Mercurial > repos > iuc > bctools_merge_pcr_duplicates
view merge_pcr_duplicates.xml @ 2:067139d6fc88 draft default tip
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bedtools commit 758b42538f722759e7b5414f64c9a7973cc221b4"
author | iuc |
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date | Wed, 25 Dec 2019 11:40:16 -0500 |
parents | daad7189e48e |
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<tool id="bctools_merge_pcr_duplicates" name="Merge PCR duplicates" version="@VERSION@+galaxy1"> <description>according to UMIs</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"> <requirement type="package" version="8.31">coreutils</requirement> </expand> <command detect_errors="exit_code"><![CDATA[ merge_pcr_duplicates.py '$alignments_bed' '$barcode_library' --outfile '$events' ]]></command> <inputs> <param name="alignments_bed" type="data" format="bed" label="BED6 file containing alignments" /> <param name="barcode_library" type="data" format="fastq" label="FASTQ barcode library" /> </inputs> <outputs> <data name="events" format="bed"/> </outputs> <tests> <test> <param name="alignments_bed" value="pcr_dupes_sorted_2.bed"/> <param name="barcode_library" value="pcr_dupes_randomdict.fastq"/> <output name="events" file="merged_pcr_dupes.bed"/> </test> </tests> <help><![CDATA[ bctools - Merge PCR duplicates according to UMIs ================================================ Merge PCR duplicates according to unique molecular identifier (UMI) library. All alignments with same outer coordinates and barcode will be merged into a single crosslinking event. Barcodes containing uncalled base 'N' are removed. Input: ------ * BED6 file containing alignments with FASTQ read-id in name field * FASTQ library of UMIs Output: ------- * BED6 file with a read id from a representative alignment in the name field and number of PCR duplicates as score, sorted by fields chrom, start, stop, strand, name ]]></help> <expand macro="citations"/> </tool>