gz: --stdin=input_read1.gz --read2-in=input_read2.gz --stdout out1.gz --read2-out=out2.gz #else: --stdin='$input_type.input_read1' --read2-in='$input_type.input_read2' --stdout '$out1' --read2-out='$out2' #end if #if $input_type.barcode.split == "1": --split-barcode --bc-pattern2='$input_type.barcode.bc_pattern2' #end if #end if #if not $prime3: --3prime #end if #if $quality.quality_selector =='true': --quality-filter-threshold '$quality.quality_filter_threshold' --quality-encoding '$quality.quality_encoding' #end if #if $print_log == "1": --log='$out_log' #else --supress-stats #end if #if $gz: #if $input_type.type == 'single': && mv out.gz '$out' #else && mv out1.gz '$out1' && mv out2.gz '$out2' #end if #end if ]]></command> <inputs> <conditional name="input_type"> <param name="type" type="select" label="Library type"> <option value="single">Single-end</option> <option value="paired">Paired-end</option> </param> <when value="single"> <param name="input_single" type="data" format="fastq,fastq.gz" label="Reads in FASTQ format" /> </when> <when value="paired"> <param name="input_read1" type="data" format="fastq,fastq.gz" label="Reads in FASTQ format" /> <param name="input_read2" type="data" format="fastq,fastq.gz" label="Reads in FASTQ format" /> <conditional name="barcode"> <param name="split" argument="--split-barcode" type="select" label="Barcode on both reads?"> <option value="0">Barcode on first read only</option> <option value="1">Barcode on both reads</option> </param> <when value="0"> </when> <when value="1"> <param name="bc_pattern2" argument="--bc-pattern2" type="text" value="" label="Barcode pattern for second read" help="Use this option to specify the format of the UMI/barcode for the second read pair if required."> </param> </when> </conditional> </when> </conditional> <param name="bc_pattern" argument="--bc-pattern" type="text" label="Barcode pattern for first read" help="Use this option to specify the format of the UMI/barcode. Use Ns to represent the random positions and Xs to indicate the bc positions. Bases with Ns will be extracted and added to the read name. Remaining bases, marked with an X will be reattached to the read."> </param> <param name="prime3" argument="--3prime" type="boolean" label="Is the barcode at the 5' end?" truevalue="1" falsevalue="0" checked="true" help="By default the barcode is assumed to be on the 5' end of the read, but use this option to sepecify that it is on the 3' end instead." /> <param name="print_log" argument="-L" type="boolean" label="Output log?" truevalue="1" falsevalue="0" checked="true" help="Choose if you want to generate a text file containing logging information." /> <conditional name="quality"> <param name="quality_selector" type="select" label="Enable quality filter?" > <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false"> </when> <when value="true"> <param name="quality_filter_threshold" label="Phred score threshold" type="integer" value="20" argument="--quality-filter-threshold" help="Remove reads where any UMI base quality score falls below this threshold." /> <param name="quality_encoding" argument="--quality-encoding" type="select" label="Library type" help="Quality score encoding. Choose from phred33 [33-77], phred64 [64-106] or solexa [59-106]."> <option value="phred33">phred33 [33-77]</option> <option value="phred64">phred64 [64-106]</option> <option value="solexa">solexa [59-106]</option> </param> </when> </conditional> </inputs> <outputs> <data name="out" format_source="input_single"> <filter>input_type['type'] == "single"</filter> </data> <data name="out1" format_source="input_read1"> <filter>input_type['type'] == "paired"</filter> </data> <data name="out2" format_source="input_read2"> <filter>input_type['type'] == "paired"</filter> </data> <data name="out_log" format="txt"> <filter>print_log == True</filter> </data> </outputs> <tests> <test> <param name="type" value="single" /> <param name="input_single" value="t_R1.fastq" ftype="fastq" /> <param name="bc_pattern" value="XXXNNN" /> <param name="prime3" value="0" /> <param name="quality_selector" value="true" /> <param name="quality_filter_threshold" value="10" /> <param name="quality_encoding" value="phred33" /> <output name="out" file="out_SE.fastq" /> <output name="out_log" file="out_single.log" lines_diff="15"/> </test> <test> <param name="type" value="paired" /> <param name="input_read1" value="t_R1.fastq.gz" ftype="fastq.gz" /> <param name="input_read2" value="t_R2.fastq.gz" ftype="fastq.gz" /> <param name="bc_pattern" value="NNNXXX" /> <output name="out1" file="out_R1.fastq.gz" decompress="true" /> <output name="out2" file="out_R2.fastq.gz" decompress="true" /> <output name="out_log" file="out_paired.log" lines_diff="10"/> </test> </tests> <help><![CDATA[ UMI-tools extract.py - Extract UMI from fastq ============================================= Purpose ------- Extract UMI barcode from a read and add it to the read name, leaving any sample barcode in place. Can deal with paired end reads and UMIs split across the paired ends Options ------- --split-barcode By default the UMI is assumed to be on the first read. Use this option if the UMI is contained on both reads and specify the pattern of the barcode/UMI on the second read using the option ``--bc-pattern2`` --bc-pattern Use this option to specify the format of the UMI/barcode. Use Ns to represent the random positions and Xs to indicate the bc positions. Bases with Ns will be extracted and added to the read name. Remaining bases, marked with an X will be reattached to the read. E.g. If the pattern is NNXXNN, Then the read: @HISEQ:87:00000000 read1 AAGGTTGCTGATTGGATGGGCTAG DA1AEBFGGCG01DFH00B1FF0B + will become: @HISEQ:87:00000000_AATT read1 GGGCTGATTGGATGGGCTAG 1AFGGCG01DFH00B1FF0B + --bc-pattern2 Use this option to specify the format of the UMI/barcode for the second read pair if required. If --bc-pattern2 is not supplied, this defaults to the same pattern as --bc-pattern --3prime By default the barcode is assumed to be on the 5' end of the read, but use this option to sepecify that it is on the 3' end instead -L Specify a log file to retain logging information and final statistics --split-barcode barcode is split across read pair --quality-filter-threshold=QUALITY_FILTER_THRESHOLD Remove reads where any UMI base quality score falls below this threshold --quality-encoding=QUALITY_ENCODING Quality score encoding. Choose from phred33[33-77] phred64 [64-106] or solexa [59-106] Usage: ------ For single ended reads: umi_tools extract --bc-pattern=[PATTERN] -L extract.log [OPTIONS] reads from stdin and outputs to stdout. For paired end reads: umi_tools extract --bc-pattern=[PATTERN] --read2-in=[FASTQIN] --read2-out=[FASTQOUT] -L extract.log [OPTIONS] reads end one from stdin and end two from FASTQIN and outputs end one to stdin and end two to FASTQOUT. ]]></help> <citations> <citation type="doi">10.1101/gr.209601.116</citation> <citation type="bibtex"> @misc{githubUMI-tools, title = {UMI-tools}, publisher = {GitHub}, journal = {GitHub repository}, url = {https://github.com/CGATOxford/UMI-tools}, } </citation> </citations> </tool>