Mercurial > repos > iuc > sinto_barcode
comparison sinto_barcode.xml @ 0:3456ec59ff7a draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sinto commit a836e4e010093207186d4d7839bbba702a15c18f
| author | iuc |
|---|---|
| date | Thu, 13 Apr 2023 11:03:17 +0000 |
| parents | |
| children | f1d83e3a2357 |
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| -1:000000000000 | 0:3456ec59ff7a |
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| 1 <tool id="sinto_barcode" name="Sinto barcode" profile="20.01" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@"> | |
| 2 <description>add cell barcodes to FASTQ read names</description> | |
| 3 <macros> | |
| 4 <import>macros.xml</import> | |
| 5 </macros> | |
| 6 <requirements> | |
| 7 <requirement type="package" version="@TOOL_VERSION@">sinto</requirement> | |
| 8 </requirements> | |
| 9 <version_command>sinto --version</version_command> | |
| 10 <command><![CDATA[ | |
| 11 ln -s '$barcode_fastq' barcodes.fastq.gz && | |
| 12 ln -s '${fastq_input.read1_fastq}' read1.fastq.gz && | |
| 13 #if str( $fastq_input.fastq_input_selector ) == "paired": | |
| 14 ln -s '${fastq_input.read2_fastq}' read2.fastq.gz && | |
| 15 #end if | |
| 16 sinto barcode | |
| 17 --barcode_fastq barcodes.fastq.gz | |
| 18 --read1 read1.fastq.gz | |
| 19 #if str( $fastq_input.fastq_input_selector ) == "paired": | |
| 20 --read2 read2.fastq.gz | |
| 21 #end if | |
| 22 --bases $bases | |
| 23 ]]> </command> | |
| 24 <inputs> | |
| 25 <param type="data" name="barcode_fastq" format="fastqsanger.gz" label="FASTQ file containing cell barcode sequences" /> | |
| 26 <conditional name="fastq_input"> | |
| 27 <param name="fastq_input_selector" type="select" label="Single or Paired-end data"> | |
| 28 <option value="paired">Paired</option> | |
| 29 <option value="single">Single</option> | |
| 30 </param> | |
| 31 <when value="paired"> | |
| 32 <param name="read1_fastq" type="data" format="fastqsanger.gz" label="Forward reads FASTQ file" /> | |
| 33 <param name="read2_fastq" type="data" format="fastqsanger.gz" label="Reverse reads FASTQ file" /> | |
| 34 </when> | |
| 35 <when value="single"> | |
| 36 <param name="read1_fastq" type="data" format="fastqsanger.gz" label="Select FASTQ file" /> | |
| 37 </when> | |
| 38 </conditional> | |
| 39 <param type="integer" name="bases" value="16" min="0" label="Number of bases to extract from barcode-containing FASTQ" /> | |
| 40 </inputs> | |
| 41 <outputs> | |
| 42 <data name='read1_out' format='fastqsanger.gz' label="${tool.name} on ${on_string}: barcoded read 1" from_work_dir="read1.barcoded.fastq" /> | |
| 43 <data name='read2_out' format='fastqsanger.gz' label="${tool.name} on ${on_string}: barcoded read 2" from_work_dir="read2.barcoded.fastq" > | |
| 44 <filter>fastq_input['fastq_input_selector'] == 'paired'</filter> | |
| 45 </data> | |
| 46 </outputs> | |
| 47 <tests> | |
| 48 <test expect_num_outputs="1"> | |
| 49 <param name="barcode_fastq" value="barcodes.fastq.gz" /> | |
| 50 <param name="fastq_input_selector" value="single"/> | |
| 51 <param name="read1_fastq" value="read1.fastq.gz" /> | |
| 52 <output name="read1_out" file="read1.barcoded.fastq.gz" ftype="fastqsanger.gz" decompress="true" /> | |
| 53 </test> | |
| 54 <test expect_num_outputs="2"> | |
| 55 <param name="barcode_fastq" value="barcodes.fastq.gz" /> | |
| 56 <param name="fastq_input_selector" value="paired"/> | |
| 57 <param name="read1_fastq" value="read1.fastq.gz" /> | |
| 58 <param name="read2_fastq" value="read2.fastq.gz" /> | |
| 59 <output name="read1_out" file="read1.barcoded.fastq.gz" ftype="fastqsanger.gz" decompress="true"/> | |
| 60 <output name="read2_out" file="read2.barcoded.fastq.gz" ftype="fastqsanger.gz" decompress="true"/> | |
| 61 </test> | |
| 62 </tests> | |
| 63 <help><![CDATA[ | |
| 64 | |
| 65 Sinto is a toolkit for processing aligned single-cell data. | |
| 66 -------------------------------------------------------------------------------------------------------------- | |
| 67 Cell barcodes from one FASTQ file added to the read names of another, or the same, FASTQ file. This is useful when processing raw single-cell sequencing data, as the cell barcode information can easily be propagated to the aligned BAM file by encoding the cell barcode in the read name. | |
| 68 | |
| 69 **Inputs** | |
| 70 FASTQ files containing barcodes and forward reads. An optional reverse reads FASTQ file can be provided for paired-end experiments. Note that all the FASTQs must contain the same number of reads and the reads must appear in the same order. | |
| 71 | |
| 72 **Outputs** | |
| 73 FASTQ files with the read names modified to contain the cell barcode sequence at the beginning of the read name, separated from the original read name by a : character. | |
| 74 | |
| 75 ]]> </help> | |
| 76 <expand macro="citations" /> | |
| 77 </tool> |
