Mercurial > repos > triasteran > ribogalaxy_umi_processing
view UMI_riboseq_processing/UMI_riboseq.xml @ 9:31438c26afec draft
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author | triasteran |
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date | Tue, 21 Jun 2022 14:41:24 +0000 |
parents | 701804f5ad4b |
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<tool id="UMI_riboseq" name="move UMIs from reads to header" version="0.1.6d"> <requirements> <requirement type="package" version="1.75">biopython</requirement> </requirements> <command detect_errors="exit_code"> <![CDATA[ python3 '$__tool_directory__/UMI.py' $reads $output ]]> </command> <inputs> <param format="fastqsanger,fastqsanger.gz" name="reads" type="data" label="fastqsanger,fastqsanger.gz"/> </inputs> <outputs> <data format="fastqsanger" name="output"/> </outputs> <tests> <test> <param name="reads" value="sub_10k_reads.fq.gz"/> <output name="output" file="output"/> </test> <test> <param name="reads" value="sub_10k_reads2.fq"/> <output name="output" file="output2"/> </test> </tests> <help> <![CDATA[ fastq/fastq.gz are input files with reads containing UMIs (already demultiplexed and adapters are removed). The output of the script is fastq/fastq.gz file where UMIs (7nt in total, 5'NN and 3'NNNNN preceding barcode consisting of 5nt) are in header of the read. It is designed for protocol: McGlincy NJ, Ingolia NT. Transcriptome-wide measurement of translation by ribosome profiling. Methods. 2017;126:112-129. doi:10.1016/j.ymeth.2017.05.028 ]]> </help> <citations> <citation type="bibtex"> @misc{FedorovaAD2022, author = {Fedorova Alla}, year = {2022}, title = {UMI_for_riboseq}, publisher = {GitHub}, journal = {GitHub repository}, url = {https://github.com/triasteran/RiboGalaxy_with_ansible/blob/main/toolshed_tools/UMI_riboseq_tool/UMI.py}, } </citation> </citations> </tool>